-
1
-
-
0021799672
-
Rarer quantitative and qualitative abnormalities of coagulation
-
Girolami, A., De Marco, L., Dal Bo Zanon, R., Patrassi, R., Cappellato, M. G. Rarer quantitative and qualitative abnormalities of coagulation. Clin Hematol 1985; 14: 385-411.
-
(1985)
Clin Hematol
, vol.14
, pp. 385-411
-
-
Girolami, A.1
de Marco, L.2
Dal Bo Zanon, R.3
Patrassi, R.4
Cappellato, M.G.5
-
2
-
-
0022618575
-
Coagulation disorders in the neonate
-
Buchanan, G.R. Coagulation disorders in the neonate. Pediatr Clin North Am 1986; 33: 203-220.
-
(1986)
Pediatr Clin North Am
, vol.33
, pp. 203-220
-
-
Buchanan, G.R.1
-
3
-
-
0021891210
-
Newborn haemostasis
-
Montgomery, R. R., Marlar, R. A., Gill, J. C. Newborn haemostasis. Clin Hematol 1985; 14: 443-460.
-
(1985)
Clin Hematol
, vol.14
, pp. 443-460
-
-
Montgomery, R.R.1
Marlar, R.A.2
Gill, J.C.3
-
4
-
-
0024583675
-
Neonatal haemostasis
-
Gibson, B. Neonatal haemostasis. Arch Dis Child 1989; 64: 503-506.
-
(1989)
Arch Dis Child
, vol.64
, pp. 503-506
-
-
Gibson, B.1
-
5
-
-
0026562062
-
Further evidence for recessive inheritance of von willebrand disease with abnormal binding of von willebrand factor to factor viii
-
Lopez-Fernandez, M. F., Blanco-Lopez, M. J., Castineira, M. P, Batlle, J. Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII. Am J Hematol 1992; 40: 20-27.
-
(1992)
Am J Hematol
, vol.40
, pp. 20-27
-
-
Lopez-Fernandez, M.F.1
Blanco-Lopez, M.J.2
Castineira, M.P.3
Batlle, J.4
-
6
-
-
0027537705
-
Recessive inheritance of von willebrand’s disease type i
-
Eikenboom, J. C., Reitsma, P H., Peerlinck, K. M., Briet, E. Recessive inheritance of von Willebrand’s disease type I. Lancet 1993; 341: 982-986.
-
(1993)
Lancet
, vol.341
, pp. 982-986
-
-
Eikenboom, J.C.1
Reitsma, P.H.2
Peerlinck, K.M.3
Briet, E.4
-
7
-
-
0020378050
-
Combined congenital deficiency of factor v and factor viii
-
Mazzone, D., Fichera, A., Pratico, G., Sciacca, F. Combined congenital deficiency of factor V and factor VIII. Acta Haematol 1982; 68: 337-338.
-
(1982)
Acta Haematol
, vol.68
, pp. 337-338
-
-
Mazzone, D.1
Fichera, A.2
Pratico, G.3
Sciacca, F.4
-
8
-
-
0014009563
-
Congenital combined deficiency of coagulation factors ii, vii, ix and x
-
McMillan, C., Roberts, H. Congenital combined deficiency of coagulation factors II, VII, IX and X. N Engl J Med 1966; 274: 1313-1315.
-
(1966)
N Engl J Med
, vol.274
, pp. 1313-1315
-
-
McMillan, C.1
Roberts, H.2
-
9
-
-
0000025783
-
Intracranial bleeding in hemophilia
-
Silverstein, A. Intracranial bleeding in hemophilia. Arch Neurol 1960; 3:141-157.
-
(1960)
Arch Neurol
, vol.3
, pp. 141-157
-
-
Silverstein, A.1
-
10
-
-
0023676464
-
Intracranial haemorrhage in newborn and young infants with hemophilia
-
Yoffe, G., Buchanan, G. R. Intracranial haemorrhage in newborn and young infants with hemophilia. J Pediatr 1988;113:333-336.
-
(1988)
J Pediatr
, vol.113
, pp. 333-336
-
-
Yoffe, G.1
Buchanan, G.R.2
-
11
-
-
0023865306
-
Intracranial hemorrhage in congenital deficiency of factor xiii
-
Abbondanzo, S. L., Gootenberg, J. E., Lofts, R. S., McPherson, R. A. Intracranial hemorrhage in congenital deficiency of factor XIII. Am J Pediatr Hematol Oncol 1988; 10: 65-68.
-
(1988)
Am J Pediatr Hematol Oncol
, vol.10
, pp. 65-68
-
-
Abbondanzo, S.L.1
Gootenberg, J.E.2
Lofts, R.S.3
McPherson, R.A.4
-
12
-
-
84979448020
-
Intracranial hemorrhage and occlusive hydrocephalus in hereditary bleeding disorders
-
Struwe, F. Intracranial hemorrhage and occlusive hydrocephalus in hereditary bleeding disorders. Dev Med Child Neurol 1970; 12:165-169.
-
(1970)
Dev Med Child Neurol
, vol.12
, pp. 165-169
-
-
Struwe, F.1
-
13
-
-
0020552654
-
Factor vii congenital deficiency: Clinical picture and classification of the variants
-
Mariani, G., Mazzucconi, M. G. Factor VII congenital deficiency: clinical picture and classification of the variants. Haemostasis 1983; 13: 169-177.
-
(1983)
Haemostasis
, vol.13
, pp. 169-177
-
-
Mariani, G.1
Mazzucconi, M.G.2
-
14
-
-
0014009008
-
Hemophilia in the first year of life
-
Baehner, R. L., Strauss, H. Hemophilia in the first year of life. N Engl J Med 1966; 275: 524-528.
-
(1966)
N Engl J Med
, vol.275
, pp. 524-528
-
-
Baehner, R.L.1
Strauss, H.2
-
15
-
-
0014964632
-
Gilbert syndrome and factor-vii deficiency
-
Seligsohn, U., Shani, M., Ramot, B. Gilbert syndrome and factor-VII deficiency. Lancet 1970; 1:1398.
-
(1970)
Lancet
, vol.1
, pp. 1398
-
-
Seligsohn, U.1
Shani, M.2
Ramot, B.3
-
16
-
-
0015450410
-
Active and inactive factor vii in dubin-johnson syndrome with factor-vii deficiency, hereditary factor-vii deficiency and on coumadin administration
-
Levanon, M., Rimon, S., Shani, M., Ramot, B., Goldberg, E. Active and inactive factor VII in Dubin-Johnson syndrome with factor-VII deficiency, hereditary factor-VII deficiency and on coumadin administration. Br J Haematol 1972; 23: 669-677.
-
(1972)
Br J Haematol
, vol.23
, pp. 669-677
-
-
Levanon, M.1
Rimon, S.2
Shani, M.3
Ramot, B.4
Goldberg, E.5
-
17
-
-
0023179188
-
Development of the human coagulation system in the full-term infant
-
Andrew, M., Paes, B., Milner, R., et al. Development of the human coagulation system in the full-term infant. Blood 1987;70:165-172.
-
(1987)
Blood
, vol.70
, pp. 165-172
-
-
Andrew, M.1
Paes, B.2
Milner, R.3
-
18
-
-
0023787137
-
Development of the human coagulation system in the healthy premature infant
-
Andrew, M., Paes, B., Milner, R., et al. Development of the human coagulation system in the healthy premature infant. Blood 1988; 72:1651-1657.
-
(1988)
Blood
, vol.72
, pp. 1651-1657
-
-
Andrew, M.1
Paes, B.2
Milner, R.3
-
19
-
-
0025266246
-
Development of the hemostatic system in the neonate and young infant
-
Andrew, M., Paes, B., Johnston, M. Development of the hemostatic system in the neonate and young infant. Am J PediatrHematol Oncol 1990; 12:95-104.
-
(1990)
Am J Pediatrhematol Oncol
, vol.12
, pp. 95-104
-
-
Andrew, M.1
Paes, B.2
Johnston, M.3
-
20
-
-
0023188726
-
Effect of ethanolon thromboxane and prostacyclin synthesisbyfetal platelets and umbilical artery
-
Ylikorkala, O., Halmesmaki, E., Viinikka, L. Effect of ethanolon thromboxane and prostacyclin synthesisbyfetal platelets and umbilical artery. Life Sci 1987; 41: 371-376.
-
(1987)
Life Sci
, vol.41
, pp. 371-376
-
-
Ylikorkala, O.1
Halmesmaki, E.2
Viinikka, L.3
-
21
-
-
0022549943
-
Prenatal diagnosis of hemophilia by fetal blood sampling under ultrasound guidance
-
Forestier, F, Daffos, F, Sole, Y., Rainaut, M. Prenatal diagnosis of hemophilia by fetal blood sampling under ultrasound guidance. Haemostasis 1986; 16:346-351.
-
(1986)
Haemostasis
, vol.16
, pp. 346-351
-
-
Forestier, F.1
Daffos, F.2
Sole, Y.3
Rainaut, M.4
-
22
-
-
0032851869
-
Prenatal diagnosis in factor xiii-a deficiency
-
Killick, C. J., Barton, C. J., Aslam, S., Standen, G. Prenatal diagnosis in factor XIII-A deficiency. Arch Dis Child Fetal NeonatalEd 1999; 80: F238-F239.
-
(1999)
Arch Dis Child Fetal Neonataled
, vol.80
, pp. F238-F239
-
-
Killick, C.J.1
Barton, C.J.2
Aslam, S.3
Standen, G.4
-
23
-
-
0021853114
-
Prenatal diagnosis of haemophilia a by factor viii gene analysis
-
Antonarakis, S. E., Copeland, K. L., Carpenter, R. J., etal.Prenatal diagnosis of haemophilia A by factor VIII gene analysis. Lancet 1985; 1: 1407-1409.
-
(1985)
Lancet
, vol.1
, pp. 1407-1409
-
-
Antonarakis, S.E.1
Copeland, K.L.2
Carpenter, R.J.3
-
24
-
-
0025183086
-
Family studies and prenataldiagnosisinseverevonwillebranddiseasebypoly- merase chain reaction amplification of a variable number tandem repeat region of the von willebrand factor gene
-
Peake, I. R., Bowen, D., Bignell, P., et al. Family studies and prenataldiagnosisinseverevonWillebranddiseasebypoly- merase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene. Blood 1990; 76: 555-561.
-
(1990)
Blood
, vol.76
, pp. 555-561
-
-
Peake, I.R.1
Bowen, D.2
Bignell, P.3
-
25
-
-
73849161717
-
Pediatric aspects of the mild hemophilias
-
Schulman, I. Pediatric aspects of the mild hemophilias. Med Clin NorthAm 1962; 46: 93-105.
-
(1962)
Med Clin Northam
, vol.46
, pp. 93-105
-
-
Schulman, I.1
-
26
-
-
0006028937
-
Massive hemorrhage: Scalps of newborn infants
-
Kozinn, P., Ritz, N., Moss, A., Kaufman, A. Massive hemorrhage: scalps of newborn infants. Am J Dis Child 1964; 108: 413-417.
-
(1964)
Am J Dis Child
, vol.108
, pp. 413-417
-
-
Kozinn, P.1
Ritz, N.2
Moss, A.3
Kaufman, A.4
-
27
-
-
0006063839
-
Scalp hemorrhage as an emergency in the newborn
-
Kozinn, P., Ritz, N., Horowitz, A. Scalp hemorrhage as an emergency in the newborn. J Am Med Assoc 1965; 194: 179-180.
-
(1965)
J am Med Assoc
, vol.194
, pp. 179-180
-
-
Kozinn, P.1
Ritz, N.2
Horowitz, A.3
-
28
-
-
0015536669
-
Intracranial hemorrhage and subsequent communicating hydrocephalus in a neonate with classical hemophilia
-
McCarthy, J., Coble, L. Intracranial hemorrhage and subsequent communicating hydrocephalus in a neonate with classical hemophilia. J Pediatr 1973; 51:122-124.
-
(1973)
J Pediatr
, vol.51
, pp. 122-124
-
-
McCarthy, J.1
Coble, L.2
-
29
-
-
0023637240
-
Hemophilia presenting with intracranial hemorrhage
-
Bray, G. L., Luhan, N. Hemophilia presenting with intracranial hemorrhage. Am J Dis Child 1987; 141: 1215-1217.
-
(1987)
Am J Dis Child
, vol.141
, pp. 1215-1217
-
-
Bray, G.L.1
Luhan, N.2
-
30
-
-
0343820051
-
When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10 year single centre pup study
-
Pollman, H., Richter, H., Ringkamp, H., Jurgens, H. When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10 year single centre PUP study. Eur J Pediatr 1999; 158: S166-S170.
-
(1999)
Eur J Pediatr
, vol.158
, pp. S166-S170
-
-
Pollman, H.1
Richter, H.2
Ringkamp, H.3
Jurgens, H.4
-
31
-
-
0033373301
-
Prevalence and outcome of intracranial haemorrhage in haemophiliacs: A survey of the paediatric group of the german society of thrombosis and haemostasis (gth)
-
Klinge, J., Auberger, K., Auerswald, G., et al. Prevalence and outcome of intracranial haemorrhage in haemophiliacs: a survey of the paediatric group of the German Society of Thrombosis and Haemostasis (GTH). Eur J Pediatr 1999; 158: S162-S165.
-
(1999)
Eur J Pediatr
, vol.158
, pp. S162-S165
-
-
Klinge, J.1
Auberger, K.2
Auerswald, G.3
-
32
-
-
0033510285
-
Intracranial and extracranial hemorrhages in newborns with hemophilia: A review of the literature
-
Kulkarni, R., Lusher, J. M. Intracranial and extracranial hemorrhages in newborns with hemophilia: a review of the literature. J Pediatr Hematol Oncol 1999; 21:289-295.
-
(1999)
J Pediatr Hematol Oncol
, vol.21
, pp. 289-295
-
-
Kulkarni, R.1
Lusher, J.M.2
-
33
-
-
0006029896
-
Haemophilia a: Two cases showing unusual features at birth
-
Le Pommelet, C., Durand, P, Laurian, Y., Devictor, D. Haemophilia A: two cases showing unusual features at birth. Haemophilia 1998; 4:122-125.
-
(1998)
Haemophilia
, vol.4
, pp. 122-125
-
-
Le Pommelet, C.1
Durand, P.2
Laurian, Y.3
Devictor, D.4
-
34
-
-
0033019412
-
Splenic rupture in a newborn with hemophilia a: Case report and review of the literature
-
Johnson-Robbins, L. A., Porter, J. C., Horgan, M. J. Splenic rupture in a newborn with hemophilia A: case report and review of the literature. Clin Pediatr (Phila) 1999; 38: 117-119.
-
(1999)
Clin Pediatr (Phila)
, vol.38
, pp. 117-119
-
-
Johnson-Robbins, L.A.1
Porter, J.C.2
Horgan, M.J.3
-
35
-
-
0030828026
-
Hemophilia presenting in an infant as a radial artery pseudoaneurysm following arterial puncture
-
Fields, J. M., Saluja, S., Schwartz, D. S., Touloukian, R. J., Keller, M. S. Hemophilia presenting in an infant as a radial artery pseudoaneurysm following arterial puncture. Pediatr Radiol 1997;27: 763-764.
-
(1997)
Pediatr Radiol
, vol.27
, pp. 763-764
-
-
Fields, J.M.1
Saluja, S.2
Schwartz, D.S.3
Touloukian, R.J.4
Keller, M.S.5
-
37
-
-
0026686517
-
Circumcision in hemophilia: The use of fibrin glue for local hemostasis
-
Martinowitz, U., Varon, D., Jonas, R, et al. Circumcision in hemophilia: the use of fibrin glue for local hemostasis. J Urol 1992; 148: 855-857.
-
(1992)
J Urol
, vol.148
, pp. 855-857
-
-
Martinowitz, U.1
Varon, D.2
Jonas, R.3
-
39
-
-
0024636323
-
Hypercalcemia associated with normal i125-dihydroxyvitamin d concentrations in a neonate with factor ixdeficiency
-
Schwartz, I., Root, A. Hypercalcemia associated with normal I125-dihydroxyvitamin D concentrations in a neonate with factor IXdeficiency. J Pediatr 1989; 114: 509-510.
-
(1989)
J Pediatr
, vol.114
, pp. 509-510
-
-
Schwartz, I.1
Root, A.2
-
40
-
-
0024688389
-
Plasma support for surgery in a premature infant with factor ix deficiency
-
Pegelow, C. H., Borromeo, M. C., Daghastani, D., Band- stra, E. S. Plasma support for surgery in a premature infant with factor IX deficiency. Am J Dis Child 1989; 143: 639-640.
-
(1989)
Am J Dis Child
, vol.143
, pp. 639-640
-
-
Pegelow, C.H.1
Borromeo, M.C.2
Daghastani, D.3
Band- Stra, E.S.4
-
41
-
-
0024416133
-
Postdelivery headbleeding in hemophilic neonates: Causes and management
-
Kletzel, M., Miller, C. H., Becton, D. L., Chadduck, W. M., Elser, J. M. Postdelivery headbleeding in hemophilic neonates: causes and management. Am J Dis Child 1989; 143:1107-1110.
-
(1989)
Am J Dis Child
, vol.143
, pp. 1107-1110
-
-
Kletzel, M.1
Miller, C.H.2
Becton, D.L.3
Chadduck, W.M.4
Elser, J.M.5
-
42
-
-
0027508189
-
Haemophiliabliverpool: Anewbritishfamily with mild haemophilia b associated with a -6 g to a mutation in the factor ix promoter
-
Stowell, K., Figueiredo, M., Brownlee, G., Jones, P, Bolton- Maggs, P H. B. HaemophiliaBLiverpool: anewBritishfamily with mild haemophilia B associated with a -6 G to A mutation in the factor IX promoter. Br J Haematol 1993; 85: 188-190.
-
(1993)
Br J Haematol
, vol.85
, pp. 188-190
-
-
Stowell, K.1
Figueiredo, M.2
Brownlee, G.3
Jones, P.4
Bolton- Maggs, P.H.B.5
-
43
-
-
0006029765
-
Hemophilia and related hemorrhagic disorders
-
Hartmann, J., Diamond, L. Hemophilia and related hemorrhagic disorders. Practitioner 1957; 178:179-190.
-
(1957)
Practitioner
, vol.178
, pp. 179-190
-
-
Hartmann, J.1
Diamond, L.2
-
44
-
-
0025228548
-
Diagnostic symptoms of severe and moderate haemophilia a and b
-
Ljung, R., Petrini, P., Nilsson, I. Diagnostic symptoms of severe and moderate haemophilia A and B. Acta Paediatr Scand 1990; 79:196-200.
-
(1990)
Acta Paediatr Scand
, vol.79
, pp. 196-200
-
-
Ljung, R.1
Petrini, P.2
Nilsson, I.3
-
45
-
-
0014256510
-
Congenital fibrinogen deficiency
-
Manios, S., Schenck, W., Kunzer, W. Congenital fibrinogen deficiency. Acta Pediatr Scand 1968; 57: 145-180.
-
(1968)
Acta Pediatr Scand
, vol.57
, pp. 145-180
-
-
Manios, S.1
Schenck, W.2
Kunzer, W.3
-
46
-
-
0021738856
-
Transfusion support for congenital clotting deficiencies other than haemophilia
-
Lewis, J., Spero, J., Ragni, M., Bontempo, F. A. Transfusion support for congenital clotting deficiencies other than haemophilia. Clin Hematol 1984; 13: 119-135.
-
(1984)
Clin Hematol
, vol.13
, pp. 119-135
-
-
Lewis, J.1
Spero, J.2
Ragni, M.3
Bontempo, F.A.4
-
47
-
-
0019549277
-
Lesions hemorrag- iques intra-osseuses des afibrinemies congenitales: A propos d’un nouveau cas
-
Zenny, J., Chevrot, A., Sultan, Y., et al. Lesions hemorrag- iques intra-osseuses des afibrinemies congenitales: a propos d’un nouveau cas. J Radiol 1981:62:263-266.
-
(1981)
J Radiol
, vol.62
, pp. 263-266
-
-
Zenny, J.1
Chevrot, A.2
Sultan, Y.3
-
48
-
-
0018887670
-
Congenital afibrinogenemia in 10 offspring of uncle-niece marriages
-
Fried, K., Kaufman, S. Congenital afibrinogenemia in 10 offspring of uncle-niece marriages. Clin Genet 1980; 17: 223-227.
-
(1980)
Clin Genet
, vol.17
, pp. 223-227
-
-
Fried, K.1
Kaufman, S.2
-
49
-
-
0018142318
-
Severe congenital hypopro- thrombinemia
-
Gill, F., Shapiro, S., Schwartz, E. Severe congenital hypopro- thrombinemia. J Pediatr 1978; 93:264-266.
-
(1978)
J Pediatr
, vol.93
, pp. 264-266
-
-
Gill, F.1
Shapiro, S.2
Schwartz, E.3
-
50
-
-
0029402184
-
Intracranialhem-orrhage in congenital factor ii deficiency
-
Viola, L., Chiaretti, A., Lazzareschi, I., etal.Intracranialhem-orrhage in congenital factor II deficiency. Pediatr Med Chir 1995; 17: 593-594.
-
(1995)
Pediatr Med Chir
, vol.17
, pp. 593-594
-
-
Viola, L.1
Chiaretti, A.2
Lazzareschi, I.3
-
51
-
-
0015262553
-
Parahemophilia. Factor v deficiency
-
Seeler, R. Parahemophilia. Factor V deficiency. Med Clin NorthAm 1972; 56:119-125.
-
(1972)
Med Clin Northam
, vol.56
, pp. 119-125
-
-
Seeler, R.1
-
52
-
-
0023950622
-
Prenatal diagnosis and management of bleeding disorders with fetal blood sampling
-
Daffos, F., Forestier, F., Kaplan, C., Cox, W. Prenatal diagnosis and management of bleeding disorders with fetal blood sampling. AmJ Obstet Gynecol 1988; 158: 939-946.
-
(1988)
Amj Obstet Gynecol
, vol.158
, pp. 939-946
-
-
Daffos, F.1
Forestier, F.2
Kaplan, C.3
Cox, W.4
-
53
-
-
0033996029
-
Severe factorvdeficiencyand neonatal intracranial haemorrhage: A case report
-
Salooja, N., Martin, P., Khair, K., Liesner, R., Hann, I. Severe factorVdeficiencyand neonatal intracranial haemorrhage: a case report. Haemophilia 2000; 6: 44-46.
-
(2000)
Haemophilia
, vol.6
, pp. 44-46
-
-
Salooja, N.1
Martin, P.2
Khair, K.3
Liesner, R.4
Hann, I.5
-
54
-
-
0031797607
-
Severe factor v deficiency presenting as subdural haematoma in the newborn
-
Ehrenforth, S., Klarmann, D., Zabel, B., Scharrer, I., Kreuz, W. Severe factor V deficiency presenting as subdural haematoma in the newborn. Eur J Pediatr 1998; 157: 1032.
-
(1998)
Eur J Pediatr
, vol.157
, pp. 1032
-
-
Ehrenforth, S.1
Klarmann, D.2
Zabel, B.3
Scharrer, I.4
Kreuz, W.5
-
55
-
-
0030322654
-
Rare inherited coagulation disorders in india
-
Kashyap, R., Saxena, R., Choudhry, V P. Rare inherited coagulation disorders in India. Haematologia (Budap) 1996; 28: 13-19.
-
(1996)
Haematologia (Budap)
, vol.28
, pp. 13-19
-
-
Kashyap, R.1
Saxena, R.2
Choudhry, V.P.3
-
56
-
-
0021180472
-
Factor v deficiency and antenatal ventricular hemorrhage
-
Whitelaw, A., Haines, M., Bolsover, W., et al. Factor V deficiency and antenatal ventricular hemorrhage. Arch Dis Child 1984; 59:997-999.
-
(1984)
Arch Dis Child
, vol.59
, pp. 997-999
-
-
Whitelaw, A.1
Haines, M.2
Bolsover, W.3
-
57
-
-
0028249142
-
Congenital factorvdeficiencyandintraventricularhemorrhageof pre- natal origin
-
Bonvini, G., Cotta-Ramusino, A., Ricciardi, G. Congenital factorVdeficiencyandintraventricularhemorrhageof pre- natal origin. Pediatr Med Chir 1994; 16: 93-94.
-
(1994)
Pediatr Med Chir
, vol.16
, pp. 93-94
-
-
Bonvini, G.1
Cotta-Ramusino, A.2
Ricciardi, G.3
-
58
-
-
72849179156
-
Congenital deficiency of factor vii associated with hemorrhagic disease Of the newborn
-
Rabiner, S., Winick, M., Smith, C. Congenital deficiency of factor VII associated with hemorrhagic disease Of the newborn. Pediatrics 1960;25:101-105.
-
(1960)
Pediatrics
, vol.25
, pp. 101-105
-
-
Rabiner, S.1
Winick, M.2
Smith, C.3
-
59
-
-
0018395055
-
Intracranial hemorrhage in congenital factor vii deficiency
-
Matthay, K., Koerper, M., Ablin, A. R. Intracranial hemorrhage in congenital factor VII deficiency. J Pediatr 1979; 94: 413-415.
-
(1979)
J Pediatr
, vol.94
, pp. 413-415
-
-
Matthay, K.1
Koerper, M.2
Ablin, A.R.3
-
61
-
-
0019465270
-
Spero, j., etal. factorvii deficiency
-
Ragni, M., Lewis, J., Spero, J., etal. FactorVII deficiency. Am J Hematol 1981;10: 79-88.
-
(1981)
Am J Hematol
, vol.10
, pp. 79-88
-
-
Ragni, M.1
Lewis, J.2
-
62
-
-
0014858462
-
Dubin-johnston syndrome in israel: Association with factor vii deficiency
-
Seligsohn, U., Shani, M., Ramot, B. Dubin-Johnston syndrome in Israel: association with factor VII deficiency. Q J Med 1970; 39: 569-584.
-
(1970)
Q J Med
, vol.39
, pp. 569-584
-
-
Seligsohn, U.1
Shani, M.2
Ramot, B.3
-
63
-
-
0031711654
-
Development of a subdural vein thrombosis following aggressive factor vii replacement for postnatalintracranialhaemorrhageinahomozygousfactor vii-deficient infant
-
Worth, L. L., Hoots, W. K. Development of a subdural vein thrombosis following aggressive factor VII replacement for postnatalintracranialhaemorrhageinahomozygousfactor VII-deficient infant. Haemophilia 1998;4:757-761.
-
(1998)
Haemophilia
, vol.4
, pp. 757-761
-
-
Worth, L.L.1
Hoots, W.K.2
-
64
-
-
0034005045
-
Clinical efficacy and recovery levels of recombinant fviia (novoseven) in the treatment of intracranial haemorrhage in severe neonatal fvii deficiency
-
Wong, W. Y., Huang, W. C., Miller, R., McGinty, K., Whisnant, J. K. Clinical efficacy and recovery levels of recombinant FVIIa (NovoSeven) in the treatment of intracranial haemorrhage in severe neonatal FVII deficiency. Haemophilia 2000; 6: 50-54.
-
(2000)
Haemophilia
, vol.6
, pp. 50-54
-
-
Wong, W.Y.1
Huang, W.C.2
Miller, R.3
McGinty, K.4
Whisnant, J.K.5
-
65
-
-
0024336513
-
Relationship between human development and disappearance of unusually large von willebrand factor multimers from plasma
-
Katz, J. A., Moake, J. L., McPherson, P D., et al. Relationship between human development and disappearance of unusually large von Willebrand factor multimers from plasma. Blood 1989; 73:1851-1858.
-
(1989)
Blood
, vol.73
, pp. 1851-1858
-
-
Katz, J.A.1
Moake, J.L.2
McPherson, P.D.3
-
66
-
-
0024591755
-
Fetal and neonatal von willebrand factor (vwf) is unusually large and similar to the vwf in patients with thrombotic thrombocytopenic purpura
-
Weinstein, M. J., Blanchard, R., Moake, J. L., Vosburgh, E., Moise, K. Fetal and neonatal von Willebrand factor (vWF) is unusually large and similar to the vWF in patients with thrombotic thrombocytopenic purpura. Br J Haematol 1989; 72: 68-72.
-
(1989)
Br J Haematol
, vol.72
, pp. 68-72
-
-
Weinstein, M.J.1
Blanchard, R.2
Moake, J.L.3
Vosburgh, E.4
Moise, K.5
-
67
-
-
0023181385
-
Type iib vonwille- brand’s disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy
-
Donner, M., Holmberg, L., Nilsson, I. M. Type IIB vonWille- brand’s disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy. Br J Haematol 1987; 66: 349-354.
-
(1987)
Br J Haematol
, vol.66
, pp. 349-354
-
-
Donner, M.1
Holmberg, L.2
Nilsson, I.M.3
-
68
-
-
0025080041
-
Rapid neonatal diagnosis of von willebrand’s disease by use of the polymerase chain reaction
-
Bignall, P., Standen, G., Bowen, D. J., Peake, I., Bloom, A. L. Rapid neonatal diagnosis of von Willebrand’s disease by use of the polymerase chain reaction. Lancet 1990; 336:638-639.
-
(1990)
Lancet
, vol.336
, pp. 638-639
-
-
Bignall, P.1
Standen, G.2
Bowen, D.J.3
Peake, I.4
Bloom, A.L.5
-
69
-
-
0023813748
-
Treatment of type iii von willebrand’s disease with solvent/detergent- treated factor viii concentrates
-
Gazengel, C., Fischer, A., Schlegel, N., et al. Treatment of type III von Willebrand’s disease with solvent/detergent- treated factor VIII concentrates. Nouv Rev Fr Hematol 1988; 30: 225-227.
-
(1988)
Nouv Rev Fr Hematol
, vol.30
, pp. 225-227
-
-
Gazengel, C.1
Fischer, A.2
Schlegel, N.3
-
70
-
-
0023091143
-
Assessment of multimeric structure and ristocetin-induced binding to platelets of von willebrand factor present in cry- oprecipitateanddifferentfactorviii concentrates
-
Lopez-Fernandez, M. F., Lopez-Berges, C., Corral, M., etal. Assessment of multimeric structure and ristocetin-induced binding to platelets of von Willebrand factor present in cry- oprecipitateanddifferentfactorVIII concentrates. Vox Sang 1987; 52:15-19.
-
(1987)
Vox Sang
, vol.52
, pp. 15-19
-
-
Lopez-Fernandez, M.F.1
Lopez-Berges, C.2
Corral, M.3
-
71
-
-
0018938377
-
Factorxdefi-ciency in the neonatal period
-
Machin, S., Winter, M., Davies, S., Mackie, I. FactorXdefi-ciency in the neonatal period. Arch Dis Child 1980; 55: 406-408.
-
(1980)
Arch Dis Child
, vol.55
, pp. 406-408
-
-
Machin, S.1
Winter, M.2
Davies, S.3
Mackie, I.4
-
72
-
-
0026551222
-
Prevention of recurrent intracranial hemorrhage in a factor x deficient infant
-
Sandler, E., Gross, S. Prevention of recurrent intracranial hemorrhage in a factor X deficient infant. Am J Pediatr Hematol Oncol 1992; 14:163-165.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 163-165
-
-
Sandler, E.1
Gross, S.2
-
73
-
-
0025641032
-
Factor x deficiency: A rare cause of scrotalhaemorrhage
-
Ruane, B., McCord, F. Factor X deficiency: a rare cause of scrotalhaemorrhage. Irish Med J 1990; 83:163.
-
(1990)
Irish Med J
, vol.83
, pp. 163
-
-
Ruane, B.1
McCord, F.2
-
74
-
-
0025838274
-
Neonatal congenital factorxdefi- ciency
-
El Kalla, S., Menon, N. S. Neonatal congenital FactorXdefi- ciency. Pediatr Hematol Oncol 1991; 8: 347-354.
-
(1991)
Pediatr Hematol Oncol
, vol.8
, pp. 347-354
-
-
El Kalla, S.1
Menon, N.S.2
-
75
-
-
0023719416
-
Antenatally diagnosed subdural haemorrhage in congenital factor x deficiency
-
De Sousa, C., Clark, T., Bradshaw, A. Antenatally diagnosed subdural haemorrhage in congenital factor X deficiency. Arch Dis Child 1988; 63:1168-1174.
-
(1988)
Arch Dis Child
, vol.63
, pp. 1168-1174
-
-
de Sousa, C.1
Clark, T.2
Bradshaw, A.3
-
76
-
-
0014223265
-
The enigma of severe factor xi deficiency without hemorrhagic symptoms: Distinction from hageman factor and “fletcher factor” deficiency; family study; and problems of diagnosis
-
Edson, J. R., White, J. G., Krivit, W. The enigma of severe factor XI deficiency without hemorrhagic symptoms: distinction from Hageman factor and “Fletcher factor” deficiency; family study; and problems of diagnosis. Thromb Diath Haemorrh 1967; 18: 342-348.
-
(1967)
Thromb Diath Haemorrh
, vol.18
, pp. 342-348
-
-
Edson, J.R.1
White, J.G.2
Krivit, W.3
-
77
-
-
0025817821
-
Factorxi: Areviewofitsbiochemistryand deficiency
-
Kitchens, C. FactorXI:areviewofitsbiochemistryand deficiency. Semin Thromb Haemost 1991; 17:55-72.
-
(1991)
Semin Thromb Haemost
, vol.17
, pp. 55-72
-
-
Kitchens, C.1
-
78
-
-
0031837035
-
Fetal bilateral subdural haemorrhages: Prenatal diagnosis and spontaneous resolutionbytime of delivery
-
Barozzino, T., Sgro, M., Toi, A., et al. Fetal bilateral subdural haemorrhages: prenatal diagnosis and spontaneous resolutionbytime of delivery. Prenat Diagn 1998; 18:496-503.
-
(1998)
Prenat Diagn
, vol.18
, pp. 496-503
-
-
Barozzino, T.1
Sgro, M.2
Toi, A.3
-
79
-
-
33947268119
-
Hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency
-
Duckert, F., Jung, E., Shmerling, D. Hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency.Thromb Diath Haemorrh 1960; 5: 179.
-
(1960)
Thromb Diath Haemorrh
, vol.5
, pp. 179
-
-
Duckert, F.1
Jung, E.2
Shmerling, D.3
-
80
-
-
0342412065
-
Congenital deficiency of fibrin stabilizing factor: Observation of a new case
-
Barry, A., Delage, M. Congenital deficiency of fibrin stabilizing factor: observation of a new case. N Engl J Med 1965; 272: 943-946.
-
(1965)
N Engl J Med
, vol.272
, pp. 943-946
-
-
Barry, A.1
Delage, M.2
-
81
-
-
0013932934
-
Factor 13 deficiency with severe hemorrhage diathesis
-
Fisher, S., Rikover, M., Naor, S. Factor 13 deficiency with severe hemorrhage diathesis. Blood 1966; 28:34-9.
-
(1966)
Blood
, vol.28
, pp. 34-39
-
-
Fisher, S.1
Rikover, M.2
Naor, S.3
-
82
-
-
0014147852
-
Congenital deficiency of factor 13 (fibrin- stabilizing factor): Report of a case and review of the literature
-
Britten, A. F. H. Congenital deficiency of factor 13 (fibrin- stabilizing factor): report of a case and review of the literature. Am J Med 1967; 43: 751-761.
-
(1967)
Am J Med
, vol.43
, pp. 751-761
-
-
Britten, A.F.H.1
-
83
-
-
0015175129
-
Congenital factor xiii deficiency: Observationoftwocasesinthe newbornperiod
-
Ozsoylu, S., Altay, C., Hi csonmez, G. Congenital factor XIII deficiency: Observationoftwocasesinthe newbornperiod. Am JDis Child 1971;122: 541-543.
-
(1971)
Am Jdis Child
, vol.122
, pp. 541-543
-
-
Ozsoylu, S.1
Altay, C.2
Hi Csonmez, G.3
-
84
-
-
0018127222
-
Congenital factor xiii deficiency in a neonate
-
Francis, J., Todd, P. Congenital factor XIII deficiency in a neonate. Br Med J 1978;2:1532.
-
(1978)
Br Med J
, vol.2
, pp. 1532
-
-
Francis, J.1
Todd, P.2
-
85
-
-
0026892687
-
Congenital factor xiii deficiency
-
Merchant, R., Agarwal, B. R., Currimbhoy, Z., Pherwani, A., Avasthi, B. Congenital factor XIII deficiency. Ind Pediatr 1992; 29:831-836.
-
(1992)
Ind Pediatr
, vol.29
, pp. 831-836
-
-
Merchant, R.1
Agarwal, B.R.2
Currimbhoy, Z.3
Pherwani, A.4
Avasthi, B.5
-
86
-
-
0030817494
-
Late hemorrhagic disease of the newborn as a cause of intracerebral bleeding
-
Solves, P., Altes, A., Ginovart, G., Demestre, J., Fontcu- berta, J. Late hemorrhagic disease of the newborn as a cause of intracerebral bleeding. Ann Hematol 1997; 75:65-66.
-
(1997)
Ann Hematol
, vol.75
, pp. 65-66
-
-
Solves, P.1
Altes, A.2
Ginovart, G.3
Demestre, J.4
Fontcu- Berta, J.5
-
87
-
-
8044259620
-
Etro working party on factorxiii questionnaire oncongenital factorxiii deficiency in europe: Status and perspectives
-
Seitz, R., Duckert, F., Lopaciuk, S., etal. ETRO Working Party on FactorXIII questionnaire oncongenital factorXIII deficiency in Europe: status and perspectives. Semin Thromb Hemost 1996; 22: 415-418.
-
(1996)
Semin Thromb Hemost
, vol.22
, pp. 415-418
-
-
Seitz, R.1
Duckert, F.2
Lopaciuk, S.3
-
88
-
-
0027265085
-
Congenitaldeficiencyoffibrinstabilizingfac-tor (factorxiii)
-
Blanckaert, D., Oueidat, I., Chelala, J., Loeuille, G. A., Delepoulle, F.Congenitaldeficiencyoffibrinstabilizingfac-tor (factorXIII). Pediatrie 1993; 48: 451-453.
-
(1993)
Pediatrie
, vol.48
, pp. 451-453
-
-
Blanckaert, D.1
Oueidat, I.2
Chelala, J.3
Loeuille, G.A.4
Delepoulle, F.5
-
89
-
-
0023926397
-
Clinical experience with a pasteurised human plasma concentrate in factor xiii deficiency
-
Daly, H. M., Haddon, M. E. Clinical experience with a pasteurised human plasma concentrate in factor XIII deficiency. Thromb Haemost 1988; 59:171-174.
-
(1988)
Thromb Haemost
, vol.59
, pp. 171-174
-
-
Daly, H.M.1
Haddon, M.E.2
-
90
-
-
0021876026
-
Neonatal factor xiii deficiency
-
Landman, J., Creter, D., Homburg, R., Sirota, L., Dulitzky, F. Neonatal factor XIII deficiency. Clin Pediatr (Phila) 1985; 24: 352-353.
-
(1985)
Clin Pediatr (Phila)
, vol.24
, pp. 352-353
-
-
Landman, J.1
Creter, D.2
Homburg, R.3
Sirota, L.4
Dulitzky, F.5
-
91
-
-
0015498627
-
Documentation of the plasma factor xiii defi- ciencyinman
-
Duckert, F. Documentation of the plasma factor XIII defi- ciencyinman. Ann NYA cad Sci 1972; 202:190-199.
-
(1972)
Ann NYA Cad Sci
, vol.202
, pp. 190-199
-
-
Duckert, F.1
-
92
-
-
0031743817
-
Factor concentrates for the treatment of factorxiii deficiency
-
Gootenberg, J. E. Factor concentrates for the treatment of factorXIII deficiency. Curr Opin Hematol 1998; 5:372-375.
-
(1998)
Curr Opin Hematol
, vol.5
, pp. 372-375
-
-
Gootenberg, J.E.1
-
93
-
-
85040263171
-
Combined congenital clotting factor abnormalities
-
Mammen, E., Murano, G., Bick, R. L. Combined congenital clotting factor abnormalities.Semin Thromb Haemost 1983; 9: 55-56.
-
(1983)
Semin Thromb Haemost
, vol.9
, pp. 55-56
-
-
Mammen, E.1
Murano, G.2
Bick, R.L.3
-
94
-
-
0026548386
-
Coagulation-factor deficiencies and abnormal bleeding in noonan’s syndrome
-
Sharland, M., Patton, M. A., Talbot, S., Chitolie, A., Bevan, D. H. Coagulation-factor deficiencies and abnormal bleeding in Noonan’s syndrome. Lancet 1992; 339:19-21.
-
(1992)
Lancet
, vol.339
, pp. 19-21
-
-
Sharland, M.1
Patton, M.A.2
Talbot, S.3
Chitolie, A.4
Bevan, D.H.5
-
95
-
-
0020036782
-
Congenital deficiency of alpha-2-plasmin inhibitor in three sisters
-
Yoshioka, A., Kamitsuji, H., Takase, T., et al. Congenital deficiency of alpha-2-plasmin inhibitor in three sisters. Haemostasis 1982; 11:176-184.
-
(1982)
Haemostasis
, vol.11
, pp. 176-184
-
-
Yoshioka, A.1
Kamitsuji, H.2
Takase, T.3
-
96
-
-
0023857728
-
Mild haemostatic problems associatedwith congenital heterozygous alpha2- antiplasmin deficiency
-
Leebeek, F. W., Stibbe, J., Knot, E. A., et al. Mild haemostatic problems associatedwith congenital heterozygous alpha2- antiplasmin deficiency. Thromb Haemost 1988; 59:96-100.
-
(1988)
Thromb Haemost
, vol.59
, pp. 96-100
-
-
Leebeek, F.W.1
Stibbe, J.2
Knot, E.A.3
-
97
-
-
0022378738
-
Severe hemorrhagic tendencyinheterozygousalpha-2-antiplasmin deficiency
-
Kordich, L., Feldman, L., Porterie, P, Lago, O. Severe hemorrhagic tendencyinheterozygousalpha-2-antiplasmin deficiency. Thromb Res 1985:40:645-651.
-
(1985)
Thromb Res
, vol.40
, pp. 645-651
-
-
Kordich, L.1
Feldman, L.2
Porterie, P.3
Lago, O.4
-
98
-
-
0021991991
-
Ableeding disorder due to deficiency of alpha-2-antiplasmin
-
Kettle, P, Mayne, E. E.Ableeding disorder due to deficiency of alpha-2-antiplasmin. J Clin Pathol 1985; 38: 428-429.
-
(1985)
J Clin Pathol
, vol.38
, pp. 428-429
-
-
Kettle, P.1
Mayne, E.E.2
-
99
-
-
0019985539
-
Ableeding disorder due to deficiencyof alpha- 2-antiplasmin
-
Miles, L. A., Plow, E. F., Donnelly, K. J., Hougie, C., Griffin, J. H.Ableeding disorder due to deficiencyof alpha- 2-antiplasmin. Blood 1982; 59:1246-1251.
-
(1982)
Blood
, vol.59
, pp. 1246-1251
-
-
Miles, L.A.1
Plow, E.F.2
Donnelly, K.J.3
Hougie, C.4
Griffin, J.H.5
-
100
-
-
0019989383
-
Familial hemorrhagic diathesis in a dutch family: An inherited deficiency of alpha-2-antiplasmin
-
Kluft, C., Vellenga, A., Brommer, E. J. P., Wijngaards, G. A familial hemorrhagic diathesis in a Dutch family: an inherited deficiency of alpha-2-antiplasmin. Blood 1982; 59:1169-1180.
-
(1982)
Blood
, vol.59
, pp. 1169-1180
-
-
Kluft, C.1
Vellenga, A.2
Brommer, E.J.P.3
Wijngaards, G.A.4
-
101
-
-
0031788597
-
A case of intramedullary haematoma associated with congenital alpha2-plasmin inhibitor deficiency
-
Devaussuzenet, V. M. P., Ducou-le-Pointe, H. A., Doco, A. M., et al. A case of intramedullary haematoma associated with congenital alpha2-plasmin inhibitor deficiency. Pediatr Radiol 1998; 28: 978-980.
-
(1998)
Pediatr Radiol
, vol.28
, pp. 978-980
-
-
Devaussuzenet, V.M.P.1
Ducou-Le-pointe, H.A.2
Doco, A.M.3
-
102
-
-
0022994822
-
Epsilon-aminocaproicacidinthetreatmentof patients with acute promyelocytic leukemia and acquired alpha- 2-plasmin inhibitor deficiency
-
Schwartz, B. S., Williams, E. C., Conlan, M. G., Mosher, D.F.Epsilon-aminocaproicacidinthetreatmentof patients with acute promyelocytic leukemia and acquired alpha- 2-plasmin inhibitor deficiency. Ann Intern Med 1986; 105: 873-877.
-
(1986)
Ann Intern Med
, vol.105
, pp. 873-877
-
-
Schwartz, B.S.1
Williams, E.C.2
Conlan, M.G.3
Mosher, D.F.4
-
103
-
-
0033654989
-
Homozygous quantitative defect of alpha 2-antiplasmin in a family from central slovakia
-
Zarnovicanova, M., Mocikova, K. A homozygous quantitative defect of alpha 2-antiplasmin in a family from central Slovakia. Bratisl Lek Listy 2000; 101: 28-30.
-
(2000)
Bratisl Lek Listy
, vol.101
, pp. 28-30
-
-
Zarnovicanova, M.1
Mocikova, K.A.2
-
104
-
-
0023766960
-
Placental transfer of vitamin k1 and its implications in fetal haemostasis
-
Mandelbrot, L., Guillaumont, M., Forestier, F., et al. Placental transfer of vitamin K1 and its implications in fetal haemostasis. Thromb Haemost 1988; 60: 39-43.
-
(1988)
Thromb Haemost
, vol.60
, pp. 39-43
-
-
Mandelbrot, L.1
Guillaumont, M.2
Forestier, F.3
-
105
-
-
0019997972
-
Plasma vitamin k1 in mothers and their newborn babies
-
Shearer, M. J., Barkhan, P, Rahim, S., Stimmler, L. Plasma vitamin K1 in mothers and their newborn babies. Lancet 1982; 2: 460-463.
-
(1982)
Lancet
, vol.2
, pp. 460-463
-
-
Shearer, M.J.1
Barkhan, P.2
Rahim, S.3
Stimmler, L.4
-
106
-
-
0023819105
-
Vitamin k1 (phylloquinone) and vitamin k2 (menaquinone) status in newborns during the first week of life
-
Greer, F. R., Mummah-Schendel, L. L., Marshall, S., Suttie, J. W. Vitamin K1 (phylloquinone) and vitamin K2 (menaquinone) status in newborns during the first week of life. Pediatrics 1988; 81:137-140.
-
(1988)
Pediatrics
, vol.81
, pp. 137-140
-
-
Greer, F.R.1
Mummah-Schendel, L.L.2
Marshall, S.3
Suttie, J.W.4
-
107
-
-
0023722762
-
Determination of k vitamins (phylloquinone and menaquinones) in umbilical cord plasma by a platinum-reduction column
-
Hiraike, H., Kimura, M., Itokawa, Y. Determination of K vitamins (phylloquinone and menaquinones) in umbilical cord plasma by a platinum-reduction column. J Chromotogr 1988; 430:143-148.
-
(1988)
J Chromotogr
, vol.430
, pp. 143-148
-
-
Hiraike, H.1
Kimura, M.2
Itokawa, Y.3
-
108
-
-
45449121910
-
Distribution of k vitamins (phylloquinone and menaquinones) in human placenta and maternal and umbilical cord plasma
-
Hiraike, H., Kimura, M., Itokawa, Y. Distribution of K vitamins (phylloquinone and menaquinones) in human placenta and maternal and umbilical cord plasma. Am J Obstet Gynecol 1988; 158: 564-569.
-
(1988)
Am J Obstet Gynecol
, vol.158
, pp. 564-569
-
-
Hiraike, H.1
Kimura, M.2
Itokawa, Y.3
-
109
-
-
0020055382
-
Maternal anticonvulsant therapy and hemorrhagic disease of the newborn
-
Srinivasan, G., Seeler, R. A., Tiruvury, A., Pildes, R. S. Maternal anticonvulsant therapy and hemorrhagic disease of the newborn. Obstet Gynecol 1982; 59: 250-252.
-
(1982)
Obstet Gynecol
, vol.59
, pp. 250-252
-
-
Srinivasan, G.1
Seeler, R.A.2
Tiruvury, A.3
Pildes, R.S.4
-
110
-
-
0014935549
-
Neonatal coagulation defect due to anticonvulsant drug treatment in pregnancy
-
Mountain, K. R., Hirsh, J., Gallius, A. S. Neonatal coagulation defect due to anticonvulsant drug treatment in pregnancy. Lancet 1970; 1: 265-268.
-
(1970)
Lancet
, vol.1
, pp. 265-268
-
-
Mountain, K.R.1
Hirsh, J.2
Gallius, A.S.3
-
111
-
-
0024235076
-
Hemorrhagic disease of the newborn after maternal anticonvulsant therapy: A case report and literature review
-
Laosombat, V. Hemorrhagic disease of the newborn after maternal anticonvulsant therapy: a case report and literature review. J Med Assoc Thailand 1988; 71:643-648.
-
(1988)
J Med Assoc Thailand
, vol.71
, pp. 643-648
-
-
Laosombat, V.1
-
112
-
-
0017178395
-
Haemorrhagic disease of the newborn in the offspring of rifampicin and isoniazid treated mothers
-
Eggermont, E., Logghe, N., Van De Casseye, W., et al. Haemorrhagic disease of the newborn in the offspring of rifampicin and isoniazid treated mothers. Acta Paediatr Belg 1976; 29:87-90.
-
(1976)
Acta Paediatr Belg
, vol.29
, pp. 87-90
-
-
Eggermont, E.1
Logghe, N.2
Van De Casseye, W.3
-
113
-
-
0033016161
-
Deficiency bleeding (vkdb) in infancy. Isth pediatric/perinatal subcommittee. international society on thrombosis and haemostasis
-
Sutor, A. H., Von Kries, R., Cornelissen, E. A., McNinch, A. W., Andrew, M. Vitamin K deficiency bleeding (VKDB) in infancy. ISTH Pediatric/Perinatal Subcommittee. International Society on Thrombosis and Haemostasis. Thromb Haemost 1999; 81: 456-461.
-
(1999)
Thromb Haemost
, vol.81
, pp. 456-461
-
-
Sutor, A.H.1
Von Kries, R.2
Cornelissen, E.A.3
McNinch, A.W.4
Andrew, M.5
Vitamin, K.6
-
114
-
-
0022647468
-
Influence of the type of feedingonthepresence of pivka-ii in infants
-
Widdershoven, J., Motohara, K., Endo, F., Matsuda, I., Monnens, L. Influence of the type of feedingonthepresence of PIVKA-II in infants. Helv Paediatr Acta 1986; 41:25-29.
-
(1986)
Helv Paediatr Acta
, vol.41
, pp. 25-29
-
-
Widdershoven, J.1
Motohara, K.2
Endo, F.3
Matsuda, I.4
Monnens, L.5
-
115
-
-
0022139499
-
Editorial. Late onset of hemorrhagic disease of the newborn
-
Editorial. Late onset of hemorrhagic disease of the newborn. Nutr Rev 1985; 43: 303.
-
(1985)
Nutr Rev
, vol.43
, pp. 303
-
-
-
116
-
-
0024584614
-
Late neonatal vitamin k deficiency associated with subclinical liver dysfunction in human milk fed infants
-
Matsuda, I., Nishiyama, S., Motohara, K., etal. Late neonatal vitamin K deficiency associated with subclinical liver dysfunction in human milk fed infants. J Pediatr 1989; 114: 602-605.
-
(1989)
J Pediatr
, vol.114
, pp. 602-605
-
-
Matsuda, I.1
Nishiyama, S.2
Motohara, K.3
-
117
-
-
0023857784
-
Vitamin k-dependent clotting factors during longterm parenteral nutrition in full- term and preterm infants
-
Goldschmidt, B., Bors, S., Szabo, A. Vitamin K-dependent clotting factors during longterm parenteral nutrition in full- term and preterm infants. J Pediatr 1988;112:108-111.
-
(1988)
J Pediatr
, vol.112
, pp. 108-111
-
-
Goldschmidt, B.1
Bors, S.2
Szabo, A.3
-
118
-
-
0023320455
-
Screening for late neonatal vitamin k deficiency by acarboxyprothrombin in dried blood spots
-
Motohara, K., Endo, F., Matsuda, I. Screening for late neonatal vitamin K deficiency by acarboxyprothrombin in dried blood spots. Arch Dis Child 1987; 62: 370-375.
-
(1987)
Arch Dis Child
, vol.62
, pp. 370-375
-
-
Motohara, K.1
Endo, F.2
Matsuda, I.3
-
119
-
-
0020514266
-
Delayed presentation of haemorrhagic disease of the newborn
-
Forbes, D. Delayed presentation of haemorrhagic disease of the newborn. Med JAust 1983; 2:136-138.
-
(1983)
Med Jaust
, vol.2
, pp. 136-138
-
-
Forbes, D.1
-
120
-
-
0021346008
-
Vitamin k deficiency in newborns: A case report in a-1-antitrypsin deficiency and a review of factors predisposing to hemorrhage
-
Payne, N. R., Hasegawa, D. K. Vitamin K deficiency in newborns: a case report in a-1-antitrypsin deficiency and a review of factors predisposing to hemorrhage. Pediatrics 1984; 73:712-716.
-
(1984)
Pediatrics
, vol.73
, pp. 712-716
-
-
Payne, N.R.1
Hasegawa, D.K.2
-
121
-
-
0021721606
-
Intracranial hemorrhage and vitamin k deficiency in early infancy
-
Chaou, W.-T., Chou, M.-L., Eitzman, D. V. Intracranial hemorrhage and vitamin K deficiency in early infancy. J Pediatr 1984; 105:880-884.
-
(1984)
J Pediatr
, vol.105
, pp. 880-884
-
-
Chaou, W.-T.1
Chou, M.-L.2
Eitzman, D.V.3
-
122
-
-
0018860328
-
Factor ii antigen in liver disease and warfarin-induced vitamin k deficiency: Correlation with coagulation activity using echis venom
-
Corrigan, J. J., Jr, Earnest, D. Factor II antigen in liver disease and warfarin-induced vitamin K deficiency: correlation with coagulation activity using Echis venom. Am JHaematol 1980; 8: 249-255.
-
(1980)
Am Jhaematol
, vol.8
, pp. 249-255
-
-
Corrigan, J.J.1
Earnest, D.2
-
123
-
-
0020701727
-
Epidemic of haem- orrhagic disease invietnamese infants caused bywarfarin- contaminated talcs
-
Martin-Bouyer, G., Linh, P. D., Tuan, L. C. Epidemic of haem- orrhagic disease inVietnamese infants caused bywarfarin- contaminated talcs. Lancet 1983; 1:230-233.
-
(1983)
Lancet
, vol.1
, pp. 230-233
-
-
Martin-Bouyer, G.1
Linh, P.D.2
Tuan, L.C.3
-
124
-
-
0021964966
-
Detection of vitamin k deficiency by use of an enzyme- linked immunosorbent assayfor circulating abnormal prothrombin
-
Motohara, K., Kuroki, Y., Kan, H., Endo, F., Matsuda, I. Detection of vitamin K deficiency by use of an enzyme- linked immunosorbent assayfor circulating abnormal prothrombin. PediatrRes 1985;19: 354-357.
-
(1985)
Pediatrres
, vol.19
, pp. 354-357
-
-
Motohara, K.1
Kuroki, Y.2
Kan, H.3
Endo, F.4
Matsuda, I.5
-
125
-
-
0001223970
-
Observation on the prophylactic use of vitamin k in the newborn
-
Vietti, T. J., Murphy, T. P, James, J. A., Pritchard, J. A. Observation on the prophylactic use of vitamin K in the newborn. J Pediatr 1960; 56: 343-346.
-
(1960)
J Pediatr
, vol.56
, pp. 343-346
-
-
Vietti, T.J.1
Murphy, T.P.2
James, J.A.3
Pritchard, J.A.4
-
126
-
-
0014088509
-
Hemorrhagic disease of the newborn: Breast feeding as a necessaryfactor in the pathogenesis
-
Sutherland, J. M., Glueck, H. I. Hemorrhagic disease of the newborn: breast feeding as a necessaryfactor in the pathogenesis. Am J Dis Child 1967; 113: 524-533.
-
(1967)
Am J Dis Child
, vol.113
, pp. 524-533
-
-
Sutherland, J.M.1
Glueck, H.I.2
-
127
-
-
73049125025
-
Vitamin k-1 prophylaxis inthe newborn
-
Vietti, T. J., Stephens, J. C., Bennett, K. R. Vitamin K-1 prophylaxis inthe newborn. J Am Med Assoc 1961;176:791.
-
(1961)
J am Med Assoc
, vol.176
, pp. 791
-
-
Vietti, T.J.1
Stephens, J.C.2
Bennett, K.R.3
-
128
-
-
0023697608
-
Plasma concentrations of vitamin k1 and pivka-ii inbottle-fed and breast-fed infants with and without vitamin k prophylaxis atbirth
-
Widdershoven, J., Lambert, W., Motohara, K., etal. Plasma concentrations of vitamin K1 and PIVKA-II inbottle-fed and breast-fed infants with and without vitamin K prophylaxis atbirth. Eur J Pediatr 1988; 148:139-142.
-
(1988)
Eur J Pediatr
, vol.148
, pp. 139-142
-
-
Widdershoven, J.1
Lambert, W.2
Motohara, K.3
-
129
-
-
0023913293
-
Vitamin k effect in low birth weight infants
-
Ogata, T., Motohara, K., Endo, F., et al. Vitamin K effect in low birth weight infants. Pediatrics 1988; 81: 423-427.
-
(1988)
Pediatrics
, vol.81
, pp. 423-427
-
-
Ogata, T.1
Motohara, K.2
Endo, F.3
-
130
-
-
0023610403
-
Acarboxyprothrombin activity after oral prophylactic vitamin k
-
Von Kries, R., Kreppel, S., Becker, A., Gobel, U., Tanger-mann, R. Acarboxyprothrombin activity after oral prophylactic vitamin K. ArchDis Child 1987; 62:938-940.
-
(1987)
Archdis Child
, vol.62
, pp. 938-940
-
-
Von Kries, R.1
Kreppel, S.2
Becker, A.3
Gobel, U.4
Tanger-Mann, R.5
-
131
-
-
0013495982
-
The role of vitamin k in the etiology, prevention, and treatment of hemorrhage in the newborn infant: Part ii
-
Waddell, W. W., Guerry, D. The role of vitamin K in the etiology, prevention, and treatment of hemorrhage in the newborn infant: part II. JPediatr 1939; 15:802.
-
(1939)
Jpediatr
, vol.15
, pp. 802
-
-
Waddell, W.W.1
Guerry, D.2
-
132
-
-
0023924941
-
The second nationwide survey in japan of vitamin k deficiency in infants
-
Hanawa, Y., Maki, M., Murata, B., etal. The second nationwide survey in Japan of vitamin K deficiency in infants. Eur JPediatr 1988; 147: 472-477.
-
(1988)
Eur Jpediatr
, vol.147
, pp. 472-477
-
-
Hanawa, Y.1
Maki, M.2
Murata, B.3
-
133
-
-
0026695340
-
Child-hood cancer, intramuscular vitamin k, and pethidine given during labour
-
Golding, J., Greenwood, R., Birmingham, K., Mott, M.Child-hood cancer, intramuscular vitamin K, and pethidine given during labour. Br Med J 1992; 305: 341-346.
-
(1992)
Br Med J
, vol.305
, pp. 341-346
-
-
Golding, J.1
Greenwood, R.2
Birmingham, K.3
Mott, M.4
-
134
-
-
0026707635
-
Vitamin k prophylaxis and vitamin kdeficiencybleeding (vkdb) in earlyinfancy
-
Von Kries, R., Gobel, U. Vitamin K prophylaxis and vitamin Kdeficiencybleeding (VKDB) in earlyinfancy ActaPaediatr 1992;81:655-657.
-
(1992)
Actapaediatr
, vol.81
, pp. 655-657
-
-
Von Kries, R.1
Gobel, U.2
-
135
-
-
0023811930
-
Neonatal vitamin k prophylaxis and vitamin k deficiency hemorrhages in switzerland 1986-1988
-
Tonz, O., Schubiger, G. Neonatal vitamin K prophylaxis and vitamin K deficiency hemorrhages in Switzerland 1986-1988. Schweiz Med Wochenschr 1988; 118: 1747-1752.
-
(1988)
Schweiz Med Wochenschr
, vol.118
, pp. 1747-1752
-
-
Tonz, O.1
Schubiger, G.2
-
136
-
-
0027156826
-
Evaluation of a daily dose of 25 g vitamin k1 to prevent vitamin k deficiency in breast-fed infants
-
Cornelissen, E. A. M., Kollee, L. A. A., van Lith, T. G. P. J., Motohara, K., Monnens, L. A. H. Evaluation of a daily dose of 25 g Vitamin K1 to prevent vitamin K deficiency in breast-fed infants. J Pediatr Gastroenterol Nutr 1993; 16: 301-305.
-
(1993)
J Pediatr Gastroenterol Nutr
, vol.16
, pp. 301-305
-
-
Cornelissen, E.A.M.1
Kollee, L.A.A.2
Van Lith, T.G.P.J.3
Motohara, K.4
Monnens, L.A.H.5
-
137
-
-
0031014670
-
Preventionof vitaminkdeficiencybleeding: Efficacyof dif- ferent multiple oral dose schedules of vitamin k
-
Cornelissen, M., Von Kries, R., Loughnan, P., Schubiger, G. Preventionof vitaminKdeficiencybleeding:efficacyof dif- ferent multiple oral dose schedules of vitamin K. Eur J Pediatr 1997; 156:126-130.
-
(1997)
Eur J Pediatr
, vol.156
, pp. 126-130
-
-
Cornelissen, M.1
Von Kries, R.2
Loughnan, P.3
Schubiger, G.4
-
138
-
-
0031668803
-
A new mixed micellar preparation for oral vitamin k prophylaxis: Randomised controlled comparison with an intramuscular formulation in breast fed infants
-
Greer, F. R., Marshall, S. R, Severson, R. R., et al. A new mixed micellar preparation for oral vitamin K prophylaxis: randomised controlled comparison with an intramuscular formulation in breast fed infants. Arch Dis Child 1998; 79: 300-305.
-
(1998)
Arch Dis Child
, vol.79
, pp. 300-305
-
-
Greer, F.R.1
Marshall, S.R.2
Severson, R.R.3
-
139
-
-
0033159275
-
Oral vitamin k1 prophylaxis for newborns with a new mixed-micellar preparation of phylloquinone: 3 years experience in switzerland
-
Schubiger, G., Stocker, C., Banziger, O., Laubscher, B., Zim- mermann, H. Oral vitamin K1 prophylaxis for newborns with a new mixed-micellar preparation of phylloquinone: 3 years experience in Switzerland. Eur J Pediatr 1999; 158: 599-602.
-
(1999)
Eur J Pediatr
, vol.158
, pp. 599-602
-
-
Schubiger, G.1
Stocker, C.2
Banziger, O.3
Laubscher, B.4
Zim- Mermann, H.5
-
140
-
-
33748260015
-
Disseminated intravascular coagulation
-
Levi, M., ten Cate, H. Disseminated intravascular coagulation. N Engl J Med 1999; 341:586-592.
-
(1999)
N Engl J Med
, vol.341
, pp. 586-592
-
-
Levi, M.1
Ten Cate, H.2
-
141
-
-
0001638069
-
Developmental hemostasis: Relevance to newborns and infants
-
Nathan, D. G., Orkin, S. H., Philadelphia: W. B. Saunders
-
Andrew, M. Developmental hemostasis: relevance to newborns and infants. In Nathan, D. G., Orkin, S. H., eds. HematologyofInfancy and Childhood, Vol.1. Philadelphia: W. B. Saunders, 1998: 114-157.
-
(1998)
Hematologyofinfancy and Childhood
, vol.1
, pp. 114-157
-
-
Andrew, M.1
-
142
-
-
0014468411
-
Recognitionandtreatmentofintravasular coagulation
-
Abildgaard, C. F. Recognitionandtreatmentofintravasular coagulation. J Pediatr 1969; 74: 163-176.
-
(1969)
J Pediatr
, vol.74
, pp. 163-176
-
-
Abildgaard, C.F.1
-
143
-
-
0016140323
-
On the role of disseminated intravascular coagulation on the pathology of birth asphyxia
-
Anderson, J., Brown, J. K., Cockburn, F. On the role of disseminated intravascular coagulation on the pathology of birth asphyxia. Dev Med Child Neurol 1974; 16: 581-591.
-
(1974)
Dev Med Child Neurol
, vol.16
, pp. 581-591
-
-
Anderson, J.1
Brown, J.K.2
Cockburn, F.3
-
144
-
-
0015075188
-
Coagulation studies in severe birth asphyxia
-
Chessells, J., Wigglesworth, J. Coagulation studies in severe birth asphyxia. Arch Dis Child 1971; 46:253-256.
-
(1971)
Arch Dis Child
, vol.46
, pp. 253-256
-
-
Chessells, J.1
Wigglesworth, J.2
-
145
-
-
0021723789
-
Neonatal and maternal hemostasis: Value of molecular markers in the assessment of hemostatic status
-
Suarez, C. R., Menendez, C. E., Walenga, J. M., Fareed, J. Neonatal and maternal hemostasis: value of molecular markers in the assessment of hemostatic status. Semin Thromb Hemost 1984; 10: 280-284.
-
(1984)
Semin Thromb Hemost
, vol.10
, pp. 280-284
-
-
Suarez, C.R.1
Menendez, C.E.2
Walenga, J.M.3
Fareed, J.4
-
146
-
-
0024597069
-
Fibrinopeptide a levels in maternal and newborn plasma
-
Yuen, P. M., Yin, J. A., Lao, T. T. Fibrinopeptide A levels in maternal and newborn plasma. Eur J Obstet Gynecol Reprod Biol 1989; 30: 239-244.
-
(1989)
Eur J Obstet Gynecol Reprod Biol
, vol.30
, pp. 239-244
-
-
Yuen, P.M.1
Yin, J.A.2
Lao, T.T.3
-
147
-
-
0021843183
-
Neonatal and maternal fibrinolysis: Activation at time of birth
-
Suarez, C. R., Walenga, J., Mangogna, L. C., Fareed, J. Neonatal and maternal fibrinolysis: activation at time of birth. Am J Hematol 1985; 19: 365-372.
-
(1985)
Am J Hematol
, vol.19
, pp. 365-372
-
-
Suarez, C.R.1
Walenga, J.2
Mangogna, L.C.3
Fareed, J.4
-
148
-
-
0033427845
-
Replacement therapy with protein c concentrate in infants and adolescents with meningococcal sepsis and purpura ful- minans
-
Ettingshausen, C. E., Veldmann, A., Beeg, T., et al. Replacement therapy with protein C concentrate in infants and adolescents with meningococcal sepsis and purpura ful- minans. Semin Thromb Hemost 1999; 25: 537-541.
-
(1999)
Semin Thromb Hemost
, vol.25
, pp. 537-541
-
-
Ettingshausen, C.E.1
Veldmann, A.2
Beeg, T.3
-
149
-
-
0033854677
-
Protein c substitution in sepsis-associated purpura fulminans
-
Rintala, E., Kauppila, M., Seppala, O. P, etal. Protein C substitution in sepsis-associated purpura fulminans. Crit Care Med 2000; 28: 2373-2378.
-
(2000)
Crit Care Med
, vol.28
, pp. 2373-2378
-
-
Rintala, E.1
Kauppila, M.2
Seppala, O.P.3
-
150
-
-
0015589482
-
Heparin therapy in meningococcal septicaemia
-
Hunter, J. Heparin therapy in meningococcal septicaemia. ArchDis Child 1973; 48: 233-235.
-
(1973)
Archdis Child
, vol.48
, pp. 233-235
-
-
Hunter, J.1
-
151
-
-
0020558727
-
Heparin for infants and children with meningococcal septicemia: Results of a randomized therapeutic trial
-
Haneberg, B., Gutteberg, T. J., Moe, P. J., et al. Heparin for infants and children with meningococcal septicemia: results of a randomized therapeutic trial. NIPH Ann 1983; 6: 43-47.
-
(1983)
NIPH Ann
, vol.6
, pp. 43-47
-
-
Haneberg, B.1
Gutteberg, T.J.2
Moe, P.J.3
-
152
-
-
0015811375
-
Early heparin therapy in 60 children with acute meningococ- cemia: Relationship between clinical manifestations and coagulation abnormalities
-
Blum, D., Fondu, P., Denolin-Reubens, R., Dubois, J. Early heparin therapy in 60 children with acute meningococ- cemia: relationship between clinical manifestations and coagulation abnormalities. Acta Chir Belg 1973; 4: 288-297.
-
(1973)
Acta Chir Belg
, vol.4
, pp. 288-297
-
-
Blum, D.1
Fondu, P.2
Denolin-Reubens, R.3
Dubois, J.4
-
153
-
-
0015623372
-
Heparin therapy in acute meningococ- cemia
-
Hathaway, W. E. Heparin therapy in acute meningococ- cemia. J Pediatr 1991; 82: 900-901.
-
(1991)
J Pediatr
, vol.82
, pp. 900-901
-
-
Hathaway, W.E.1
-
154
-
-
0015386387
-
Coagulation studies in preterm infants with respiratory distress and intracranial hemorrhage
-
Chessells, J., Wigglesworth, J. Coagulation studies in preterm infants with respiratory distress and intracranial hemorrhage. Arch Dis Child 1972; 47:564-570.
-
(1972)
Arch Dis Child
, vol.47
, pp. 564-570
-
-
Chessells, J.1
Wigglesworth, J.2
-
155
-
-
0018686007
-
Activation of coagulation and disseminated intravascular coagulation in the newborn
-
Corrigan, J. Activation of coagulation and disseminated intravascular coagulation in the newborn. Am J Pediatr Hematol Oncol 1979; 1:245-249.
-
(1979)
Am J Pediatr Hematol Oncol
, vol.1
, pp. 245-249
-
-
Corrigan, J.1
-
156
-
-
0022527936
-
Single fetal death in twin gestation
-
Dudley, D. K., D’Alton, M. E. Single fetal death in twin gestation. Semin Perinatol 1986; 10: 65-72.
-
(1986)
Semin Perinatol
, vol.10
, pp. 65-72
-
-
Dudley, D.K.1
D’Alton, M.E.2
-
157
-
-
0024381160
-
Heparin cof actor ii in adults and infants with thrombosis and dic
-
Chuansumrit, A., Manco-Johnson, M. J., Hathaway, W. E. Heparin cof actor II in adults and infants with thrombosis and DIC. Am J Haematol 1989; 31:109-113.
-
(1989)
Am J Haematol
, vol.31
, pp. 109-113
-
-
Chuansumrit, A.1
Manco-Johnson, M.J.2
Hathaway, W.E.3
-
158
-
-
0022908917
-
Low antithrombin iii in neonatal shock: Dic or non-specific protein depletion
-
Schmidt, B. K., Muraji, T., Zipursky, A. Low antithrombin III in neonatal shock: DIC or non-specific protein depletion? Eur J Pediatr 1986; 145:50-03.
-
(1986)
Eur J Pediatr
, vol.145
, pp. 03-50
-
-
Schmidt, B.K.1
Muraji, T.2
Zipursky, A.3
-
159
-
-
0019370235
-
Aclinicaltrial on the early detection and correction of hemostatic defects in selected high-risk neonates
-
Turner, T., Prouse, C., Prescott, R., Cash, J. D.Aclinicaltrial on the early detection and correction of hemostatic defects in selected high-risk neonates. Br J Haematol 1981; 47: 65-75.
-
(1981)
Br J Haematol
, vol.47
, pp. 65-75
-
-
Turner, T.1
Prouse, C.2
Prescott, R.3
Cash, J.D.4
-
160
-
-
0021928014
-
Prevention of intra ventricular haemorrhage by fresh frozen plasma
-
Beverley, D. W., Pitts-Tucker, T., Congdon, J., Arthur, R. J., Tate, I. Prevention of intra ventricular haemorrhage by fresh frozen plasma. ArchDis Child 1985;60:710-713.
-
(1985)
Archdis Child
, vol.60
, pp. 710-713
-
-
Beverley, D.W.1
Pitts-Tucker, T.2
Congdon, J.3
Arthur, R.J.4
Tate, I.5
-
161
-
-
0015541881
-
Controlled trial of fresh frozen plasma in asphyxiated low birthweight infants
-
Hambleton, G., Appleyard, W. J. Controlled trial of fresh frozen plasma in asphyxiated low birthweight infants. Arch Dis Child 1973; 48:31-35.
-
(1973)
Arch Dis Child
, vol.48
, pp. 31-35
-
-
Hambleton, G.1
Appleyard, W.J.2
-
162
-
-
84927972143
-
Effects of fresh frozen plasma infusions on coagulation screening tests in sick neonates
-
Snydor, M. S., Weaver, R. L., Johnson, C. A. Effects of fresh frozen plasma infusions on coagulation screening tests in sick neonates. PediatrRes 1977;11:542.
-
(1977)
Pediatrres
, vol.11
, pp. 542
-
-
Snydor, M.S.1
Weaver, R.L.2
Johnson, C.A.3
-
163
-
-
0018841229
-
Efficiency of heparin in the treatment of newborn infants with respiratory distress syndrome and disseminated intravascular coagulation
-
Gobel, U., vonVoss, H., Jurgens, H., etal. Efficiency of heparin in the treatment of newborn infants with respiratory distress syndrome and disseminated intravascular coagulation. Eur J Pediatr 1980; 133: 47-49.
-
(1980)
Eur J Pediatr
, vol.133
, pp. 47-49
-
-
Gobel, U.1
Vonvoss, H.2
Jurgens, H.3
-
164
-
-
0020077046
-
Controlled study of treatmentfordisseminatedintravascularcoagulationinthe neonate
-
Gross, S., Filston, H., Anderson, J. C. Controlled study of treatmentfordisseminatedintravascularcoagulationinthe neonate. J Pediatr 1982; 100: 445-448.
-
(1982)
J Pediatr
, vol.100
, pp. 445-448
-
-
Gross, S.1
Filston, H.2
Anderson, J.C.3
-
165
-
-
0024756480
-
Successful treatment of an infant with fulminant hepatitis by factor vii concentrate
-
Kawada, Y., Shiiki, M., Miyagawa, T., et al. Successful treatment of an infant with fulminant hepatitis by factor VII concentrate. Rinsho Ketsueki 1989; 30: 1982-1986.
-
Rinsho Ketsueki
, vol.30
, pp. 1982-1986
-
-
Kawada, Y.1
Shiiki, M.2
Miyagawa, T.3
-
166
-
-
0027522777
-
Recombinant activated factor vii in the treatment of bleeding episodes in patients with inherited and acquired bleeding disorders
-
Hedner, U., Glazer, S., Falch, J. Recombinant activated factor VII in the treatment of bleeding episodes in patients with inherited and acquired bleeding disorders. Transfus Med Rev 1993; 7: 78-83.
-
(1993)
Transfus Med Rev
, vol.7
, pp. 78-83
-
-
Hedner, U.1
Glazer, S.2
Falch, J.3
-
167
-
-
0014732565
-
Hemostasis in cyanotic congenital heart disease
-
Ekert, H., Gilchrist, G., Stanton, R., Hammond, D. Hemostasis in cyanotic congenital heart disease. J Pediatr 1970; 76: 221-230.
-
(1970)
J Pediatr
, vol.76
, pp. 221-230
-
-
Ekert, H.1
Gilchrist, G.2
Stanton, R.3
Hammond, D.4
-
168
-
-
0014737779
-
Polycythemiaincyanotic heart disease: A study of altered coagulation
-
Komp, D. M., Sparrow, A. W. Polycythemiaincyanotic heart disease: a study of altered coagulation. J Pediatr 1970; 76: 231-236.
-
(1970)
J Pediatr
, vol.76
, pp. 231-236
-
-
Komp, D.M.1
Sparrow, A.W.2
-
169
-
-
0020589835
-
Defective platelet aggregation in patients undergoing surgical repair of cyanotic congenital heart disease
-
Ware, J. A., Reaves, W. H., Horak, J. K., Solis, R. T. Defective platelet aggregation in patients undergoing surgical repair of cyanotic congenital heart disease. Ann Thorac Surg 1983; 36: 289-294.
-
(1983)
Ann Thorac Surg
, vol.36
, pp. 289-294
-
-
Ware, J.A.1
Reaves, W.H.2
Horak, J.K.3
Solis, R.T.4
-
170
-
-
84993848621
-
Platelet release abnormality and reduced prothrombin levels in children with cyanotic congenital heart disease
-
Ekert, H., Dowling, S. V. Platelet release abnormality and reduced prothrombin levels in children with cyanotic congenital heart disease. Aust Paediatr J 1977; 13: 17-21.
-
(1977)
Aust Paediatr J
, vol.13
, pp. 17-21
-
-
Ekert, H.1
Dowling, S.V.2
-
171
-
-
0031057652
-
Coagulation and fibrinolytic profile of paediatric patients undergoing cardiopulmonary bypass
-
Chan, A. K. C., Leaker, M., Burrows, F. A., et al. Coagulation and fibrinolytic profile of paediatric patients undergoing cardiopulmonary bypass. Thromb Haemost 1997; 77: 270-277.
-
(1997)
Thromb Haemost
, vol.77
, pp. 270-277
-
-
Chan, A.K.C.1
Leaker, M.2
Burrows, F.A.3
-
172
-
-
0025696890
-
Complications of extracorporeal membrane oxygenation in neonates
-
Watson, J. W., Brown, D. M., Lally, K. P, Null, D., Clark, R. Complications of extracorporeal membrane oxygenation in neonates. South Med J 1990; 83: 1262-1265.
-
(1990)
South Med J
, vol.83
, pp. 1262-1265
-
-
Watson, J.W.1
Brown, D.M.2
Lally, K.P.3
Null, D.4
Clark, R.5
-
173
-
-
0031870112
-
Hematological abnormalities in neonatal patients treated with extracorporeal membrane oxygenation (ecmo)
-
Zavadil, D. P, Stammers, A. H., Willett, L. D., et al. Hematological abnormalities in neonatal patients treated with extracorporeal membrane oxygenation (ECMO). J Extra Corpor Technol 1998; 30: 83-90.
-
(1998)
J Extra Corpor Technol
, vol.30
, pp. 83-90
-
-
Zavadil, D.P.1
Stammers, A.H.2
Willett, L.D.3
-
174
-
-
0028215686
-
Cerebrovascular lesions in infants and children dying after extracorporeal membrane oxygenation
-
Jarjour, I., Ahdab-Barmada, M. Cerebrovascular lesions in infants and children dying after extracorporeal membrane oxygenation. Pediatr Neurol 1994; 10: 13-19.
-
(1994)
Pediatr Neurol
, vol.10
, pp. 13-19
-
-
Jarjour, I.1
Ahdab-Barmada, M.2
-
175
-
-
0027234381
-
Ultrasound abnormalities in term infants on ecmo
-
Canady, A. I., Fessler, R. D., Klein, M. D. Ultrasound abnormalities in term infants on ECMO. Pediatr Neurosurg 1993; 19: 202-205.
-
(1993)
Pediatr Neurosurg
, vol.19
, pp. 202-205
-
-
Canady, A.I.1
Fessler, R.D.2
Klein, M.D.3
-
176
-
-
0029024702
-
Coagulation factor deficiencies during initiation of extracorporeal membrane oxygenation
-
McManus, M., Kevy, S., Bower, L. K., Hickey, P. Coagulation factor deficiencies during initiation of extracorporeal membrane oxygenation. J Pediatr 1995; 126:900-904.
-
(1995)
J Pediatr
, vol.126
, pp. 900-904
-
-
McManus, M.1
Kevy, S.2
Bower, L.K.3
Hickey, P.4
-
177
-
-
0033852546
-
The mechanisms of platelet dysfunction during extracorporeal membrane oxygenation in critically ill neonates
-
Cheung, P Y., Sawicki, G., Salas, E., et al. The mechanisms of platelet dysfunction during extracorporeal membrane oxygenation in critically ill neonates. Crit Care Med 2000; 28: 2584-2590.
-
(2000)
Crit Care Med
, vol.28
, pp. 2584-2590
-
-
Cheung, P.Y.1
Sawicki, G.2
Salas, E.3
-
178
-
-
0032986621
-
Predictors of intracranial hemorrhage during neonatal extracorporeal membrane oxygenation
-
Hardart, G. E., Fackler, J. C. Predictors of intracranial hemorrhage during neonatal extracorporeal membrane oxygenation. J Pediatr 1999; 134: 156-159.
-
(1999)
J Pediatr
, vol.134
, pp. 156-159
-
-
Hardart, G.E.1
Fackler, J.C.2
-
179
-
-
0021833566
-
Subependymal germinal matrix hemorrhage in fullterm neonates
-
Hayden, C. K., Shattuck, K. E., Richardson, C. J., et al. Subependymal germinal matrix hemorrhage in fullterm neonates. Pediatrics 1985;75:714-718.
-
(1985)
Pediatrics
, vol.75
, pp. 714-718
-
-
Hayden, C.K.1
Shattuck, K.E.2
Richardson, C.J.3
-
180
-
-
0020418746
-
Intraventricular hemorrhage in the full-term neonate
-
Scher, M.S., Wright, F.S., Lockman, L. A., Thompson, T. R. Intraventricular hemorrhage in the full-term neonate. Arch Neurol 1982; 39: 769-772.
-
(1982)
Arch Neurol
, vol.39
, pp. 769-772
-
-
Scher, M.S.1
Wright, F.S.2
Lockman, L.A.3
Thompson, T.R.4
-
181
-
-
0020610247
-
Congenital hydrocephalus due to prenatal intracranial hemorrhage
-
Jackson, J. C., Blumhagen, J. D. Congenital hydrocephalus due to prenatal intracranial hemorrhage. Pediatrics 1983; 72: 344-346.
-
(1983)
Pediatrics
, vol.72
, pp. 344-346
-
-
Jackson, J.C.1
Blumhagen, J.D.2
-
182
-
-
0018867498
-
Posterior fossa subdural hemorrhage in the newborn
-
Serfontein, G. L., Rom, S., Stein, S. Posterior fossa subdural hemorrhage in the newborn. Pediatrics 1980; 65: 40-43.
-
(1980)
Pediatrics
, vol.65
, pp. 40-43
-
-
Serfontein, G.L.1
Rom, S.2
Stein, S.3
-
183
-
-
0022257733
-
Subdural hemorrhage in utero
-
Gunn, T. R., Mok, P M., Becroft, D. M. Subdural hemorrhage in utero. Pediatrics 1985; 76:605-610.
-
(1985)
Pediatrics
, vol.76
, pp. 605-610
-
-
Gunn, T.R.1
Mok, P.M.2
Becroft, D.M.3
-
184
-
-
0018640873
-
Changes in clinical presentation of term infants with intracranial hemorrhage
-
Cartwright, G. W., Culbertson, K., Schreiner, R. L., Garg, B. P. Changes in clinical presentation of term infants with intracranial hemorrhage. Dev Med Child Neurol 1979; 21: 730-737.
-
(1979)
Dev Med Child Neurol
, vol.21
, pp. 730-737
-
-
Cartwright, G.W.1
Culbertson, K.2
Schreiner, R.L.3
Garg, B.P.4
-
185
-
-
0018562787
-
Intraventricular hemorrhage in the neonate at term
-
Palma, P. A., Miner, M. E., Morriss, F. H., Jr, Adcock, E. W., 3rd, Denson, S. E. Intraventricular hemorrhage in the neonate at term. Am JDis Child 1979; 133: 941-944.
-
(1979)
Am Jdis Child
, vol.133
, pp. 941-944
-
-
Palma, P.A.1
Miner, M.E.2
Morriss, F.H.3
Adcock, E.W.4
Denson, S.E.5
-
186
-
-
0018474132
-
Neonatal seizures, intracerebral hematoma, and subarachnoid hemorrhage in full-term infants
-
Chaplin, E. R., Jr, Goldstein, G. W., Norman, D. Neonatal seizures, intracerebral hematoma, and subarachnoid hemorrhage in full-term infants. Pediatrics 1979; 63: 812-815.
-
(1979)
Pediatrics
, vol.63
, pp. 812-815
-
-
Chaplin, E.R.1
Goldstein, G.W.2
Norman, D.3
-
187
-
-
0019944281
-
Intraventricular hemorrhage in full-term neonates
-
Guekos-Thoeni, U., Boltshauser, E., Willi, U. V. Intraventricular hemorrhage in full-term neonates. Dev Med Child Neurol 1982; 24: 704-705.
-
(1982)
Dev Med Child Neurol
, vol.24
, pp. 704-705
-
-
Guekos-Thoeni, U.1
Boltshauser, E.2
Willi, U.V.3
-
188
-
-
84980313914
-
Intraventricular hemorrhage in term neonates: Diagnosis by ultrasound
-
MacKay, R. J., de Crespigny, L., Murton, L. J., Roy, R. N. Intraventricular hemorrhage in term neonates: diagnosis by ultrasound. Aust Paediatr J 1984;18:205-207.
-
(1984)
Aust Paediatr J
, vol.18
, pp. 205-207
-
-
Mackay, R.J.1
de Crespigny, L.2
Murton, L.J.3
Roy, R.N.4
-
189
-
-
0018695028
-
Ctbrain scanningin neonates: Indications and practices
-
White, L. W. CTbrain scanningin neonates: indications and practices. Appl Radiol 1979; 8: 58-62.
-
(1979)
Appl Radiol
, vol.8
, pp. 58-62
-
-
White, L.W.1
-
190
-
-
0019146086
-
Diagnosis and follow-up of intraventricular and intracerebral hemorrhages by ultrasound studies of infant’s brain through the fontanelles and sutures
-
Bejar, R., Curbelo, V., Coen, R. W., et al. Diagnosis and follow-up of intraventricular and intracerebral hemorrhages by ultrasound studies of infant’s brain through the fontanelles and sutures. Pediatrics 1980; 66: 661-673.
-
(1980)
Pediatrics
, vol.66
, pp. 661-673
-
-
Bejar, R.1
Curbelo, V.2
Coen, R.W.3
-
191
-
-
0019455093
-
Intracranial hem- orrhageinpremature infants: Accuracyin sonographic evaluation
-
Mack, L. A., Wright, K., Hirsch, J. H., etal. Intracranial hem- orrhageinpremature infants: accuracyin sonographic evaluation. Am J Roentgenol 1981;137: 245-250.
-
(1981)
Am J Roentgenol
, vol.137
, pp. 245-250
-
-
Mack, L.A.1
Wright, K.2
Hirsch, J.H.3
-
192
-
-
0020695896
-
Diagnostic accuracy of neonatal brain imaging: A postmortem correlation of computed tomography and ultrasound scans
-
Pape, K. E., Bennett-Britton, S., Szymonowicz, W., et al. Diagnostic accuracy of neonatal brain imaging: A postmortem correlation of computed tomography and ultrasound scans. J Pediatr 1983; 102: 275-280.
-
(1983)
J Pediatr
, vol.102
, pp. 275-280
-
-
Pape, K.E.1
Bennett-Britton, S.2
Szymonowicz, W.3
-
193
-
-
0034243994
-
Periventricular and intraventricular hemorrhage in the premature infant
-
Antoniuk, S., da Silva, R. V. Periventricular and intraventricular hemorrhage in the premature infant. Rev Neurol 2000; 31: 238-243.
-
(2000)
Rev Neurol
, vol.31
, pp. 238-243
-
-
Antoniuk, S.1
Da Silva, R.V.2
-
194
-
-
0030841377
-
The effect of antenatal phenobarbital therapy on neonatal intracranial hemorrhage in preterm infants
-
Shankaran, S., Papil, L. A., Wright, L. L., et al. The effect of antenatal phenobarbital therapy on neonatal intracranial hemorrhage in preterm infants. N Engl J Med 1997; 337: 466-471.
-
(1997)
N Engl J Med
, vol.337
, pp. 466-471
-
-
Shankaran, S.1
Papil, L.A.2
Wright, L.L.3
-
195
-
-
0021940304
-
Cranialultrasound and clinical studies in preterm infants
-
Graziani, L. J., Pasto, M., Stanley, C., etal.Cranialultrasound and clinical studies in preterm infants. J Pediatr 1985; 106:269-276.
-
(1985)
J Pediatr
, vol.106
, pp. 269-276
-
-
Graziani, L.J.1
Pasto, M.2
Stanley, C.3
-
196
-
-
0022387127
-
Relation between periventricular haemorrhage and ischaemic brain lesions diagnosed by ultrasound in very pre-term infants
-
Sinha, S. K., Davies, J. M., Sims, D. G., Chiswick, M. L. Relation between periventricular haemorrhage and ischaemic brain lesions diagnosed by ultrasound in very pre-term infants. Lancet 1985; 2: 1154-1156.
-
(1985)
Lancet
, vol.2
, pp. 1154-1156
-
-
Sinha, S.K.1
Davies, J.M.2
Sims, D.G.3
Chiswick, M.L.4
-
197
-
-
0019467720
-
Neurologic signs in neonatal intraventricular hemorrhage: A correlation with real-time ultrasound
-
Dubowitz, L. M., Levene, M. I., Morante, A., Palmer, P., Dubowitz, V. Neurologic signs in neonatal intraventricular hemorrhage: a correlation with real-time ultrasound. J Pediatr 1981;99:127-133.
-
(1981)
J Pediatr
, vol.99
, pp. 127-133
-
-
Dubowitz, L.M.1
Levene, M.I.2
Morante, A.3
Palmer, P.4
Dubowitz, V.5
-
198
-
-
0020680792
-
Intracerebellar hemorrhage in a premature newborn: Diag- nosisbyreal-time ultrasound and correlationwith autopsy findings
-
Perlman, J. M., Nelson, J. S., McAlister, W. H., Volpe, J. J. Intracerebellar hemorrhage in a premature newborn: diag- nosisbyreal-time ultrasound and correlationwith autopsy findings. Pediatrics 1983; 71:159-162.
-
(1983)
Pediatrics
, vol.71
, pp. 159-162
-
-
Perlman, J.M.1
Nelson, J.S.2
McAlister, W.H.3
Volpe, J.J.4
-
199
-
-
0020625386
-
Incidence, severity and timing of subependymal and intraventricular hemorrhages in preterm infants born inaperinatalunitasdetectedbyserialreal-timeultrasound
-
Dolfin, T., Skidmore, M. B., Fong, K. W., Hoskins, E.M., Shennan, A. T. Incidence, severity and timing of subependymal and intraventricular hemorrhages in preterm infants born inaperinatalunitasdetectedbyserialreal-timeultrasound. Pediatrics 1983; 71: 541-546.
-
(1983)
Pediatrics
, vol.71
, pp. 541-546
-
-
Dolfin, T.1
Skidmore, M.B.2
Fong, K.W.3
Hoskins, E.M.4
Shennan, A.T.5
-
200
-
-
0022994485
-
Intraventricular haemorrhage and periventricular leucomalacia: Ultrasound and autopsy correlation
-
Trounce, J. Q., Fagan, D., Levene, M. I. Intraventricular haemorrhage and periventricular leucomalacia: ultrasound and autopsy correlation. Arch Dis Child 1986; 61: 1203-1207.
-
(1986)
Arch Dis Child
, vol.61
, pp. 1203-1207
-
-
Trounce, J.Q.1
Fagan, D.2
Levene, M.I.3
-
201
-
-
84927951164
-
Intracranial hemorrhage: Pathogenesis and pathology
-
Taeusch, H. W., Ballard, R. A., Avery, M. E., Philadelphia: W. B. Saunders
-
Menkes, J. H. Intracranial hemorrhage: pathogenesis and pathology. In Taeusch, H. W., Ballard, R. A., Avery, M. E., eds. Diseaseof the Newborn. Philadelphia: W. B. Saunders, 1991:422-425.
-
(1991)
Diseaseof the Newborn
, pp. 422-425
-
-
Menkes, J.H.1
-
202
-
-
0021638171
-
Periventricular, intraventricularhem- orrhages in the premature newborn: Update on pathologic features, pathogenesis and possible means of prevention
-
Goddard-Finegold, J.Periventricular, intraventricularhem- orrhages in the premature newborn: update on pathologic features, pathogenesis and possible means of prevention. Arch Neurol 1984; 41: 766-771.
-
(1984)
Arch Neurol
, vol.41
, pp. 766-771
-
-
Goddard-Finegold, J.1
-
203
-
-
0017391960
-
Subependymal germinal matrix and intraventricular hemorrhage in premature infants: Diagnosis by ct
-
Burstein, J., Papile, L., Burstein, R. Subependymal germinal matrix and intraventricular hemorrhage in premature infants: diagnosis by CT. Am J Roentgenol 1977; 128: 9716.
-
(1977)
Am J Roentgenol
, vol.128
, pp. 9716
-
-
Burstein, J.1
Papile, L.2
Burstein, R.3
-
204
-
-
0019405522
-
Neonatal intraventricular hemorrhage
-
Volpe, J. J. Neonatal intraventricular hemorrhage. N Engl J Med 1981; 304: 886-891.
-
(1981)
N Engl J Med
, vol.304
, pp. 886-891
-
-
Volpe, J.J.1
-
205
-
-
0023322526
-
Intraventricular hemorrhage of the preterm neonate
-
Ment, L. R., Duncan, C. C., Ehrenkranz, R. A. Intraventricular hemorrhage of the preterm neonate. Semin Perinatol 1987; 11:132-141.
-
(1987)
Semin Perinatol
, vol.11
, pp. 132-141
-
-
Ment, L.R.1
Duncan, C.C.2
Ehrenkranz, R.A.3
-
206
-
-
0017180317
-
Origin of intraventricular haemorrhage in the preterm infant
-
Hambleton, G., Wigglesworth, J.S. Origin of intraventricular haemorrhage in the preterm infant. Arch Dis Child 1976;51: 651-659.
-
(1976)
Arch Dis Child
, vol.51
, pp. 651-659
-
-
Hambleton, G.1
Wigglesworth, J.S.2
-
207
-
-
0021367870
-
Timing and evolution of periven- tricular haemorrhage in infants weighing 1250 g or less at birth
-
Szymonowicz, W., Yu, V. Y. Timing and evolution of periven- tricular haemorrhage in infants weighing 1250 g or less at birth. Arch Dis Child 1984; 59:7-12.
-
(1984)
Arch Dis Child
, vol.59
, pp. 7-12
-
-
Szymonowicz, W.1
Yu, V.Y.2
-
208
-
-
0021369305
-
Antecedents of periventricular haemorrhage in infants weighing 1250 g or lessat birth
-
Szymonowicz, W., Yu, V. Y., Wilson, F. E. Antecedents of periventricular haemorrhage in infants weighing 1250 g or lessat birth. ArchDis Child 1984; 59:13-17.
-
(1984)
Archdis Child
, vol.59
, pp. 13-17
-
-
Szymonowicz, W.1
Yu, V.Y.2
Wilson, F.E.3
-
209
-
-
0019382378
-
Pneumothorax and cerebral haemorrhage in preterm infants
-
Lipscomb, A. P., Thorburn, R. J., Reynolds, E. O., etal. Pneumothorax and cerebral haemorrhage in preterm infants. Lancet 1981; 1:414-416.
-
(1981)
Lancet
, vol.1
, pp. 414-416
-
-
Lipscomb, A.P.1
Thorburn, R.J.2
Reynolds, E.O.3
-
210
-
-
0019848449
-
Risk factor analysis of intraventricular hemorrhage in low-birth-weight infants
-
Clark, C. E., Clyman, R. I., Roth, R. S., etal. Risk factor analysis of intraventricular hemorrhage in low-birth-weight infants. J Pediatr 1981; 99: 625-628.
-
(1981)
J Pediatr
, vol.99
, pp. 625-628
-
-
Clark, C.E.1
Clyman, R.I.2
Roth, R.S.3
-
211
-
-
0018893137
-
Intracranial hemorrhage in the premature: Its predictive features and outcome
-
Kosmetatos, N., Dinter, C., Williams, M. L., Lourie, H., Berne, A. S. Intracranial hemorrhage in the premature: its predictive features and outcome. Am J Dis Child 1980; 134: 855-859.
-
(1980)
Am J Dis Child
, vol.134
, pp. 855-859
-
-
Kosmetatos, N.1
Dinter, C.2
Williams, M.L.3
Lourie, H.4
Berne, A.S.5
-
212
-
-
0019424446
-
Factors associatedwith periventricular haemorrhage in very lowbirthweight infants
-
Cooke, R. W. Factors associatedwith periventricular haemorrhage in very lowbirthweight infants. Arch Dis Child 1981; 56: 425-431.
-
(1981)
Arch Dis Child
, vol.56
, pp. 425-431
-
-
Cooke, R.W.1
-
213
-
-
0018940923
-
Intraventricular hemorrhage: A prospective evaluation of etiopathogenesis
-
Dykes, F. D., Lazzara, A., Ahmann, P, et al. Intraventricular hemorrhage: a prospective evaluation of etiopathogenesis. Pediatrics 1980; 66: 42-49.
-
(1980)
Pediatrics
, vol.66
, pp. 42-49
-
-
Dykes, F.D.1
Lazzara, A.2
Ahmann, P.3
-
214
-
-
0023109487
-
Clinical impact of neonatal thrombocytopenia
-
Andrew, M., Castle, Y, Saigal, S., Carter, C., Kelton, J. G. Clinical impact of neonatal thrombocytopenia. J Pediatr 1987; 110: 457-464.
-
(1987)
J Pediatr
, vol.110
, pp. 457-464
-
-
Andrew, M.1
Castle, Y.2
Saigal, S.3
Carter, C.4
Kelton, J.G.5
-
215
-
-
0014419974
-
Intracranial haemorrhage and clotting defects in low-birth-weight infants
-
Gray, O. P, Ackerman, A., Fraser, A. J. Intracranial haemorrhage and clotting defects in low-birth-weight infants. Lancet 1968; 1:545-548.
-
(1968)
Lancet
, vol.1
, pp. 545-548
-
-
Gray, O.P.1
Ackerman, A.2
Fraser, A.J.3
-
216
-
-
0030031704
-
Intraventricular hemorrhage in the preterm infant
-
Vohr, B., Ment, L. R. Intraventricular hemorrhage in the preterm infant. Early Hum Dev 1996; 44:1-16.
-
(1996)
Early Hum Dev
, vol.44
, pp. 1-16
-
-
Vohr, B.1
Ment, L.R.2
-
217
-
-
0028062041
-
Elevatedarterialbloodpressureisassociatedwith peri-intraventricular haemorrhage
-
Gronlund, J. U., Korvenranta, H., Kero, P, Jalonen, J., Vali-maki, I.A. Elevatedarterialbloodpressureisassociatedwith peri-intraventricular haemorrhage. Eur J Pediatr 1994;153: 836-841.
-
(1994)
Eur J Pediatr
, vol.153
, pp. 836-841
-
-
Gronlund, J.U.1
Korvenranta, H.2
Kero, P.3
Jalonen, J.4
Vali-Maki, I.A.5
-
218
-
-
0006483401
-
Low superior vena cava flow and intraventricular haemorrhage in preterm infants
-
Fetal Neonatal Ed
-
Kluckow, M., Evans, N. Low superior vena cava flow and intraventricular haemorrhage in preterm infants. Arch Dis Child Fetal Neonatal Ed 2000; 82: F188-F194.
-
(2000)
Arch Dis Child
, vol.82
, pp. F188-F194
-
-
Kluckow, M.1
Evans, N.2
-
219
-
-
0023720028
-
The use of antenatal vitamin k in the prevention of early neonatal intraventricular hemorrhage
-
Morales, W. J., Angel, J. L., O’Brien, W. F., Knuppel, R. A., Marsalisi, F. The use of antenatal vitamin K in the prevention of early neonatal intraventricular hemorrhage. Am J Obstet Gynecol 1988; 159: 774-779.
-
(1988)
Am J Obstet Gynecol
, vol.159
, pp. 774-779
-
-
Morales, W.J.1
Angel, J.L.2
O’Brien, W.F.3
Knuppel, R.A.4
Marsalisi, F.5
-
220
-
-
0023248385
-
Maternallyadministered antenatalvitamin k1: Effect on neonatal prothrombin activity, partial thromboplastin time, and intraventricular hemorrhage
-
Pomerance, J. J., Teal, J. G., Gogdok, J. F., Brown, S., Stewart, M. E. Maternallyadministered antenatalvitamin K1: effect on neonatal prothrombin activity, partial thromboplastin time, and intraventricular hemorrhage. Obstet Gynecol 1987; 70:235-241.
-
(1987)
Obstet Gynecol
, vol.70
, pp. 235-241
-
-
Pomerance, J.J.1
Teal, J.G.2
Gogdok, J.F.3
Brown, S.4
Stewart, M.E.5
-
221
-
-
0024377394
-
Maternal administration of vitamin k does not improve the coagulation profile of preterm infants
-
Kazzi, N. J., Ilagen, M. B., Liang, K. C. Maternal administration of vitamin K does not improve the coagulation profile of preterm infants. Pediatrics 1989; 84:1045-1050.
-
(1989)
Pediatrics
, vol.84
, pp. 1045-1050
-
-
Kazzi, N.J.1
Ilagen, M.B.2
Liang, K.C.3
-
222
-
-
0025323369
-
Blood coagulation findings and the efficacy of factorxiii concentrate in premature infants with intracranial hemorrhages
-
Shirahata, A., Nakamura, T., Shimono, M., Kaneko, M., Tanaka, S. Blood coagulation findings and the efficacy of factorXIII concentrate in premature infants with intracranial hemorrhages. Thromb Res 1990; 57:755-763.
-
(1990)
Thromb Res
, vol.57
, pp. 755-763
-
-
Shirahata, A.1
Nakamura, T.2
Shimono, M.3
Kaneko, M.4
Tanaka, S.5
-
223
-
-
0030871905
-
Antithrombin iii substitution in preterm infants: Effects on intracranial hemorrhage and coagulation parameters
-
Brangenberg, R., Bodensohn, M., Burger, U. Antithrombin III substitution in preterm infants: effects on intracranial hemorrhage and coagulation parameters. Biol Neonate 1997; 72: 76-83.
-
(1997)
Biol Neonate
, vol.72
, pp. 76-83
-
-
Brangenberg, R.1
Bodensohn, M.2
Burger, U.3
-
224
-
-
0027171233
-
Arandomized controlled trial of platelet transfusions in thrombocytopenic premature infants
-
Andrew, M., Caco, C., Vegh, P, etal.Arandomized controlled trial of platelet transfusions in thrombocytopenic premature infants. JPediatr 1993; 123: 285-291.
-
(1993)
Jpediatr
, vol.123
, pp. 285-291
-
-
Andrew, M.1
Caco, C.2
Vegh, P.3
-
225
-
-
0021125480
-
Tranexamic acid in the prevention of periventricular hemorrhage
-
Hensey, O. J., Morgan, M. E., Cooke, R. W. Tranexamic acid in the prevention of periventricular hemorrhage. Arch Dis Child 1984; 59:719-721.
-
(1984)
Arch Dis Child
, vol.59
, pp. 719-721
-
-
Hensey, O.J.1
Morgan, M.E.2
Cooke, R.W.3
-
226
-
-
0021342476
-
Prophylactic ethamsylate for periventricular haemorrhage
-
Cooke, R. W., Morgan, M. E. Prophylactic ethamsylate for periventricular haemorrhage. Arch Dis Child 1984; 59: 8283.
-
(1984)
Arch Dis Child
, vol.59
, pp. 8283
-
-
Cooke, R.W.1
Morgan, M.E.2
-
227
-
-
0022980384
-
Multicentre trial of ethamsylate for prevention of periventricular haemorrhage in very low birthweight infants
-
Benson, J. W. T., Drayton, M. R., Hayward, C. Multicentre trial of ethamsylate for prevention of periventricular haemorrhage in very low birthweight infants. Lancet 1986; 2: 1297-1300.
-
(1986)
Lancet
, vol.2
, pp. 1297-1300
-
-
Benson, J.W.T.1
Drayton, M.R.2
Hayward, C.3
-
228
-
-
0023931917
-
Randomized low dose indomethacin trial for prevention of intraventric- ularhemorrhageinverylowbirthweightneonates
-
Ment, L. R., Duncan, C. C., Ehrenkranz, R. A. Randomized low dose indomethacin trial for prevention of intraventric- ularhemorrhageinverylowbirthweightneonates.JPediatr 1988; 112:948-955.
-
(1988)
Jpediatr
, vol.112
, pp. 948-955
-
-
Ment, L.R.1
Duncan, C.C.2
Ehrenkranz, R.A.3
-
229
-
-
0023933432
-
Administration of indomethacin for the prevention of periventricular- intraventricular hemorrhage in high-risk neonates
-
Hanigan, W. C., Kennedy, G., Roemisch, F., etal.Administration of indomethacin for the prevention of periventricular- intraventricular hemorrhage in high-risk neonates. J Pediatr 1988; 112: 941-947.
-
(1988)
J Pediatr
, vol.112
, pp. 941-947
-
-
Hanigan, W.C.1
Kennedy, G.2
Roemisch, F.3
-
230
-
-
0022572512
-
Early administration of indomethacin to preterm infants
-
Rennie, J. M., Doyle, J., Cooke, R. W. Early administration of indomethacin to preterm infants. Arch Dis Child 1986; 61: 233-238.
-
(1986)
Arch Dis Child
, vol.61
, pp. 233-238
-
-
Rennie, J.M.1
Doyle, J.2
Cooke, R.W.3
-
231
-
-
0028805001
-
Neonatal thrombosis: Report of a prospective canadian and international registry
-
Schmidt, B., Andrew, M. Neonatal thrombosis: report of a prospective Canadian and international registry. Pediatrics 1995; 96: 939-943.
-
(1995)
Pediatrics
, vol.96
, pp. 939-943
-
-
Schmidt, B.1
Andrew, M.2
-
232
-
-
0030857264
-
Neonatal symptomatic thromboembolism in germany: Two year survey
-
Nowak-Gottl, U., von Kries, R., Gobel, U. Neonatal symptomatic thromboembolism in Germany: two year survey. ArchDis Child 1997; 76: F163-F167.
-
(1997)
Archdis Child
, vol.76
, pp. F163-F167
-
-
Nowak-Gottl, U.1
Von Kries, R.2
Gobel, U.3
-
233
-
-
0031896301
-
Factor v leiden and genetic defects of thrombophilia in childhood porencephaly
-
Debus, O., Koch, H. G., Kurlemann, G., etal. Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly. Arch Dis Child Fetal Neonatal Ed 1998;78: F121-F124.
-
(1998)
Arch Dis Child Fetal Neonatal Ed
, vol.78
, pp. F121-F124
-
-
Debus, O.1
Koch, H.G.2
Kurlemann, G.3
-
234
-
-
17944383968
-
Increased prevalence of factor v leiden mutation in neonatal intracranial haemorrhage
-
Melegh, B., Stankovics, J., Kis, A., etal. Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage. Eur JPediatr 1998; 157: 261.
-
(1998)
Eur Jpediatr
, vol.157
, pp. 261
-
-
Melegh, B.1
Stankovics, J.2
Kis, A.3
-
235
-
-
0026591793
-
The protein c anticoagulant pathway
-
Esmon, C. T. The protein C anticoagulant pathway. Arterioscler Thromb 1992; 12:135-145.
-
(1992)
Arterioscler Thromb
, vol.12
, pp. 135-145
-
-
Esmon, C.T.1
-
236
-
-
0027161205
-
Molecular events that control the protein c anticoagulant pathway
-
Esmon, C. T. Molecular events that control the protein C anticoagulant pathway. Thromb Haemost 1993; 70: 29-35.
-
(1993)
Thromb Haemost
, vol.70
, pp. 29-35
-
-
Esmon, C.T.1
-
237
-
-
0028832910
-
The protein c anticoagulant system: Inherited defects as basis for venous thrombosis
-
Dahlback, B. The protein C anticoagulant system: inherited defects as basis for venous thrombosis. Thromb Res 1995; 77: 1-43.
-
(1995)
Thromb Res
, vol.77
, pp. 1-43
-
-
Dahlback, B.1
-
238
-
-
0028959158
-
Inherited thrombophilia: Resistance to activated protein c as a pathogenic factor of venous thromboembolism
-
Dahlback, B. Inherited thrombophilia: resistance to activated protein C as a pathogenic factor of venous thromboembolism. Blood 1995; 85: 607-614.
-
(1995)
Blood
, vol.85
, pp. 607-614
-
-
Dahlback, B.1
-
239
-
-
0030797313
-
The leiden thrombophilia study (lets)
-
Van der Meer, F. J., Koster, T., Vandenbroucke, J. P, Briet, E., Rosendaal, F. R. The Leiden Thrombophilia Study (LETS). Thromb Haemost 1997; 78: 631-635.
-
(1997)
Thromb Haemost
, vol.78
, pp. 631-635
-
-
Van Der Meer, F.J.1
Koster, T.2
Vandenbroucke, J.P.3
Briet, E.4
Rosendaal, F.R.5
-
240
-
-
0030667686
-
Factor v leiden mutation and the risks for thromboembolic disease: A clinical perspective
-
Price, D. T., Ridker, P. M. Factor V Leiden mutation and the risks for thromboembolic disease: a clinical perspective. Annlntern Med 1997; 127: 895-903.
-
(1997)
Annlntern Med
, vol.127
, pp. 895-903
-
-
Price, D.T.1
Ridker, P.M.2
-
241
-
-
0030746618
-
Thrombophilia as a multigenic disorder
-
Seligsohn, U., Zivelin, A. Thrombophilia as a multigenic disorder. Thromb Haemost 1997; 78:297-301.
-
(1997)
Thromb Haemost
, vol.78
, pp. 297-301
-
-
Seligsohn, U.1
Zivelin, A.2
-
242
-
-
0030608860
-
Arg506 to gln mutation in the factor v gene causes poor fibrinolytic response in children after venous occlusion
-
Nowak-Gottl, U., Binder, M., Dubbers, A., et al. Arg506 to Gln mutation in the factor V gene causes poor fibrinolytic response in children after venous occlusion. Thromb Haemost 1997; 78:1115-1118.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1115-1118
-
-
Nowak-Gottl, U.1
Binder, M.2
Dubbers, A.3
-
243
-
-
0000662461
-
Incidence of venous thromboembolism in families with inherited thrombophilia
-
Simioni, P., Sanson, B. J., Prandoni, P, et al. Incidence of venous thromboembolism in families with inherited thrombophilia. Thromb Haemost 1999; 81: 198-202.
-
(1999)
Thromb Haemost
, vol.81
, pp. 198-202
-
-
Simioni, P.1
Sanson, B.J.2
Prandoni, P.3
-
244
-
-
0041798768
-
Resistance to activated protein c (apcr) in children with venous or arterial thromboembolism
-
Nowak-Gottl, U., Koch, H. G., Aschka, I., et al. Resistance to activated protein C (APCR) in children with venous or arterial thromboembolism. Br J Haematol 1996; 92: 992-998.
-
(1996)
Br J Haematol
, vol.92
, pp. 992-998
-
-
Nowak-Gottl, U.1
Koch, H.G.2
Aschka, I.3
-
245
-
-
0030005015
-
Neonatal purpura fulminans in association with factor v r506q mutation
-
Pipe, S. W., Schmaier, A. H., Nichols, W. C., et al. Neonatal purpura fulminans in association with factor V R506Q mutation. JPediatr 1996; 128: 706-709.
-
(1996)
Jpediatr
, vol.128
, pp. 706-709
-
-
Pipe, S.W.1
Schmaier, A.H.2
Nichols, W.C.3
-
246
-
-
0029841485
-
Factor v q 506 mutation in children with thrombosis
-
Gurgey, A., Mesci, L., Renda, Y., et al. Factor V Q 506 mutation in children with thrombosis. Am J Hematol 1996; 53: 37-39.
-
(1996)
Am J Hematol
, vol.53
, pp. 37-39
-
-
Gurgey, A.1
Mesci, L.2
Renda, Y.3
-
247
-
-
0028784755
-
Activated protein c resistance in a neonate with venous thrombosis
-
Kodish, E., Potter, C., Kirschbaum, N. E., Foster, P A. Activated protein C resistance in a neonate with venous thrombosis. J Pediatr 1995; 127: 645-648.
-
(1995)
J Pediatr
, vol.127
, pp. 645-648
-
-
Kodish, E.1
Potter, C.2
Kirschbaum, N.E.3
Foster, P.A.4
-
248
-
-
0029826570
-
Bilateral renal venous thrombosis in a neonate associated with resistance to activated protein c
-
Haffner, D., Wuhl, E., Zieger, B., et al. Bilateral renal venous thrombosis in a neonate associated with resistance to activated protein C. Pediatr Nephrol 1996;10:737-739.
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 737-739
-
-
Haffner, D.1
Wuhl, E.2
Zieger, B.3
-
249
-
-
0031943663
-
Bilateral renal vein thrombosis and venous sinus thrombosis in a neonate with fvmutation (fvleiden)
-
Pohl, M., Zimmerhackl, B., Heinen, F., et al. Bilateral renal vein thrombosis and venous sinus thrombosis in a neonate with FVmutation (FVLeiden). J Pediatr 1998; 132:159-161.
-
(1998)
J Pediatr
, vol.132
, pp. 159-161
-
-
Pohl, M.1
Zimmerhackl, B.2
Heinen, F.3
-
250
-
-
0029850530
-
Common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort, S. R., Rosendaal, F. R., Reitsma, P. H., Bertina, R. M. A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.A.4
-
251
-
-
0033511292
-
Prothrombin g20210a mutation in a child with spinal cord infarction
-
Young, G., Krohn, K. A., Packer, R. J. Prothrombin G20210A mutation in a child with spinal cord infarction. J Pediatr 1999; 134: 777-779.
-
(1999)
J Pediatr
, vol.134
, pp. 777-779
-
-
Young, G.1
Krohn, K.A.2
Packer, R.J.3
-
252
-
-
0031871649
-
Severe thrombophilia in a paediatric patient with end- stage renal disease: Detection of the prothrombin gene g20210a mutation
-
Stier, C., Potzsch, B., Muller-Berghaus, G., Soergel, M., Klaus, G. Severe thrombophilia in a paediatric patient with end- stage renal disease: detection of the prothrombin gene G20210A mutation. Nephrol Dial Transplant 1998;13:2130-2132.
-
(1998)
Nephrol Dial Transplant
, vol.13
, pp. 2130-2132
-
-
Stier, C.1
Potzsch, B.2
Muller-Berghaus, G.3
Soergel, M.4
Klaus, G.5
-
253
-
-
0024449163
-
Antithrombin: Structure, genomic organization, function and inherited deficiency
-
Lane, D.A., Caso, R.Antithrombin: structure, genomic organization, function and inherited deficiency. Baillieres Clin Haematol 1989; 2: 961-998.
-
(1989)
Baillieres Clin Haematol
, vol.2
, pp. 961-998
-
-
Lane, D.A.1
Caso, R.2
-
255
-
-
0016372578
-
Neonatal aortic thrombosis: A possible clinical manifestation of congenital antithrombin 3 deficiency
-
Bjarke, B., Herin, P, Blomback, M. Neonatal aortic thrombosis: a possible clinical manifestation of congenital antithrombin 3 deficiency. Acta Paediatr Scand 1974; 63: 297-301.
-
(1974)
Acta Paediatr Scand
, vol.63
, pp. 297-301
-
-
Bjarke, B.1
Herin, P.2
Blomback, M.3
-
256
-
-
0002805127
-
Diagnose und therapie eines kongenitalen antithrombin iii mangels in der neonatalen periode
-
Schander, K., Niessen, M., Rehm, A., Budde, U., Muller, N. Diagnose und Therapie eines kongenitalen Antithrombin III Mangels in der neonatalen Periode. Blut 1980; 40: 68.
-
(1980)
Blut
, vol.40
, pp. 68
-
-
Schander, K.1
Niessen, M.2
Rehm, A.3
Budde, U.4
Muller, N.5
-
257
-
-
0020383416
-
Familial antithrombin iii deficiency
-
Winter, J. H., Fenech, A., Ridley, W., etal.Familial antithrombin III deficiency. QJMed 1982; 51: 373-395.
-
(1982)
Qjmed
, vol.51
, pp. 373-395
-
-
Winter, J.H.1
Fenech, A.2
Ridley, W.3
-
258
-
-
0023904864
-
Cerebral thrombosis in a newborn with a congenital deficiency of antithrombin iii
-
Brenner, B., Fishman, A., Goldsher, D., Schreibman, D., Tavory, S. Cerebral thrombosis in a newborn with a congenital deficiency of antithrombin III. Am J Hematol 1988; 27: 209-211.
-
(1988)
Am J Hematol
, vol.27
, pp. 209-211
-
-
Brenner, B.1
Fishman, A.2
Goldsher, D.3
Schreibman, D.4
Tavory, S.5
-
259
-
-
0027280487
-
Myocardial infarction in a neonate with hereditary antithrombin iii deficiency
-
Peeters, S., Vandenplas, Y., Jochmans, K., et al. Myocardial infarction in a neonate with hereditary antithrombin III deficiency. Acta Paediatr 1993; 82: 610-613.
-
(1993)
Acta Paediatr
, vol.82
, pp. 610-613
-
-
Peeters, S.1
Vandenplas, Y.2
Jochmans, K.3
-
260
-
-
0028047592
-
Antithrombin-gly 424 arg: A novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis
-
Jochmans, K., Lissens, W., Vervoort, R., etal. Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis. Blood 1994; 83:146-151.
-
(1994)
Blood
, vol.83
, pp. 146-151
-
-
Jochmans, K.1
Lissens, W.2
Vervoort, R.3
-
261
-
-
0027360562
-
Overtight nappy precipitating thrombosis in antithrombin iii deficiency
-
Soutar, R., Marzinotto, V, Andrew, M. Overtight nappy precipitating thrombosis in antithrombin III deficiency. Arch DisChild 1993; 69:599.
-
(1993)
Arch Dischild
, vol.69
, pp. 599
-
-
Soutar, R.1
Marzinotto, V.2
Andrew, M.3
-
262
-
-
0031707087
-
Postmortem dna diagnosis of factor v leiden in a neonate with systemic thrombosis and probable antithrombin deficiency
-
Newman, R. S., Spear, G. S., Kirschbaum, N. Postmortem DNA diagnosis of factor V Leiden in a neonate with systemic thrombosis and probable antithrombin deficiency. Obstet Gynecol 1998; 92: 702-705.
-
(1998)
Obstet Gynecol
, vol.92
, pp. 702-705
-
-
Newman, R.S.1
Spear, G.S.2
Kirschbaum, N.3
-
263
-
-
0002853865
-
Rare hereditarycoagulation factor abnormalities
-
Nathan, D. G., Oski, F. A., Philadelphia: W. B. Saunders
-
Bauer, K. Rare hereditarycoagulation factor abnormalities. In Nathan, D. G., Oski, F. A., eds. HematologyofInfancy and Childhood. Philadelphia: W. B. Saunders, 1998:1660-1675.
-
(1998)
Hematologyofinfancy and Childhood
, pp. 1660-1675
-
-
Bauer, K.1
-
264
-
-
0028083284
-
Homozygous antithrombin deficiency: Report of two new cases (99 leu to phe) associated with arterial and venous thrombosis
-
Chowdhury, V., Lane, D. A., Mille, B., et al. Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis. Thromb Haemost 1994; 72:198-202.
-
(1994)
Thromb Haemost
, vol.72
, pp. 198-202
-
-
Chowdhury, V.1
Lane, D.A.2
Mille, B.3
-
265
-
-
0025764758
-
Novel point mutations leading to type 1 antithrombin deficiency and thrombosis
-
Olds, R. J., Lane, D. A., Ireland, H., et al. Novel point mutations leading to type 1 antithrombin deficiency and thrombosis. Br J Haematol 1991; 78: 408-413.
-
(1991)
Br J Haematol
, vol.78
, pp. 408-413
-
-
Olds, R.J.1
Lane, D.A.2
Ireland, H.3
-
266
-
-
0001924054
-
Two cases of homozygous antithrombin iii deficiency in a family with congenital deficiency of atiii
-
Senzinger, H., Vinazzer, H., Wuerzburg, Germany: Schmitt and Meyer
-
Hakten, M., Deniz, U., Ozbay, G., Ulutin, O. N. Two cases of homozygous antithrombin III deficiency in a family with congenital deficiency of ATIII. In Senzinger, H., Vinazzer, H., eds. Thrombosis and Haemorrhagic Disorders: Proceedings of the 6th International Meeting of the Danubian League Against Thrombosis and Haemorrhagic Disorders. Wuerzburg, Germany: Schmitt and Meyer, 1989: 177.
-
(1989)
Thrombosis and Haemorrhagic Disorders: Proceedings of the 6Th International Meeting of the Danubian League against Thrombosis and Haemorrhagic Disorders
, pp. 177
-
-
Hakten, M.1
Deniz, U.2
Ozbay, G.3
Ulutin, O.N.4
-
267
-
-
15844392091
-
Double heterozygosity in 2 brothers with antithrombin (atiii) defi- ciencydue to the association of arg 47 to his mutation with a9base pair (bp) deletioninexonvi
-
Vidaud, D., Sirieix, M. E., Alhenc-Gelas, M. A double heterozygosity in 2 brothers with antithrombin (ATIII) defi- ciencydue to the association of Arg 47 to His mutation with a9base pair (bp) deletioninexonVI. Thromb Haemost 1991; 65: 838-839.
-
(1991)
Thromb Haemost
, vol.65
, pp. 838-839
-
-
Vidaud, D.1
Sirieix, M.E.2
Alhenc-Gelas, M.A.3
-
268
-
-
0027217289
-
Congenital antithrombin iii deficient neonate treated with antithrombin iii concentrates
-
Shiozaki, A., Arai, T., Izumi, R., Niiya, K., Sakuragawa, N. Congenital antithrombin III deficient neonate treated with antithrombin III concentrates. Thromb Res 1993; 70: 211-216.
-
(1993)
Thromb Res
, vol.70
, pp. 211-216
-
-
Shiozaki, A.1
Arai, T.2
Izumi, R.3
Niiya, K.4
Sakuragawa, N.5
-
269
-
-
0024507770
-
The clinical spectrum of heterozygous protein c deficiency in a large new england kindred
-
Bovill, E. G., Bauer, K. A., Dickerman, J. D., Callas, P, West, B. The clinical spectrum of heterozygous protein C deficiency in a large New England kindred. Blood 1989; 73:712-717.
-
(1989)
Blood
, vol.73
, pp. 712-717
-
-
Bovill, E.G.1
Bauer, K.A.2
Dickerman, J.D.3
Callas, P.4
West, B.5
-
270
-
-
0027465837
-
Increased risk of venous thrombosis in carriers of hereditary protein c deficiencydefect
-
Allaart, C. F., Poort, S. R., Rosendaal, F. R., etal. Increased risk of venous thrombosis in carriers of hereditary protein C deficiencydefect. Lancet 1993; 341:134-138.
-
(1993)
Lancet
, vol.341
, pp. 134-138
-
-
Allaart, C.F.1
Poort, S.R.2
Rosendaal, F.R.3
-
271
-
-
0029876985
-
Inherited thrombophilia: Pathogenesis, clinical syndromes, and management
-
De Stefano, V., Finazzi, G., Mannucci, P. M. Inherited thrombophilia: pathogenesis, clinical syndromes, and management. Blood 1996; 87: 3531-3544.
-
(1996)
Blood
, vol.87
, pp. 3531-3544
-
-
de Stefano, V.1
Finazzi, G.2
Mannucci, P.M.3
-
272
-
-
0027971225
-
Clinical manifestations and management of inherited thrombophilia: Retrospective analysis and follow-up after diagnosis of 238 patientswithcongenitaldeficiencyof antithrombiniii, pro- tein c, protein s
-
De Stefano, V., Leone, G., Mastrangelo, S., etal.Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patientswithcongenitaldeficiencyof antithrombinIII, pro- tein C, protein S. Thromb Haemost 1994; 72:352-358.
-
(1994)
Thromb Haemost
, vol.72
, pp. 352-358
-
-
de Stefano, V.1
Leone, G.2
Mastrangelo, S.3
-
273
-
-
0031674638
-
Prothrombotic disordersininfantsandchildrenwithcerebralthromboem- bolism
-
DeVeber, G., Monagle, P, Chan, A. K. C., etal.Prothrombotic disordersininfantsandchildrenwithcerebralthromboem- bolism. Arch Neurol 1998; 55: 1539-1543.
-
(1998)
Arch Neurol
, vol.55
, pp. 1539-1543
-
-
Deveber, G.1
Monagle, P.2
Chan, A.K.C.3
-
274
-
-
0029801189
-
Ischaemic stroke in infancy and childhood: Role of the arg506 to gln mutation in the factor v gene
-
Nowak-Gottl, U., Strater, R., Dubbers, A., Oleszuk-Raschke, K., Vielhaber, H. Ischaemic stroke in infancy and childhood: role of the Arg506 to Gln mutation in the factor V gene. Blood Coagul Fibrinolysis 1996; 7: 684-688.
-
(1996)
Blood Coagul Fibrinolysis
, vol.7
, pp. 684-688
-
-
Nowak-Gottl, U.1
Strater, R.2
Dubbers, A.3
Oleszuk-Raschke, K.4
Vielhaber, H.5
-
275
-
-
0031835531
-
Cerebral venous sinus thrombosis in infancy and childhood: Role of genetic and acquired risk factors of thrombophilia
-
Vielhaber, H., Ehrenforth, S., Koch, H. G., et al. Cerebral venous sinus thrombosis in infancy and childhood: role of genetic and acquired risk factors of thrombophilia. Eur J Pediatr 1998; 157: 555-560.
-
(1998)
Eur J Pediatr
, vol.157
, pp. 555-560
-
-
Vielhaber, H.1
Ehrenforth, S.2
Koch, H.G.3
-
276
-
-
0030943180
-
Paediatric thrombo-embolism: The influence of nongenetic factors and the role of activated protein c resistance and protein c deficiency
-
Uttenreuther-Fischer, M. M., Vetter, B., Hellmann, C., et al. Paediatric thrombo-embolism: the influence of nongenetic factors and the role of activated protein C resistance and protein C deficiency. Eur J Pediatr 1997; 156:277-281.
-
(1997)
Eur J Pediatr
, vol.156
, pp. 277-281
-
-
Uttenreuther-Fischer, M.M.1
Vetter, B.2
Hellmann, C.3
-
277
-
-
0031444193
-
Thrombosis in congenital deficiencies of at iii, protein c or protein s: A study of 44 children
-
Toumi, N. H., Khaldi, F, Ben Becheur, S., etal. Thrombosis in congenital deficiencies of AT III, protein C or protein S: a study of 44 children. Hematol Cell Ther 1997; 39:295-299.
-
(1997)
Hematol Cell Ther
, vol.39
, pp. 295-299
-
-
Toumi, N.H.1
Khaldi, F.2
Ben Becheur, S.3
-
278
-
-
0023707069
-
Purpura fulminans: A cutaneous manifestation of severe protein c deficiency
-
Auletta, M. J., Headington, J. T. Purpura fulminans: a cutaneous manifestation of severe protein C deficiency. Arch Dermatol 1988; 124:1387-1391.
-
(1988)
Arch Dermatol
, vol.124
, pp. 1387-1391
-
-
Auletta, M.J.1
Headington, J.T.2
-
279
-
-
0025258844
-
Proposed classification and pathologic mechanisms of purpura fulminans and skin necrosis
-
Adcock, D. M., Brozna, J., Marlar, R. A. Proposed classification and pathologic mechanisms of purpura fulminans and skin necrosis. Semin Thromb Hemost 1990; 16: 333-340.
-
(1990)
Semin Thromb Hemost
, vol.16
, pp. 333-340
-
-
Adcock, D.M.1
Brozna, J.2
Marlar, R.A.3
-
280
-
-
0025243394
-
Dermatopathology of skin necrosis associated with purpurafulminans
-
Adcock, D. M., Hicks, M. J. Dermatopathology of skin necrosis associated with purpurafulminans.Semin Thromb Hemost 1990; 16: 283-292.
-
(1990)
Semin Thromb Hemost
, vol.16
, pp. 283-292
-
-
Adcock, D.M.1
Hicks, M.J.2
-
281
-
-
0030000635
-
Purpura fulmi-nans in a patient homozygous for a mutation in the protein c gene: Prenatal diagnosis in a subsequent pregnancy
-
Alessi, M. C., Aillaud, M. F, Paut, O., et al. Purpura fulmi-nans in a patient homozygous for a mutation in the protein C gene: prenatal diagnosis in a subsequent pregnancy. Thromb Haemost 1996; 75: 525-526.
-
(1996)
Thromb Haemost
, vol.75
, pp. 525-526
-
-
Alessi, M.C.1
Aillaud, M.F.2
Paut, O.3
-
282
-
-
0024399901
-
Report on the diagnosis and treatment of homozygous protein c deficiency: ReportOf theworkingpartyonhomozygouspro- tein c deficiency of the icth-subcommittee on protein c and protein s
-
Marlar, R. A., Montgomery, R. R., Broekmans, A. W. Report on the diagnosis and treatment of homozygous protein C deficiency:reportOf theWorkingPartyonHomozygousPro- tein C Deficiency of the ICTH-Subcommittee on Protein C and Protein S. Thromb Haemost 1989; 61: 529-531.
-
(1989)
Thromb Haemost
, vol.61
, pp. 529-531
-
-
Marlar, R.A.1
Montgomery, R.R.2
Broekmans, A.W.3
-
283
-
-
0026409651
-
Treatment of homozygous protein c deficiency and neonatal purpura fulminans with a purified protein c concentrate
-
Dreyfus, M., Magny, J. F, Bridey, F, et al. Treatment of homozygous protein C deficiency and neonatal purpura fulminans with a purified protein C concentrate. N Engl J Med 1991; 325:1565-1568.
-
(1991)
N Engl J Med
, vol.325
, pp. 1565-1568
-
-
Dreyfus, M.1
Magny, J.F.2
Bridey, F.3
-
284
-
-
0031981018
-
Homozygous protein c deficiency: Description of a new mutation and successful treatment with low molecular weight heparin
-
Monagle, P, Andrew, M., Halton, J., et al. Homozygous protein C deficiency: description of a new mutation and successful treatment with low molecular weight heparin. ThrombHaemost 1998; 79: 756-761.
-
(1998)
Thrombhaemost
, vol.79
, pp. 756-761
-
-
Monagle, P.1
Andrew, M.2
Halton, J.3
-
285
-
-
0019332589
-
Regulationof activatedproteinc by a newprotein: A possible function for bovine protein s
-
Walker, F. J. Regulationof activatedproteinC by a newprotein: a possible function for bovine protein S. J Biol Chem 1980; 255: 5521-5524.
-
(1980)
J Biol Chem
, vol.255
, pp. 5521-5524
-
-
Walker, F.J.1
-
286
-
-
0023926222
-
Levels and plasma distribution of free and c4b-bp-bound protein s in human fetuses and full-term newborns
-
Moalic, R, Gruel, Y., Body, G., et al. Levels and plasma distribution of free and C4b-BP-bound protein S in human fetuses and full-term newborns. Thromb Res 1988; 49:471-480.
-
(1988)
Thromb Res
, vol.49
, pp. 471-480
-
-
Moalic, R.1
Gruel, Y.2
Body, G.3
-
287
-
-
0023898148
-
Low total protein s antigen but high protein s activity due to decreased c4b-binding protein in neonates
-
Schwarz, H. P., Muntean, W., Watzke, H., Richter, B., Griffin, J. H. Low total protein S antigen but high protein S activity due to decreased C4b-binding protein in neonates. Blood 1988;71:562-565.
-
(1988)
Blood
, vol.71
, pp. 562-565
-
-
Schwarz, H.P.1
Muntean, W.2
Watzke, H.3
Richter, B.4
Griffin, J.H.5
-
288
-
-
0023227876
-
Hereditary protein s deficiency: Clinical manifestations
-
Engesser, L., Broekmans, A. W., Briet, E., Brommer, E. J., Bertina, R. M. Hereditary protein S deficiency: clinical manifestations. Annlntern Med 1987; 106: 677-682.
-
(1987)
Annlntern Med
, vol.106
, pp. 677-682
-
-
Engesser, L.1
Broekmans, A.W.2
Briet, E.3
Brommer, E.J.4
Bertina, R.M.5
-
289
-
-
0023659157
-
Severe deep vein thrombosis in a 2-year-old child with protein s deficiency
-
De Stefano, V, Leone, G., Ferrelli, R., etal. Severe deep vein thrombosis in a 2-year-old child with protein S deficiency. Thromb Haemost 1987; 58: 10-89.
-
(1987)
Thromb Haemost
, vol.58
, pp. 10-89
-
-
de Stefano, V.1
Leone, G.2
Ferrelli, R.3
-
290
-
-
0026532822
-
Occurrence of arterial thrombosis in a cohort of patients with hereditary deficiency of clotting inhibitors
-
Simioni, P, Zanardi, S., Saracino, A., Girolami, A. Occurrence of arterial thrombosis in a cohort of patients with hereditary deficiency of clotting inhibitors. J Med 1992; 23: 61-74.
-
(1992)
J Med
, vol.23
, pp. 61-74
-
-
Simioni, P.1
Zanardi, S.2
Saracino, A.3
Girolami, A.4
-
291
-
-
0026546573
-
Severe protein s deficiency in a newborn
-
Pegelow, C. H., Ledford, M. Severe protein S deficiency in a newborn. Pediatrics 1992; 89: 674-675.
-
(1992)
Pediatrics
, vol.89
, pp. 674-675
-
-
Pegelow, C.H.1
Ledford, M.2
-
292
-
-
0028175686
-
Homozygous protein s deficiency due to a one base pair deletion that leads to a stop codon in exon iii of the protein s gene
-
Gomez, E., Ledford, M. R., Pegelow, C. H., Reitsma, P. H., Bertina, R. M. Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S gene. Thromb Haemost 1994; 71:723-726.
-
(1994)
Thromb Haemost
, vol.71
, pp. 723-726
-
-
Gomez, E.1
Ledford, M.R.2
Pegelow, C.H.3
Reitsma, P.H.4
Bertina, R.M.5
-
293
-
-
0025244937
-
Neonatal purpura fulminans due to homozygous protein c or protein s deficiences
-
Marlar, R. A., Neuman, A. Neonatal purpura fulminans due to homozygous protein C or protein S deficiences. Semin Thromb Hemost 1990; 16: 299-309.
-
(1990)
Semin Thromb Hemost
, vol.16
, pp. 299-309
-
-
Marlar, R.A.1
Neuman, A.2
-
294
-
-
0025155588
-
Homozygous protein s deficiency in an infant with purpura fulminans
-
Mahasandana, C., Suvatte, V., Chuansumrit, A., et al. Homozygous protein S deficiency in an infant with purpura fulminans. J Pediatr 1990; 117: 750-753.
-
(1990)
J Pediatr
, vol.117
, pp. 750-753
-
-
Mahasandana, C.1
Suvatte, V.2
Chuansumrit, A.3
-
295
-
-
0025064295
-
Neonatal purpura fulminans associated with homozygous protein s deficiency
-
Mahasandana, C., Suvatte, V, Marlar, R. A., et al. Neonatal purpura fulminans associated with homozygous protein S deficiency. Lancet 1990; 335: 61-62.
-
(1990)
Lancet
, vol.335
, pp. 61-62
-
-
Mahasandana, C.1
Suvatte, V.2
Marlar, R.A.3
-
296
-
-
0030832124
-
A family of protein s deficiency including two adults with homozygous deficiency
-
Hui, C. H., Lam, C. C., Sze, C. S. A family of protein S deficiency including two adults with homozygous deficiency. Thromb Haemost 1997; 78:1158-1159.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1158-1159
-
-
Hui, C.H.1
Lam, C.C.2
Sze, C.S.3
-
297
-
-
0030443048
-
Homozygous protein s deficiency: 7-year follow-up
-
Mahasandana, C., Veerakul, G., Tanphaichitr, V S., et al. Homozygous protein S deficiency: 7-year follow-up. Thromb Haemost 1996; 76:1122.
-
(1996)
Thromb Haemost
, vol.76
, pp. 1122
-
-
Mahasandana, C.1
Veerakul, G.2
Tanphaichitr, V.S.3
-
298
-
-
0033490961
-
Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein s deficiency
-
Mintz-Hittner, H. A., Miyashiro, M.J., Knight-Nanan, D. M., O’Malley, R. E., Marlar, R. A. Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency. Ophthalmology 1999; 106: 1525-1530.
-
(1999)
Ophthalmology
, vol.106
, pp. 1525-1530
-
-
Mintz-Hittner, H.A.1
Miyashiro, M.J.2
Knight-Nanan, D.M.3
O’Malley, R.E.4
Marlar, R.A.5
-
299
-
-
0033052054
-
Compound heterozygosity for one novel and one recurrent mutation in a thai patient with severe protein s deficiency
-
Pung-amritt, P, Poort, S. R., Vos, H. L., et al. Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency. Thromb Haemost 1999; 81: 189-192.
-
(1999)
Thromb Haemost
, vol.81
, pp. 189-192
-
-
Pung-Amritt, P.1
Poort, S.R.2
Vos, H.L.3
-
300
-
-
0028216217
-
Umbilical arterial catheter use: Report of an audit conducted by the study group for complications of perinatal care
-
Fletcher, M. A., Brown, D. R., Landers, S., Seguin, J. Umbilical arterial catheter use: report of an audit conducted by the Study Group for Complications of Perinatal Care. Am J Perinatol 1994; 11: 94-99.
-
(1994)
Am J Perinatol
, vol.11
, pp. 94-99
-
-
Fletcher, M.A.1
Brown, D.R.2
Landers, S.3
Seguin, J.4
-
301
-
-
0030227138
-
Umbilical artery catheter blood sampling alters cerebral blood flow velocity in preterm infants
-
Lott, J., Connor, G., Phillips, J. Umbilical artery catheter blood sampling alters cerebral blood flow velocity in preterm infants. J Perinatol 1996; 16:341-345.
-
(1996)
J Perinatol
, vol.16
, pp. 341-345
-
-
Lott, J.1
Connor, G.2
Phillips, J.3
-
302
-
-
0030037857
-
Effect of umbilical artery catheterization in mesenteric hemodynamics
-
Rand, T., Weninger, M., Kohlhauser, C. Effect of umbilical artery catheterization in mesenteric hemodynamics. Pediatr Radiol 1996; 26: 435-438.
-
(1996)
Pediatr Radiol
, vol.26
, pp. 435-438
-
-
Rand, T.1
Weninger, M.2
Kohlhauser, C.3
-
303
-
-
0023676468
-
Neonatal thrombotic disease: Prevention, diagnosis, and treatment
-
Schmidt, B., Andrew, M. Neonatal thrombotic disease: prevention, diagnosis, and treatment. JPediatr 1988; 113:407-410.
-
(1988)
Jpediatr
, vol.113
, pp. 407-410
-
-
Schmidt, B.1
Andrew, M.2
-
304
-
-
0029015192
-
Umbilical venous catheters: Evaluation of radiographs to determine position and associated complications of malpositioned umbilical venous catheters
-
Raval, N. C., Gonzalez, E., Bhat, A. M., Pearlman, S. A., Stefano, J. L. Umbilical venous catheters: evaluation of radiographs to determine position and associated complications of malpositioned umbilical venous catheters. Am J Perinatol 1995; 12: 201-204.
-
(1995)
Am J Perinatol
, vol.12
, pp. 201-204
-
-
Raval, N.C.1
Gonzalez, E.2
Bhat, A.M.3
Pearlman, S.A.4
Stefano, J.L.5
-
305
-
-
0030867042
-
Umbilical venous catheterization and the risk of portal vein thrombosis
-
Schwartz, D. S., Gettner, P. A., Konstantino, M. M., et al. Umbilical venous catheterization and the risk of portal vein thrombosis. JPediatr 1997; 131: 760-762.
-
(1997)
Jpediatr
, vol.131
, pp. 760-762
-
-
Schwartz, D.S.1
Gettner, P.A.2
Konstantino, M.M.3
-
306
-
-
0016702177
-
Portal hypertension in children following neonatal umbilical disorders
-
Obladen, M., Ernst, D., Feist, D., Wille, L. Portal hypertension in children following neonatal umbilical disorders. J Perinat Med 1975; 3: 101-104.
-
(1975)
J Perinat Med
, vol.3
, pp. 101-104
-
-
Obladen, M.1
Ernst, D.2
Feist, D.3
Wille, L.4
-
307
-
-
0006301956
-
Portal hypertension following exchange transfusion through the umbilical vein
-
Tizard, J. P M. Portal hypertension following exchange transfusion through the umbilical vein. Proc Soc Exp Biol Med 1962; 55: 772.
-
(1962)
Proc Soc Exp Biol Med
, vol.55
, pp. 772
-
-
Tizard, J.P.M.1
-
308
-
-
0001757134
-
The aetiology of portal vein thrombosis with particular reference to the role of infection and exchange transfusion
-
Thompson, E. M., Sherlock, S. The aetiology of portal vein thrombosis with particular reference to the role of infection and exchange transfusion. QJMed 1964; 33:465.
-
(1964)
Qjmed
, vol.33
, pp. 465
-
-
Thompson, E.M.1
Sherlock, S.2
-
309
-
-
0016279717
-
Splenic vein thrombosis with oesophageal varices: A late complication of umbilical vein catheterization
-
Vos, L. J., Potocky, V, Broker, F. H., et al. Splenic vein thrombosis with oesophageal varices: a late complication of umbilical vein catheterization. Ann Surg 1974; 180:152-156.
-
(1974)
Ann Surg
, vol.180
, pp. 152-156
-
-
Vos, L.J.1
Potocky, V.2
Broker, F.H.3
-
310
-
-
0019515841
-
Congenital hypertension due to unilateral renal vein thrombosis
-
Evans, D. J., Silverman, M., Bowley, N. B. Congenital hypertension due to unilateral renal vein thrombosis. Arch Dis Child 1981; 56: 306-308.
-
(1981)
Arch Dis Child
, vol.56
, pp. 306-308
-
-
Evans, D.J.1
Silverman, M.2
Bowley, N.B.3
-
311
-
-
0031672239
-
Central venous catheter related thrombosis in children: Analysis of the canadian registry of venous thromboembolic complications
-
Massicotte, M. P., Dix, D., Monagle, P., Adams, M., Andrew, M. Central venous catheter related thrombosis in children: analysis of the Canadian Registry of Venous Thromboembolic Complications. JPediatr 1998; 133: 770-776.
-
(1998)
Jpediatr
, vol.133
, pp. 770-776
-
-
Massicotte, M.P.1
Dix, D.2
Monagle, P.3
Adams, M.4
Andrew, M.5
-
312
-
-
0032103168
-
Deep venous thrombosis of the upper limbs: A propos of 49 cases
-
Marie, I., Levesque, H., Cailleux, N., et al. Deep venous thrombosis of the upper limbs: a propos of 49 cases. Rev Medlnterne 1998; 19: 399-408.
-
(1998)
Rev Medlnterne
, vol.19
, pp. 399-408
-
-
Marie, I.1
Levesque, H.2
Cailleux, N.3
-
313
-
-
0021720604
-
Complications of superior versus inferior vena cava occlusion in infants receiving central total parenteral nutrition
-
Mulvihill, S. J., Fonkalsrud, E. W. Complications of superior versus inferior vena cava occlusion in infants receiving central total parenteral nutrition. J Pediatr Surg 1984; 19:752-757.
-
(1984)
J Pediatr Surg
, vol.19
, pp. 752-757
-
-
Mulvihill, S.J.1
Fonkalsrud, E.W.2
-
314
-
-
0021274350
-
Fatal pulmonary embolism following removal of a central venous catheter
-
Rockoff, M. A., Gang, D. L., Vacanti, J. P. Fatal pulmonary embolism following removal of a central venous catheter. J Pediatr Surg 1984; 19: 307-309.
-
(1984)
J Pediatr Surg
, vol.19
, pp. 307-309
-
-
Rockoff, M.A.1
Gang, D.L.2
Vacanti, J.P.3
-
315
-
-
0029439853
-
Venous catheter thrombus formation and pulmonaryembolism in children
-
Derish, M. T., Smith, D. W., Frankel, L. R. Venous catheter thrombus formation and pulmonaryembolism in children. Pediatr Pulmonol 1995; 20: 349-354.
-
(1995)
Pediatr Pulmonol
, vol.20
, pp. 349-354
-
-
Derish, M.T.1
Smith, D.W.2
Frankel, L.R.3
-
316
-
-
0029445589
-
Deep venous lines and thromboembolism
-
Ament, J., Newth, C. J. Deep venous lines and thromboembolism. Pediatr Pulmonol 1995; 20: 347-348.
-
(1995)
Pediatr Pulmonol
, vol.20
, pp. 347-348
-
-
Ament, J.1
Newth, C.J.2
-
317
-
-
0028008663
-
Venous thromboembolic complications (vte) in children: First analyses of the canadian registry of vte
-
Andrew, M., David, M., Adams, M., et al. Venous thromboembolic complications (VTE) in children: first analyses of the Canadian Registry of VTE. Blood 1994; 83: 1251-1257.
-
(1994)
Blood
, vol.83
, pp. 1251-1257
-
-
Andrew, M.1
David, M.2
Adams, M.3
-
318
-
-
0034049880
-
Outcome of pediatric thromboembolic disease: A report from the canadian childhood thrombophilia registry
-
Monagle, P, Adams, M., Mahoney, M., et al. Outcome of pediatric thromboembolic disease: a report from the Canadian Childhood Thrombophilia Registry. Pediatr Res 2000; 47: 763-766.
-
(2000)
Pediatr Res
, vol.47
, pp. 763-766
-
-
Monagle, P.1
Adams, M.2
Mahoney, M.3
-
319
-
-
0028271561
-
Efficacy and safety of heparin anticoagulation for neonatal renal vein thrombosis
-
Nuss, R., Hays, T., Manco-Johnson, M. Efficacy and safety of heparin anticoagulation for neonatal renal vein thrombosis. Am J Pediatr Hematol Oncol 1994; 16:127-131.
-
(1994)
Am J Pediatr Hematol Oncol
, vol.16
, pp. 127-131
-
-
Nuss, R.1
Hays, T.2
Manco-Johnson, M.3
-
320
-
-
0030734897
-
The ultrasound appearances of neonatal renal vein thrombosis
-
Hibbert, J., Howlett, D. C., Greenwood, K. L., MacDonald, L. M., Saunders, A. J. The ultrasound appearances of neonatal renal vein thrombosis. Br J Radiol 1997;70:1191-1194.
-
(1997)
Br J Radiol
, vol.70
, pp. 1191-1194
-
-
Hibbert, J.1
Howlett, D.C.2
Greenwood, K.L.3
Macdonald, L.M.4
Saunders, A.J.5
-
321
-
-
0031912301
-
Acute bilateral renal vein thrombosis complicating netherton syndrome
-
Pohl, M., Zimmerhackl, L. B., Hausser, I., etal.Acute bilateral renal vein thrombosis complicating Netherton syndrome. Eur J Pediatr 1998; 157:157-160.
-
(1998)
Eur J Pediatr
, vol.157
, pp. 157-160
-
-
Pohl, M.1
Zimmerhackl, L.B.2
Hausser, I.3
-
322
-
-
0020321208
-
Bilateral renal vein thrombosis in infancy and childhood
-
Gonzalez, R., Schwartz, S., Sheldon, C. A., Fraley, E. E. Bilateral renal vein thrombosis in infancy and childhood. Urol Clin North Am 1982; 9: 279-283.
-
(1982)
Urol Clin North Am
, vol.9
, pp. 279-283
-
-
Gonzalez, R.1
Schwartz, S.2
Sheldon, C.A.3
Fraley, E.E.4
-
323
-
-
0026058442
-
Renal venous thrombosis in infancy: Long-term follow-up
-
Mocan, H., Beattie, T. J., Murphy, A. Renal venous thrombosis in infancy: long-term follow-up. Pediatr Nephrol 1991; 5: 45-49.
-
(1991)
Pediatr Nephrol
, vol.5
, pp. 45-49
-
-
Mocan, H.1
Beattie, T.J.2
Murphy, A.3
-
324
-
-
0022633899
-
Treatment of grafts and major vessel thrombosis with low-dose streptokinase in children
-
Leblanc, J. G., Culham, J. A., Chan, K. W., et al. Treatment of grafts and major vessel thrombosis with low-dose streptokinase in children. Ann Thorac Surg 1986; 41:630-635.
-
(1986)
Ann Thorac Surg
, vol.41
, pp. 630-635
-
-
Leblanc, J.G.1
Culham, J.A.2
Chan, K.W.3
-
325
-
-
0021364386
-
Echographic diagnosis of neona- tal renal venous thrombosis
-
Metreweli, C., Pearson, R. Echographic diagnosis of neona- tal renal venous thrombosis. Pediatr Radiol 1984; 14:105-108.
-
(1984)
Pediatr Radiol
, vol.14
, pp. 105-108
-
-
Metreweli, C.1
Pearson, R.2
-
326
-
-
0023253776
-
Neonatal limb gangrene and renalvein thrombosis: Case report with review of literature
-
Nazer, H., Rajab, A. A., Qaryouti, S., etal.Neonatal limb gangrene and renalvein thrombosis: case report with review of literature. Eur J Pediatr 1987; 146:429-431.
-
(1987)
Eur J Pediatr
, vol.146
, pp. 429-431
-
-
Nazer, H.1
Rajab, A.A.2
Qaryouti, S.3
-
327
-
-
0026528083
-
Obstructive aortic and renal thrombosis in the newborn-spontaneous recovery
-
Munoz-Anizpe, R., Walsh, R. F., Edge, W. Obstructive aortic and renal thrombosis in the newborn-spontaneous recovery. Pediatr Nephrol 1992; 6:190-191.
-
(1992)
Pediatr Nephrol
, vol.6
, pp. 190-191
-
-
Munoz-Anizpe, R.1
Walsh, R.F.2
Edge, W.3
-
328
-
-
0024305561
-
The asso- ciationof nephrotic syndrome and renalvein thrombosis: A clinicopathologicalanalysisof eightpediatricpatients
-
Tinaztepe, K., Buyan, N., Tinaztepe, B., Akkok, N. The asso- ciationof nephrotic syndrome and renalvein thrombosis: a clinicopathologicalanalysisof eightpediatricpatients. Turk J Pediatr 1989; 31:1-8.
-
(1989)
Turk J Pediatr
, vol.31
, pp. 1-8
-
-
Tinaztepe, K.1
Buyan, N.2
Tinaztepe, B.3
Akkok, N.4
-
329
-
-
0024397148
-
Thrombus calcification of renal vein in neonate: Ultrasound and ct diagnosis
-
Starinsky, R., Graif, M., Lotan, D., Kessler, A. Thrombus calcification of renal vein in neonate: ultrasound and CT diagnosis. JComputAssist Tomogr 1989; 13:545-546.
-
(1989)
Jcomputassist Tomogr
, vol.13
, pp. 545-546
-
-
Starinsky, R.1
Graif, M.2
Lotan, D.3
Kessler, A.4
-
330
-
-
0016613441
-
Thrombectomy for neanatal renal vein thrombosis
-
Thompson, I. M., Schneider, R., Lababidi, Z. Thrombectomy for neanatal renal vein thrombosis. J Urol 1975; 113: 396-399.
-
(1975)
J Urol
, vol.113
, pp. 396-399
-
-
Thompson, I.M.1
Schneider, R.2
Lababidi, Z.3
-
331
-
-
0015633156
-
Consumptive coagulopathy with renalvein thrombosis
-
Renfield, M. L., Kraybill, E. N. Consumptive coagulopathy with renalvein thrombosis. JPediatr 1973; 82:1054-1056.
-
(1973)
Jpediatr
, vol.82
, pp. 1054-1056
-
-
Renfield, M.L.1
Kraybill, E.N.2
-
332
-
-
84927959296
-
Renal venous thrombosis in infancy
-
Oliver, W. J., Kelsch, R. C. Renal venous thrombosis in infancy. Pediatrics Rev 1982; 4: 61-66.
-
(1982)
Pediatrics Rev
, vol.4
, pp. 61-66
-
-
Oliver, W.J.1
Kelsch, R.C.2
-
333
-
-
0014847575
-
Nonsurgical manage- mentofthrombosisof bilateralrenalveinsandinferiorvena cava in a newborn infant
-
Seeler, R.A., Kapadia, P, Moncado, R. Nonsurgical manage- mentofthrombosisof bilateralrenalveinsandinferiorvena cava in a newborn infant. Clin Pediatr 1970; 9: 543-547.
-
(1970)
Clin Pediatr
, vol.9
, pp. 543-547
-
-
Seeler, R.A.1
Kapadia, P.2
Moncado, R.3
-
334
-
-
84971583538
-
Thrombectomy for renal venous thrombosis in infant of diabetic mother
-
Lowry, M. F., Mann, J. R., Abrams, L. D., Chance, G. W. Thrombectomy for renal venous thrombosis in infant of diabetic mother. BrMed J 1970;3:687.
-
(1970)
Brmed J
, vol.3
, pp. 687
-
-
Lowry, M.F.1
Mann, J.R.2
Abrams, L.D.3
Chance, G.W.4
-
335
-
-
0022979598
-
Spontaneous neonatal renal vein thrombosis
-
Fielding, G. A., Masel, J., Leditschke, J. F. Spontaneous neonatal renal vein thrombosis. Aust N Z J Surg 1986; 56: 485-488.
-
(1986)
Aust N Z J Surg
, vol.56
, pp. 485-488
-
-
Fielding, G.A.1
Masel, J.2
Leditschke, J.F.3
-
336
-
-
0014951126
-
Nonoperative treatment of unilateral renal vein thrombosis in the newborn
-
Belman, A. B., Susmano, D. F., Burden, J. J., Kaplan, G. W. Nonoperative treatment of unilateral renal vein thrombosis in the newborn. J Am Med Assoc 1970; 211: 1165-1168.
-
(1970)
J am Med Assoc
, vol.211
, pp. 1165-1168
-
-
Belman, A.B.1
Susmano, D.F.2
Burden, J.J.3
Kaplan, G.W.4
-
337
-
-
0030758713
-
Bilateral renal vein thrombosis in a newborn: A case of prenatal renal vein thrombosis
-
Cozzolino, D. J., Cendron, M. Bilateral renal vein thrombosis in a newborn: a case of prenatal renal vein thrombosis. Urology 1997; 50: 128-131.
-
(1997)
Urology
, vol.50
, pp. 128-131
-
-
Cozzolino, D.J.1
Cendron, M.2
-
338
-
-
0025761598
-
In utero arterial embolism from renal vein thrombosis with successful postnatal thrombolytic therapy
-
Duncan, B., Adzick, N. S., Longaker, M., et al. In utero arterial embolism from renal vein thrombosis with successful postnatal thrombolytic therapy. J PediatrSurg 1991; 26: 741-743.
-
(1991)
J Pediatrsurg
, vol.26
, pp. 741-743
-
-
Duncan, B.1
Adzick, N.S.2
Longaker, M.3
-
339
-
-
0024585263
-
Ultrasound demonstration of prenatal renal vein thrombosis
-
Sanders, L., Jequier, S. Ultrasound demonstration of prenatal renal vein thrombosis. Pediatr Radiol 1989; 19: 133-135.
-
(1989)
Pediatr Radiol
, vol.19
, pp. 133-135
-
-
Sanders, L.1
Jequier, S.2
-
340
-
-
0025160095
-
Perinatal renal vein thrombosis
-
Lalmand, B., Avni, E. F., Nasr, A., Ketelbant, P., Struyven, J. Perinatal renal vein thrombosis. J Ultrasound Med 1990; 9: 437-442.
-
(1990)
J Ultrasound Med
, vol.9
, pp. 437-442
-
-
Lalmand, B.1
Avni, E.F.2
Nasr, A.3
Ketelbant, P.4
Struyven, J.5
-
341
-
-
0021675830
-
Renalveinthrombosis in stillborn infant of diabetic mother
-
Al-Samarrai, S. F., Kato, A., Urano, Y. Renalveinthrombosis in stillborn infant of diabetic mother. Acta Pathol Jpn 1984; 34: 1441-1447.
-
(1984)
Acta Pathol Jpn
, vol.34
, pp. 1441-1447
-
-
Al-Samarrai, S.F.1
Kato, A.2
Urano, Y.3
-
342
-
-
0022740631
-
Renalandaxillary thrombosis in an infant of a diabetic mother
-
Tekinalp, G., Oran, O., Erturk, G., Yetgin, S. Renalandaxillary thrombosis in an infant of a diabetic mother. Turk J Pediatr 1986; 28:191-194.
-
(1986)
Turk J Pediatr
, vol.28
, pp. 191-194
-
-
Tekinalp, G.1
Oran, O.2
Erturk, G.3
Yetgin, S.4
-
343
-
-
0021049215
-
Dehydra- tion, renalveinthrombosis, and hyperkalemicrenaltubular acidosis in a newborn
-
Glassock, R. J., Duffy, J., Kodroff, M. B., Chan, J. C. Dehydra- tion, renalveinthrombosis, and hyperkalemicrenaltubular acidosis in a newborn. Am JNephrol 1983; 3:329-337.
-
(1983)
Am Jnephrol
, vol.3
, pp. 329-337
-
-
Glassock, R.J.1
Duffy, J.2
Kodroff, M.B.3
Chan, J.C.4
-
344
-
-
0016682882
-
Compression of superior sagittal sinus by neonatal calvarial molding
-
Newton, T. H., Gooding, C. A. Compression of superior sagittal sinus by neonatal calvarial molding. Neuroradiology 1975; 115:635-639.
-
(1975)
Neuroradiology
, vol.115
, pp. 635-639
-
-
Newton, T.H.1
Gooding, C.A.2
-
345
-
-
84927954276
-
Canadian pediatric ischemic stroke registry: Analysis i
-
DeVeber, G., Andrew, M. Canadian pediatric ischemic stroke Registry: analysis I. PediatrRes 1994; 35:379A.
-
(1994)
Pediatrres
, vol.379A
, pp. 35
-
-
Deveber, G.1
Andrew, M.2
-
346
-
-
0026737480
-
Neonatal idiopathic cerebral venous thrombosis: An unrecognized cause of transient seizuresorlethargy
-
Rivkin, M. J., Anderson, M. L., Kaye, E. M. Neonatal idiopathic cerebral venous thrombosis: an unrecognized cause of transient seizuresorlethargy. AnnNeurol 1992; 32:51-56.
-
(1992)
Annneurol
, vol.32
, pp. 51-56
-
-
Rivkin, M.J.1
Anderson, M.L.2
Kaye, E.M.3
-
347
-
-
0024308980
-
Neonatal dural sinus thrombosis
-
Shevell, M. I., Silver, K., O’Gorman, A. M., Watters, G. V, Montes, J. L. Neonatal dural sinus thrombosis. Pediatr Neurol 1989; 5:161-165.
-
(1989)
Pediatr Neurol
, vol.5
, pp. 161-165
-
-
Shevell, M.I.1
Silver, K.2
O’Gorman, A.M.3
Watters, G.V.4
Montes, J.L.5
-
348
-
-
0026523432
-
Cerebral venous thrombosis in neonates and children
-
Barron, T. F., Gusnard, D. A., Zimmerman, R. A., Clancy, R. R. Cerebral venous thrombosis in neonates and children. Pediatr Neurol 1992; 8: 112-116.
-
(1992)
Pediatr Neurol
, vol.8
, pp. 112-116
-
-
Barron, T.F.1
Gusnard, D.A.2
Zimmerman, R.A.3
Clancy, R.R.4
-
349
-
-
12244251511
-
Clinical findings and differential diagnosis of cerebral vein thrombosis
-
Einhaupl, K., ed
-
Hartmann, A., Wappenschmidt, J., Solymosi, L., Brassel, J. Clinical findings and differential diagnosis of cerebral vein thrombosis. In Einhaupl, K., ed. CerebralSinus Thrombosis: Experimental and Clinical Aspects.NewYork: PlenumPress, 1987:171-185.
-
(1987)
Cerebralsinus Thrombosis: Experimental and Clinical Aspects.Newyork: Plenumpress
, pp. 171-185
-
-
Hartmann, A.1
Wappenschmidt, J.2
Solymosi, L.3
Brassel, J.4
-
350
-
-
0026558334
-
Pediatric magnetic resonance angiography: Assessment of stroke
-
Zimmerman, R. A., Bogdan, A. R., Gusnard, D. A. Pediatric magnetic resonance angiography: assessment of stroke. Cardiovasc Intervent Radiol 1992; 15: 60-64.
-
(1992)
Cardiovasc Intervent Radiol
, vol.15
, pp. 60-64
-
-
Zimmerman, R.A.1
Bogdan, A.R.2
Gusnard, D.A.3
-
351
-
-
0022587916
-
High field mrimagingof cerebralvenousthrombosis
-
Macchi, PJ., Grossman, R. I., Gomori, J. M., etal. High field MRimagingof cerebralvenousthrombosis.J Comput Assist Tomogr 1986; 10:10-15.
-
(1986)
J Comput Assist Tomogr
, vol.10
, pp. 10-15
-
-
Macchi, P.J.1
Grossman, R.I.2
Gomori, J.M.3
-
352
-
-
0026440744
-
Children with cerebral venous thrombosis diagnosed with magnetic resonance imaging and magnetic resonance angiography
-
Medlock, M. D., Olivero, W. C., Hanigan, W. C., Wright, R. M., Winek, S. J. Children with cerebral venous thrombosis diagnosed with magnetic resonance imaging and magnetic resonance angiography. Neurosurgery 1992; 31: 870-876.
-
(1992)
Neurosurgery
, vol.31
, pp. 870-876
-
-
Medlock, M.D.1
Olivero, W.C.2
Hanigan, W.C.3
Wright, R.M.4
Winek, S.J.5
-
353
-
-
0029033448
-
Character- ization of superior sagittal sinus blood flow velocity using color flow doppler in neonates and infants
-
Bezinque, S. L., Slovis, T. L., Touchette, A. S., etal.Character- ization of superior sagittal sinus blood flow velocity using color flow Doppler in neonates and infants. Pediatr Radiol 1995; 25:175-179.
-
(1995)
Pediatr Radiol
, vol.25
, pp. 175-179
-
-
Bezinque, S.L.1
Slovis, T.L.2
Touchette, A.S.3
-
354
-
-
0024270529
-
Heparinclearance and ex vivo recovery in newborn piglets and adult pigs
-
Andrew, M., Of osu, F., Schmidt, B., etal. Heparinclearance and ex vivo recovery in newborn piglets and adult pigs. Thromb Res 1988; 52: 517-527.
-
(1988)
Thromb Res
, vol.52
, pp. 517-527
-
-
Andrew, M.1
Ofosu, F.2
Schmidt, B.3
-
355
-
-
0019510359
-
Heparin clearance in the newborn
-
McDonald, M. M., Jacobson, L. J., Hay, W. W., Hathaway, W. E. Heparin clearance in the newborn. Pediatr Res 1981; 15: 1015-1018.
-
(1981)
Pediatr Res
, vol.15
, pp. 1015-1018
-
-
McDonald, M.M.1
Jacobson, L.J.2
Hay, W.W.3
Hathaway, W.E.4
-
356
-
-
84927979033
-
Heparin is cleared faster in children with congenital heart disease thanadults
-
Turner Gomes, S., Nitschmann, E., Benson, L., Burrows, P., Andrew, M. Heparin is cleared faster in children with congenital heart disease thanadults. JAm Coll Cardiol 1993; 21: 59a.
-
(1993)
Jam Coll Cardiol
, vol.59a
, pp. 21
-
-
Turner Gomes, S.1
Nitschmann, E.2
Benson, L.3
Burrows, P.4
Andrew, M.5
-
357
-
-
0026434005
-
Heparin
-
Hirsh, J. Heparin. N Engl JMed 1991; 324:1565-1574.
-
(1991)
N Engl Jmed
, vol.324
, pp. 1565-1574
-
-
Hirsh, J.1
-
358
-
-
0028047498
-
Heparin therapy in pediatric patients: A prospective cohort study
-
Andrew, M., Marzinotto, V., Massicotte, P., et al Heparin therapy in pediatric patients: a prospective cohort study. PediatrRes 1994; 35: 78-83.
-
(1994)
Pediatrres
, vol.35
, pp. 78-83
-
-
Andrew, M.1
Marzinotto, V.2
Massicotte, P.3
-
359
-
-
0026022024
-
A standard heparin nomogram for the management of heparin therapy
-
Cruickshank, M. K., Levine, M. N., Hirsh, J., Roberts, R., Siguenza, M. A standard heparin nomogram for the management of heparin therapy. ArchIntern Med 1991; 151:333-337.
-
(1991)
Archintern Med
, vol.151
, pp. 333-337
-
-
Cruickshank, M.K.1
Levine, M.N.2
Hirsh, J.3
Roberts, R.4
Siguenza, M.5
-
360
-
-
0026593425
-
Low molecular weight heparin
-
Hirsh, J., Levine, M. Low molecular weight heparin. Blood 1992; 79:1-7.
-
(1992)
Blood
, vol.79
, pp. 1-7
-
-
Hirsh, J.1
Levine, M.2
-
361
-
-
0030858230
-
Low molecular weight heparins
-
Weitz, J. I. Low molecular weight heparins. N Engl J Med 1997; 337: 688-698.
-
(1997)
N Engl J Med
, vol.337
, pp. 688-698
-
-
Weitz, J.I.1
-
362
-
-
0002894293
-
Dose finding and pharmacokinetics of prophylactic doses of a low molecular weight heparin (reviparintm) in pediatric patients
-
Massicotte, M. P., Marzinotto, V, Julian, J., etal. Dose finding and pharmacokinetics of prophylactic doses of a low molecular weight heparin (reviparinTM) in pediatric patients. Blood 1999; 94 (Suppl 1): 27a.
-
(1999)
Blood
, vol.94
, pp. 27a
-
-
Massicotte, M.P.1
Marzinotto, V.2
Julian, J.3
-
363
-
-
0029929402
-
Low-molecular-weight heparin in pediatric patients with thrombotic disease: A dose finding study
-
Massicotte, P., Adams, M., Marzinotto, V, Brooker, L. A., Andrew, M. Low-molecular-weight heparin in pediatric patients with thrombotic disease: a dose finding study. J Pediatr 1996; 128: 313-318.
-
(1996)
J Pediatr
, vol.128
, pp. 313-318
-
-
Massicotte, P.1
Adams, M.2
Marzinotto, V.3
Brooker, L.A.4
Andrew, M.5
-
364
-
-
0001178540
-
Nomogram to establish therapeutic levels Of the lowmolec- ular weight heparin (lmwh), clivarine in children requir- ingtreatmentforvenous thromboembolism (vte)
-
Massicotte, M. P., Adams, M., Leaker, M., Andrew, M. A nomogram to establish therapeutic levels Of the lowmolec- ular weight heparin (LMWH), clivarine in children requir- ingtreatmentforvenous thromboembolism (VTE). Thromb Haemost 1997; (Suppl): 282.
-
(1997)
Thromb Haemost
, pp. 282
-
-
Massicotte, M.P.1
Adams, M.2
Leaker, M.3
Andrew, M.A.4
-
365
-
-
0025758825
-
Report of scientific and standardization subcommittee on neonatal hemostasis: Normal coagulation data for fetuses and newborn infants
-
Hathaway, W., Corrigan, J. Report of Scientific and Standardization Subcommittee on Neonatal Hemostasis: normal coagulation data for fetuses and newborn infants. Thromb Haemost 1991; 65: 323-325.
-
(1991)
Thromb Haemost
, vol.65
, pp. 323-325
-
-
Hathaway, W.1
Corrigan, J.2
-
366
-
-
0028625312
-
Thrombin regulation in children differs from adults in the absence and presence of heparin
-
Andrew, M., Mitchell, L., Vegh, P., Of osu, F. Thrombin regulation in children differs from adults in the absence and presence of heparin. Thromb Haemost 1994; 72: 836-842.
-
(1994)
Thromb Haemost
, vol.72
, pp. 836-842
-
-
Andrew, M.1
Mitchell, L.2
Vegh, P.3
Ofosu, F.4
-
367
-
-
0026541515
-
Report of scientific and standardization subcommittee on neonatal hemostasis diagnosis and treatment of neonatal thrombosis
-
Schmidt, B., Andrew, M. Report of Scientific and Standardization Subcommittee on Neonatal Hemostasis Diagnosis and Treatment of Neonatal Thrombosis. Thromb Haemost 1992; 67: 381-382.
-
(1992)
Thromb Haemost
, vol.67
, pp. 381-382
-
-
Schmidt, B.1
Andrew, M.2
-
368
-
-
0027339052
-
Vitamin k1 metabolism and the production of des-carboxy prothrombin and protein c in the term and premature neonate
-
Bovill, E. G., Soll, R., Lynch, M., etal.Vitamin K1 metabolism and the production of des-carboxy prothrombin and protein C in the term and premature neonate. Blood 1993; 81: 77-83.
-
(1993)
Blood
, vol.81
, pp. 77-83
-
-
Bovill, E.G.1
Soll, R.2
Lynch, M.3
-
369
-
-
0020319935
-
The content of phylloquinone (vitamin k1) in human milk, cow’s milk and infant formula foods determined by high-performance liquid chromatography
-
Haroon, Y., Shearer, M. J., Rahim, S., et al. The content of phylloquinone (vitamin K1) in human milk, cow’s milk and infant formula foods determined by high-performance liquid chromatography. J Nutr 1982; 112:1105-1117.
-
(1982)
J Nutr
, vol.112
, pp. 1105-1117
-
-
Haroon, Y.1
Shearer, M.J.2
Rahim, S.3
-
370
-
-
0023522353
-
Vitamin k1 content of maternal milk: Influence of the stage of lactation, lipid composition, and vitamin k1 supplements given to the mother
-
VonKries, R., Shearer, M. J., McCarthy, P T., etal. Vitamin K1 content of maternal milk: influence of the stage of lactation, lipid composition, and vitamin K1 supplements given to the mother. Pediatr Res 1987; 22: 513-517.
-
(1987)
Pediatr Res
, vol.22
, pp. 513-517
-
-
Vonkries, R.1
Shearer, M.J.2
McCarthy, P.T.3
-
371
-
-
0021889672
-
Warfarin absorption in a patient with short-bowel syndrome
-
Lehman, M., Kolb, K., Barnhart, G. R., Wagman, L., Barr, W. H. Warfarin absorption in a patient with short-bowel syndrome. Clin Pharm 1985; 4: 325-326.
-
(1985)
Clin Pharm
, vol.4
, pp. 325-326
-
-
Lehman, M.1
Kolb, K.2
Barnhart, G.R.3
Wagman, L.4
Barr, W.H.5
-
372
-
-
0024378740
-
Newborn’s fibrinolytic mechanism: Components and plasmin generation
-
Corrigan, J. J., Jr, Sleeth, J. J., Jeter, M., Lox, C. D. Newborn’s fibrinolytic mechanism: components and plasmin generation. Am J Hematol 1989; 32: 273-278.
-
(1989)
Am J Hematol
, vol.32
, pp. 273-278
-
-
Corrigan, J.J.1
Sleeth, J.J.2
Jeter, M.3
Lox, C.D.4
-
373
-
-
0026786155
-
Fibrin clot lysis by thrombolytic agents is impaired in newborns due to a low plasminogen concentration
-
Andrew, M., Brooker, L., Leaker, M., Paes, B., Weitz, J. Fibrin clot lysis by thrombolytic agents is impaired in newborns due to a low plasminogen concentration. Thromb Haemost 1992; 68: 325-330.
-
(1992)
Thromb Haemost
, vol.68
, pp. 325-330
-
-
Andrew, M.1
Brooker, L.2
Leaker, M.3
Paes, B.4
Weitz, J.5
-
374
-
-
0029082893
-
Fibrin clot lysis by tissue plasminogen activator (tpa) is impaired in plasma from pediatric liver transplant patients
-
Leaker, M., Superina, R., Andrew, M. Fibrin clot lysis by tissue plasminogen activator (tPA) is impaired in plasma from pediatric liver transplant patients. Transplantation 1995; 60:144-147.
-
(1995)
Transplantation
, vol.60
, pp. 144-147
-
-
Leaker, M.1
Superina, R.2
Andrew, M.3
-
375
-
-
0030762059
-
Intracerebral hemorrhage during fibrinolytic therapy in children: A review of the literature of the last thirty years
-
Zenz, W., Arlt, F., Sodia, S., Berghold, A. Intracerebral hemorrhage during fibrinolytic therapy in children: a review of the literature of the last thirty years. Semin ThrombosHaemost 1997; 23:321-332.
-
(1997)
Semin Thromboshaemost
, vol.23
, pp. 321-332
-
-
Zenz, W.1
Arlt, F.2
Sodia, S.3
Berghold, A.4
-
376
-
-
0026592652
-
Monitoring thrombolytic therapy
-
Bovill, E. G., Becker, R., Tracy, R. P. Monitoring thrombolytic therapy. Progr Cardiovasc Dis 1992; 34: 279-294.
-
(1992)
Progr Cardiovasc Dis
, vol.34
, pp. 279-294
-
-
Bovill, E.G.1
Becker, R.2
Tracy, R.P.3
-
377
-
-
0029145238
-
Blood component therapy in neonatal hemostatic disorders. [published erratum appears in transfus med rev 1996; 10: 248]
-
Andrew, M., Brooker, L. A. Blood component therapy in neonatal hemostatic disorders. [Published erratum appears in Transfus Med Rev 1996; 10: 248] Transfus Med Rev 1995; 9: 231-250.
-
(1995)
Transfus Med Rev
, vol.9
, pp. 231-250
-
-
Andrew, M.1
Brooker, L.A.2
-
378
-
-
84927951163
-
Antithrombictherapy in children
-
Monagle, P., Chan, A., Massicotte, P., Chalmers, E., Michelson, A. D.Antithrombictherapy in children.Chest 2004;126: 6455-6875.
-
(2004)
Chest
, vol.126
, pp. 6455-6875
-
-
Monagle, P.1
Chan, A.2
Massicotte, P.3
Chalmers, E.4
Michelson, A.D.5
-
379
-
-
0031761176
-
Antithrombotic therapy in children
-
Michelson, A. D., Bovill, E., Monagle, P., Andrew, M. Antithrombotic therapy in children. Chest 1998; 114:748S-769S.
-
(1998)
Chest
, vol.114
, pp. 748S-769S
-
-
Michelson, A.D.1
Bovill, E.2
Monagle, P.3
Andrew, M.4
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