-
1
-
-
33144490691
-
Grading strength of recommendations and quality of evidence in clinical guidelines: report from an American college of chest physicians task force
-
Guyatt G, Gutterman D, Baumann MH. Grading strength of recommendations and quality of evidence in clinical guidelines: report from an American college of chest physicians task force. Chest 2006, 129:174-81.
-
(2006)
Chest
, vol.129
, pp. 174-181
-
-
Guyatt, G.1
Gutterman, D.2
Baumann, M.H.3
-
2
-
-
0025917404
-
Pregnancy in congenital afibrinogenaemia: report of a successful case and review of the literature
-
Grech H, Majumdar G, Lawrie AS, Savidge GF. Pregnancy in congenital afibrinogenaemia: report of a successful case and review of the literature. Br J Haematol 1991, 78:571-2.
-
(1991)
Br J Haematol
, vol.78
, pp. 571-572
-
-
Grech, H.1
Majumdar, G.2
Lawrie, A.S.3
Savidge, G.F.4
-
3
-
-
0343603909
-
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia
-
Lak M, Keihani M, Elahi F, Peyvandi F, Mannucci PM. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia. Br J Haematol 1999, 107:204-6.
-
(1999)
Br J Haematol
, vol.107
, pp. 204-206
-
-
Lak, M.1
Keihani, M.2
Elahi, F.3
Peyvandi, F.4
Mannucci, P.M.5
-
4
-
-
0024533298
-
Congenital hypofibrinogenemia in pregnancy
-
Goodwin TM. Congenital hypofibrinogenemia in pregnancy. Obstet Gynecol Surv 1989, 44:157-61.
-
(1989)
Obstet Gynecol Surv
, vol.44
, pp. 157-161
-
-
Goodwin, T.M.1
-
5
-
-
0033828227
-
Hypofibrinogenaemia with compound heterozygosity for two γ chain mutations γ Ala→Gly and an intron two Gt→At splice site mutation
-
Wyatt J, Brennan SO, May S, George PM. Hypofibrinogenaemia with compound heterozygosity for two γ chain mutations γ Ala→Gly and an intron two Gt→At splice site mutation. Thromb Haemost 2000, 84:449-52.
-
(2000)
Thromb Haemost
, vol.84
, pp. 449-452
-
-
Wyatt, J.1
Brennan, S.O.2
May, S.3
George, P.M.4
-
6
-
-
4444364103
-
Rare bleeding disorder registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias
-
Acharya SS, Coughlin A, Dimichele DM. Rare bleeding disorder registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004, 2:248-56.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 248-256
-
-
Acharya, S.S.1
Coughlin, A.2
Dimichele, D.M.3
-
7
-
-
35748977954
-
Fibrinogen Columbus: a novel gamma Gly200Val mutation causing hypofibrinogenemia in a family with associated thrombophilia
-
Davis RL, Mosesson MW, Kerlin BA, Canner JA, Ruymann FB, Brennan SO. Fibrinogen Columbus: a novel gamma Gly200Val mutation causing hypofibrinogenemia in a family with associated thrombophilia. Haematologica 2007, 92:1151-2.
-
(2007)
Haematologica
, vol.92
, pp. 1151-1152
-
-
Davis, R.L.1
Mosesson, M.W.2
Kerlin, B.A.3
Canner, J.A.4
Ruymann, F.B.5
Brennan, S.O.6
-
8
-
-
33744471907
-
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bb-chain gene
-
Monaldini L, Asselta R, Duga S. Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bb-chain gene. Haematologica 2006, 91:628-33.
-
(2006)
Haematologica
, vol.91
, pp. 628-633
-
-
Monaldini, L.1
Asselta, R.2
Duga, S.3
-
9
-
-
32344436263
-
Middle cerebral arterial thrombosis in a patient with hypofibrinogenemia, 5 days after rFVIIa and FFP infusion
-
Patiroglu T, Karakukcu M. Middle cerebral arterial thrombosis in a patient with hypofibrinogenemia, 5 days after rFVIIa and FFP infusion. Clin Appl Thromb Hemost 2006, 12:111-3.
-
(2006)
Clin Appl Thromb Hemost
, vol.12
, pp. 111-113
-
-
Patiroglu, T.1
Karakukcu, M.2
-
10
-
-
0027090235
-
Severe congenital dysfibrinogenemia (fibrinogen-Riyadh): a family study
-
al-Fawaz IM, Gader AM. Severe congenital dysfibrinogenemia (fibrinogen-Riyadh): a family study. Acta Haematol 1992, 88:194-7.
-
(1992)
Acta Haematol
, vol.88
, pp. 194-197
-
-
al-Fawaz, I.M.1
Gader, A.M.2
-
11
-
-
0034975060
-
A database for human fibrinogen variants
-
Hanss M, Biot F. A database for human fibrinogen variants. Ann NY Acad Sci 2001, 936:89-90. http://www.geht.org/databaseang/fibrinogen
-
(2001)
Ann NY Acad Sci
, vol.936
, pp. 89-90
-
-
Hanss, M.1
Biot, F.2
-
13
-
-
0033673952
-
Spontaneous intracranial bleeding in two patients with congenital afibrinogenaemia and the role of replacement therapy
-
Parameswaran R, Dickinson JP, De Lord S, Keeling DM, Colvin BT. Spontaneous intracranial bleeding in two patients with congenital afibrinogenaemia and the role of replacement therapy. Haemophilia 2000, 6:705-8.
-
(2000)
Haemophilia
, vol.6
, pp. 705-708
-
-
Parameswaran, R.1
Dickinson, J.P.2
De Lord, S.3
Keeling, D.M.4
Colvin, B.T.5
-
14
-
-
0018887670
-
Congenital afibrinogenemia in 10 offsprings of uncle-niece marriage
-
Fried K, Kaufman S. Congenital afibrinogenemia in 10 offsprings of uncle-niece marriage. Clin Genet 1980, 17:223-7.
-
(1980)
Clin Genet
, vol.17
, pp. 223-227
-
-
Fried, K.1
Kaufman, S.2
-
15
-
-
3042690801
-
Pregnancy-related thrombosis in a woman with congenital afibrinogenemia: a report of two successful pregnancies
-
Roque H, Stephenson C, Lee MJ. Pregnancy-related thrombosis in a woman with congenital afibrinogenemia: a report of two successful pregnancies. Am J Hematol 2004, 76:267-70.
-
(2004)
Am J Hematol
, vol.76
, pp. 267-270
-
-
Roque, H.1
Stephenson, C.2
Lee, M.J.3
-
16
-
-
34147174335
-
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusions
-
Aygoren-Pursun E, Martinez Saguer I, Rusicke E. Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusions. Am J Haematol 2007, 82:317-20.
-
(2007)
Am J Haematol
, vol.82
, pp. 317-320
-
-
Aygoren-Pursun, E.1
Martinez Saguer, I.2
Rusicke, E.3
-
18
-
-
20444408784
-
Efficacy and tolerability of a pasteurised human fibrinogen concentrate in patients with congenital fibrinogen deficiency
-
Kreuz W, Meili E, Peter-Salonen K. Efficacy and tolerability of a pasteurised human fibrinogen concentrate in patients with congenital fibrinogen deficiency. Trans Apher Sci 2005, 32:247-53.
-
(2005)
Trans Apher Sci
, vol.32
, pp. 247-253
-
-
Kreuz, W.1
Meili, E.2
Peter-Salonen, K.3
-
19
-
-
0031743980
-
Congenital deficiencies and abnormalities of prothrombin
-
Girolami A, Scarano L, Saggiorato G, Girolami B, Bertomoro A, Marchiori A. Congenital deficiencies and abnormalities of prothrombin. Blood Coagul Fibrinolysis 1998, 9:557-69.
-
(1998)
Blood Coagul Fibrinolysis
, vol.9
, pp. 557-569
-
-
Girolami, A.1
Scarano, L.2
Saggiorato, G.3
Girolami, B.4
Bertomoro, A.5
Marchiori, A.6
-
20
-
-
0033382096
-
Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy
-
Strijks E, Poort SR, Renier WO, Gabreels FJ, Bertina RM. Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy. Neuropediatrics 1999, 30:320-4.
-
(1999)
Neuropediatrics
, vol.30
, pp. 320-324
-
-
Strijks, E.1
Poort, S.R.2
Renier, W.O.3
Gabreels, F.J.4
Bertina, R.M.5
-
21
-
-
33750996176
-
Severe prothrombin deficiency caused by prothrombin-Edmonton (R-4Q) combined with a previously undetected deletion
-
Wong AYK, Hewitt J, Clarke BJ. Severe prothrombin deficiency caused by prothrombin-Edmonton (R-4Q) combined with a previously undetected deletion. J Thromb Haemost 2006, 4:2623-8.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2623-2628
-
-
Wong, A.Y.K.1
Hewitt, J.2
Clarke, B.J.3
-
22
-
-
0028650365
-
Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorder
-
Poort SR, Michiels JJ, Reitsma PH, Bertina RM. Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorder. Thromb Haemost 1994, 72:819-24.
-
(1994)
Thromb Haemost
, vol.72
, pp. 819-824
-
-
Poort, S.R.1
Michiels, J.J.2
Reitsma, P.H.3
Bertina, R.M.4
-
23
-
-
0033981470
-
The prothrombin Denver patient has two different prothrombin point mutations resulting in Glu-300→Lys and Glu-309→Lys substitutions
-
Lefkowitz JB, Haver T, Clarke S, Jacobson L, Weller A, Nuss R. The prothrombin Denver patient has two different prothrombin point mutations resulting in Glu-300→Lys and Glu-309→Lys substitutions. Br J Haematol 2000, 108:182-7.
-
(2000)
Br J Haematol
, vol.108
, pp. 182-187
-
-
Lefkowitz, J.B.1
Haver, T.2
Clarke, S.3
Jacobson, L.4
Weller, A.5
Nuss, R.6
-
25
-
-
3843121109
-
Successful prophylactic treatment for bleeding in a girl with severe hereditary prothrombin deficiency using a prothrombin complex concentrate (Bebulin® VH)
-
Lobel JS, Majumdar S, Kovats-Bell S. Successful prophylactic treatment for bleeding in a girl with severe hereditary prothrombin deficiency using a prothrombin complex concentrate (Bebulin® VH). J Pediatr Hematol Oncol 2004, 26:480-3.
-
(2004)
J Pediatr Hematol Oncol
, vol.26
, pp. 480-483
-
-
Lobel, J.S.1
Majumdar, S.2
Kovats-Bell, S.3
-
26
-
-
0017925840
-
Prothrombin quick. A newly identified dysprothrombinaemia
-
Owen CA, Henriksen RA, McDuffie FC, Mann KG. Prothrombin quick. A newly identified dysprothrombinaemia. Mayo Clin Proc 1978, 53:29-33.
-
(1978)
Mayo Clin Proc
, vol.53
, pp. 29-33
-
-
Owen, C.A.1
Henriksen, R.A.2
McDuffie, F.C.3
Mann, K.G.4
-
27
-
-
0025146359
-
Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulants
-
Brenner B, Tavori S, Zivelin A. Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulants. Br J Haematol 1990, 222:537-42.
-
(1990)
Br J Haematol
, vol.222
, pp. 537-542
-
-
Brenner, B.1
Tavori, S.2
Zivelin, A.3
-
28
-
-
29144531829
-
Congenital vitamin K-dependent coagulation factor deficiency: a case report
-
Bhattacharyya J, Dutta P, Mishra P. Congenital vitamin K-dependent coagulation factor deficiency: a case report. Blood Coagul Fibrinolysis 2005, 16:525-7.
-
(2005)
Blood Coagul Fibrinolysis
, vol.16
, pp. 525-527
-
-
Bhattacharyya, J.1
Dutta, P.2
Mishra, P.3
-
29
-
-
0034530536
-
Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex
-
Oldenburg J, von Brederlow B, Fregin A. Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex. Thromb Haemost 2000, 84:937-41.
-
(2000)
Thromb Haemost
, vol.84
, pp. 937-941
-
-
Oldenburg, J.1
von Brederlow, B.2
Fregin, A.3
-
30
-
-
0035052205
-
Combined deficiency of factors II, VII, IX and X (Borgshulte-Grigsby Deficiency) in pregnancy
-
McMahon MJ, James AH. Combined deficiency of factors II, VII, IX and X (Borgshulte-Grigsby Deficiency) in pregnancy. Obstet gynaecol 2001, 97:808-9.
-
(2001)
Obstet gynaecol
, vol.97
, pp. 808-809
-
-
McMahon, M.J.1
James, A.H.2
-
31
-
-
0032535284
-
A missense mutation in γ-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factors
-
Brenner B, Sánchez-Vega B, Wu SM, Lanir N, Stafford DW, Solera J. A missense mutation in γ-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factors. Blood 1998, 92:4554-9.
-
(1998)
Blood
, vol.92
, pp. 4554-4559
-
-
Brenner, B.1
Sánchez-Vega, B.2
Wu, S.M.3
Lanir, N.4
Stafford, D.W.5
Solera, J.6
-
32
-
-
0014009563
-
Congenital combined deficiency of coagulation factors II, VII, IX and X: report of a case
-
McMillan CW, Roberts HR. Congenital combined deficiency of coagulation factors II, VII, IX and X: report of a case. N Engl J Med 1966, 274:1313-5.
-
(1966)
N Engl J Med
, vol.274
, pp. 1313-1315
-
-
McMillan, C.W.1
Roberts, H.R.2
-
33
-
-
0032860559
-
Use of prothrombin complex concentrates for prophylaxis and treatment of bleeding episodes in patients with hereditary deficiency of prothrombin, factor VII, factor X, Protein C, Protein S, or protein Z
-
Lechler E. Use of prothrombin complex concentrates for prophylaxis and treatment of bleeding episodes in patients with hereditary deficiency of prothrombin, factor VII, factor X, Protein C, Protein S, or protein Z. Thromb Res 1999, 95:S39-50.
-
(1999)
Thromb Res
, vol.95
-
-
Lechler, E.1
-
34
-
-
0035003643
-
Factor V inhibitor in neonatal intracranial hemorrhage secondary to severe congenital factor V deficiency
-
Lee WS, Chong LA, Begum S, Abdullah WA, Koh MT, Lim EJ. Factor V inhibitor in neonatal intracranial hemorrhage secondary to severe congenital factor V deficiency. J Pediatr Hematol Oncol 2001, 23:244-6.
-
(2001)
J Pediatr Hematol Oncol
, vol.23
, pp. 244-246
-
-
Lee, W.S.1
Chong, L.A.2
Begum, S.3
Abdullah, W.A.4
Koh, M.T.5
Lim, E.J.6
-
35
-
-
0033996029
-
Severe factor V deficiency and neonatal intracranial haemorrhage: a case report
-
Salooja N, Martin P, Khair K, Liesner R, Hann I. Severe factor V deficiency and neonatal intracranial haemorrhage: a case report. Haemophilia 2000, 6:44-6.
-
(2000)
Haemophilia
, vol.6
, pp. 44-46
-
-
Salooja, N.1
Martin, P.2
Khair, K.3
Liesner, R.4
Hann, I.5
-
36
-
-
0033041974
-
Intracranial haemorrhage due to factor V deficiency
-
Totan M, Albayrak D. Intracranial haemorrhage due to factor V deficiency. Acta Paediatr 1999, 88:342-3.
-
(1999)
Acta Paediatr
, vol.88
, pp. 342-343
-
-
Totan, M.1
Albayrak, D.2
-
37
-
-
0021180472
-
Factor V deficiency and antenatal intraventricular haemorrhage
-
Whitelaw A, Haines ME, Bolsover W, Harris E. Factor V deficiency and antenatal intraventricular haemorrhage. Arch Dis Child 1984, 59:997-9.
-
(1984)
Arch Dis Child
, vol.59
, pp. 997-999
-
-
Whitelaw, A.1
Haines, M.E.2
Bolsover, W.3
Harris, E.4
-
38
-
-
0026587475
-
Familial intracranial haemorrhage due to factor V deficiency
-
Wadia RS, Sangle SA, Kripalaney S, Bafna M, Karva SR. Familial intracranial haemorrhage due to factor V deficiency. J Neurol Neurosurg Psychiatry 1992, 55:227-8.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 227-228
-
-
Wadia, R.S.1
Sangle, S.A.2
Kripalaney, S.3
Bafna, M.4
Karva, S.R.5
-
39
-
-
16344365612
-
The use of activated recombinant coagulation factor VII during haemarthroses and synovectomy in a patient with congenital severe factor V deficiency
-
Gonzalez-Boullosa R, Ocampo-Martinez R, Alarcon-Martin MJ, Suarez-Rodriguez M, Dominguez-Viguera L, Gonzalez-Fajo G. The use of activated recombinant coagulation factor VII during haemarthroses and synovectomy in a patient with congenital severe factor V deficiency. Haemophilia 2005, 11:167-70.
-
(2005)
Haemophilia
, vol.11
, pp. 167-170
-
-
Gonzalez-Boullosa, R.1
Ocampo-Martinez, R.2
Alarcon-Martin, M.J.3
Suarez-Rodriguez, M.4
Dominguez-Viguera, L.5
Gonzalez-Fajo, G.6
-
40
-
-
16344385867
-
Severe congenital factor V deficiency: successful treatment with recombinant factor VIIa in two brothers
-
abstract no. 3876
-
Borel-Derlon A, Slaoui M, Le Querrec A, Hugel B, Vos HL. Severe congenital factor V deficiency: successful treatment with recombinant factor VIIa in two brothers. Blood 2002, 100. abstract no. 3876
-
(2002)
Blood
, vol.100
-
-
Borel-Derlon, A.1
Slaoui, M.2
Le Querrec, A.3
Hugel, B.4
Vos, H.L.5
-
42
-
-
0020322169
-
Combined factor V and factor VIII deficiency among non-Ashkenazi Jews
-
Seligsohn U, Zivelin A, Zwang E. Combined factor V and factor VIII deficiency among non-Ashkenazi Jews. N Engl J Med 1982, 307:1191-5.
-
(1982)
N Engl J Med
, vol.307
, pp. 1191-1195
-
-
Seligsohn, U.1
Zivelin, A.2
Zwang, E.3
-
43
-
-
0031881892
-
Bleeding symptoms in Iranian patients with the combined deficiency of factor V and factor VIII
-
Peyvandi F, Tuddenham EGD, Akhtari AM, Lak M, Mannucci PM. Bleeding symptoms in Iranian patients with the combined deficiency of factor V and factor VIII. Br J Haematol 1998, 100:773-6.
-
(1998)
Br J Haematol
, vol.100
, pp. 773-776
-
-
Peyvandi, F.1
Tuddenham, E.G.D.2
Akhtari, A.M.3
Lak, M.4
Mannucci, P.M.5
-
44
-
-
1642369785
-
Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family
-
Faioni EM, Fontana G, Carpani G. Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family. Thromb Res 2003, 112:269-71.
-
(2003)
Thromb Res
, vol.112
, pp. 269-271
-
-
Faioni, E.M.1
Fontana, G.2
Carpani, G.3
-
45
-
-
0026229088
-
Management of cesarean section under replacement therapy with factor VIII concentrates in a pregnant case with congenital combined deficiency of factor V and factor VIII
-
Ueno H, Asami M, Yoneda R. Management of cesarean section under replacement therapy with factor VIII concentrates in a pregnant case with congenital combined deficiency of factor V and factor VIII. Rinsho Ketsueki 1991, 32:981-5.
-
(1991)
Rinsho Ketsueki
, vol.32
, pp. 981-985
-
-
Ueno, H.1
Asami, M.2
Yoneda, R.3
-
46
-
-
0028402373
-
Combined factor V and factor VIII deficiency with congenital heart disease: response to plasma and DDAVP infusion
-
Chuansumrit A, Mahaphan W, Pintadit P. Combined factor V and factor VIII deficiency with congenital heart disease: response to plasma and DDAVP infusion. Southeast Asian J Trop Med Public Health 1994, 25:217-20.
-
(1994)
Southeast Asian J Trop Med Public Health
, vol.25
, pp. 217-220
-
-
Chuansumrit, A.1
Mahaphan, W.2
Pintadit, P.3
-
47
-
-
19544380905
-
Successful use of fresh frozen plasma and desmopressin for transurethral prostatectomy in a french basque with combined factors V + VIII deficiency
-
Bauduer F, Guichandut JP, Ducout L. Successful use of fresh frozen plasma and desmopressin for transurethral prostatectomy in a french basque with combined factors V + VIII deficiency. J Thromb Haemost 2004, 2:675-6.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 675-676
-
-
Bauduer, F.1
Guichandut, J.P.2
Ducout, L.3
-
48
-
-
0037298358
-
Two novel cases of cerebral haemorrhages at the neonatal period associated with inherited factor VII deficiency, one of them revealing a new nonsense mutation (Ser52Stop)
-
Giansily-Blaizot M, Aguilar-Martinez P, Briquel ME. Two novel cases of cerebral haemorrhages at the neonatal period associated with inherited factor VII deficiency, one of them revealing a new nonsense mutation (Ser52Stop). Blood Coagul Fibrinolysis 2003, 14:217-20.
-
(2003)
Blood Coagul Fibrinolysis
, vol.14
, pp. 217-220
-
-
Giansily-Blaizot, M.1
Aguilar-Martinez, P.2
Briquel, M.E.3
-
49
-
-
4444364103
-
Rare bleeding disorder tegistry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias
-
Acharya SS, Coughlin A, Dimichele DM. Rare bleeding disorder tegistry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004, 2:248-56.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 248-256
-
-
Acharya, S.S.1
Coughlin, A.2
Dimichele, D.M.3
-
50
-
-
0030669247
-
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency
-
Peyvandi F, Mannucci PM, Asti D, Abdoullahi M, Di Rocco N, Sharifian R. Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency. Haemophilia 1997, 3:242-6.
-
(1997)
Haemophilia
, vol.3
, pp. 242-246
-
-
Peyvandi, F.1
Mannucci, P.M.2
Asti, D.3
Abdoullahi, M.4
Di Rocco, N.5
Sharifian, R.6
-
51
-
-
39049193204
-
Pregnancy in women with congenital factor VII deficiency
-
Kulkarni AA, Lee CA, Kadir RA. Pregnancy in women with congenital factor VII deficiency. Haemophilia 2006, 12:413-6.
-
(2006)
Haemophilia
, vol.12
, pp. 413-416
-
-
Kulkarni, A.A.1
Lee, C.A.2
Kadir, R.A.3
-
52
-
-
0021255636
-
Hereditary factor VII deficiency: report of a case of intracranial hemorrhage
-
Hassan HJ, Casalbore P, De Laurenzi A, Petti N, Sinibaldi L, Orlando M. Hereditary factor VII deficiency: report of a case of intracranial hemorrhage. Haemostasis 1984, 14:244-8.
-
(1984)
Haemostasis
, vol.14
, pp. 244-248
-
-
Hassan, H.J.1
Casalbore, P.2
De Laurenzi, A.3
Petti, N.4
Sinibaldi, L.5
Orlando, M.6
-
53
-
-
0019465270
-
Factor VII deficiency
-
Ragni MV, Lewis JH, Spero JA, Hasiba U. Factor VII deficiency. Am J Hematol 1981, 10:79-88.
-
(1981)
Am J Hematol
, vol.10
, pp. 79-88
-
-
Ragni, M.V.1
Lewis, J.H.2
Spero, J.A.3
Hasiba, U.4
-
54
-
-
33645982863
-
Disorders of menstruation and their effect on the quality of life in women with congenital factor VII deficiency
-
Kulkarni A, Lee CA, Griffeon A, Kadir RA. Disorders of menstruation and their effect on the quality of life in women with congenital factor VII deficiency. Haemophilia 2006, 12:248-52.
-
(2006)
Haemophilia
, vol.12
, pp. 248-252
-
-
Kulkarni, A.1
Lee, C.A.2
Griffeon, A.3
Kadir, R.A.4
-
55
-
-
63049094038
-
Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene
-
Herrmann FH, Wulff K, Auerswald G. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene. Haemophilia 2009, 15:267-80.
-
(2009)
Haemophilia
, vol.15
, pp. 267-280
-
-
Herrmann, F.H.1
Wulff, K.2
Auerswald, G.3
-
56
-
-
27844481104
-
Potential predictors of bleeding risk in inherited factor VII deficiency clinical, biological and molecular criteria
-
Giansily-Blaizot M, Schved JF. Potential predictors of bleeding risk in inherited factor VII deficiency clinical, biological and molecular criteria. Thromb Haemost 2005, 94:901-6.
-
(2005)
Thromb Haemost
, vol.94
, pp. 901-906
-
-
Giansily-Blaizot, M.1
Schved, J.F.2
-
57
-
-
0036881437
-
Outcome of intracranial hemorrhage in infants with congenital factor VII deficiency
-
Chuansumrit A, Visanuyothin N, Puapunwattana S. Outcome of intracranial hemorrhage in infants with congenital factor VII deficiency. J Med Assoc Thai 2002, 85(Suppl 4):S1059-64.
-
(2002)
J Med Assoc Thai
, vol.85
, Issue.SUPPL 4
-
-
Chuansumrit, A.1
Visanuyothin, N.2
Puapunwattana, S.3
-
58
-
-
11044234346
-
Clinical picture and management of congenital factor VII deficiency
-
Mariani G, Dolce A, Marchetti G, Bernardi F. Clinical picture and management of congenital factor VII deficiency. Haemophilia 2004, 10(Suppl. 4):180-3.
-
(2004)
Haemophilia
, vol.10
, Issue.SUPPL. 4
, pp. 180-183
-
-
Mariani, G.1
Dolce, A.2
Marchetti, G.3
Bernardi, F.4
-
59
-
-
0029865789
-
Treatment of factor VII deficiency with recombinant factor VIIa
-
Bauer KA. Treatment of factor VII deficiency with recombinant factor VIIa. Haemostasis 1996, 26:155-8.
-
(1996)
Haemostasis
, vol.26
, pp. 155-158
-
-
Bauer, K.A.1
-
60
-
-
19944408221
-
Hepatocyte transplantation for inherited factor VII deficiency
-
Dhawan A, Mitry RR, Hughes RD. Hepatocyte transplantation for inherited factor VII deficiency. Transplantation 2004, 78:1812-4.
-
(2004)
Transplantation
, vol.78
, pp. 1812-1814
-
-
Dhawan, A.1
Mitry, R.R.2
Hughes, R.D.3
-
61
-
-
44649186151
-
Successful control of central nervous system bleeding in two newborns with severe factor VII deficiency using rFVIIa administered via Port-a-Cath
-
Karimi M. Successful control of central nervous system bleeding in two newborns with severe factor VII deficiency using rFVIIa administered via Port-a-Cath. Semin Hematol 2008, 45(2 Suppl 1):S74.
-
(2008)
Semin Hematol
, vol.45
, Issue.2 SUPPL 1
-
-
Karimi, M.1
-
62
-
-
0034570627
-
Successful prophylaxis of intracranial hemorrhage in infants with severe congenital factor VII deficiency
-
Kankirawatana S, Mahasandana C, Veerakul G. Successful prophylaxis of intracranial hemorrhage in infants with severe congenital factor VII deficiency. Southeast Asian J Trop Med Public Health 2000, 31:795-800.
-
(2000)
Southeast Asian J Trop Med Public Health
, vol.31
, pp. 795-800
-
-
Kankirawatana, S.1
Mahasandana, C.2
Veerakul, G.3
-
63
-
-
35048820395
-
Recombinant factor VIIa for long-term replacement therapy in patients with congenital factor VII deficiency
-
Huth-Kühne A, Rott H, Zimmermann R, Halimeh S. Recombinant factor VIIa for long-term replacement therapy in patients with congenital factor VII deficiency. Thromb Haemost 2007, 10:912-5.
-
(2007)
Thromb Haemost
, vol.10
, pp. 912-915
-
-
Huth-Kühne, A.1
Rott, H.2
Zimmermann, R.3
Halimeh, S.4
-
64
-
-
33846413238
-
Successful prophylaxis against intracranial hemorrhage using weekly administration of activated recombinant factor VII in a newborn with severe factor VII deficiency
-
Farah RA, Hamod D, Melick N, Giansily-Blaizot M, Sallah S. Successful prophylaxis against intracranial hemorrhage using weekly administration of activated recombinant factor VII in a newborn with severe factor VII deficiency. J Thromb Haemost 2007, 5:433-4.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 433-434
-
-
Farah, R.A.1
Hamod, D.2
Melick, N.3
Giansily-Blaizot, M.4
Sallah, S.5
-
66
-
-
31644439475
-
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4 + 1G→A
-
Hennewig U, Eisert S, Wulff K, Herrmann FH, Schneider DT, Göbel U. Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4 + 1G→A. Pediatr Hematol Oncol 2006, 23:129-33.
-
(2006)
Pediatr Hematol Oncol
, vol.23
, pp. 129-133
-
-
Hennewig, U.1
Eisert, S.2
Wulff, K.3
Herrmann, F.H.4
Schneider, D.T.5
Göbel, U.6
-
67
-
-
3142739015
-
Prophylactic effect of recombinant factor VIIa in factor VII deficient patients
-
Mathijssen NC, Masereeuw R, Verbeek K, Lavergne JM, Costa JM, van Heerde WL. Prophylactic effect of recombinant factor VIIa in factor VII deficient patients. Br J Haematol 2004, 125:494-9.
-
(2004)
Br J Haematol
, vol.125
, pp. 494-499
-
-
Mathijssen, N.C.1
Masereeuw, R.2
Verbeek, K.3
Lavergne, J.M.4
Costa, J.M.5
van Heerde, W.L.6
-
68
-
-
2342649465
-
Recombinant factor VIIa prophylaxis in a patient with severe congenital factor VII deficiency
-
Tcheng WY, Donkin J, Konzal S, Wong WY. Recombinant factor VIIa prophylaxis in a patient with severe congenital factor VII deficiency. Haemophilia 2004, 10:295-8.
-
(2004)
Haemophilia
, vol.10
, pp. 295-298
-
-
Tcheng, W.Y.1
Donkin, J.2
Konzal, S.3
Wong, W.Y.4
-
69
-
-
0029560352
-
Prophylaxis and therapy with factor VII concentrate (human) immuno, vapor heated in patients with congenital factor VII deficiency: a summary of case reports
-
Cohen LJ, McWilliams NB, Neuberg R. Prophylaxis and therapy with factor VII concentrate (human) immuno, vapor heated in patients with congenital factor VII deficiency: a summary of case reports. Am J Hematol 1995, 50:269-76.
-
(1995)
Am J Hematol
, vol.50
, pp. 269-276
-
-
Cohen, L.J.1
McWilliams, N.B.2
Neuberg, R.3
-
70
-
-
35148880650
-
Prophylactic treatment of a small child with severe factor VII deficiency using repeat dosing from a single vial of recombinant activated factor VII
-
Michaels LA, Philipp CS, Eisele J, Pappas H, Saidi P. Prophylactic treatment of a small child with severe factor VII deficiency using repeat dosing from a single vial of recombinant activated factor VII. Pediatr Blood Cancer 2007, 49:736-9.
-
(2007)
Pediatr Blood Cancer
, vol.49
, pp. 736-739
-
-
Michaels, L.A.1
Philipp, C.S.2
Eisele, J.3
Pappas, H.4
Saidi, P.5
-
71
-
-
0033824913
-
Continuous infusion of recombinant activated factor VII during caesarean section delivery in a patient with congenital factor VII deficiency
-
Jimenez-Yuste V, Villar A, Morado M. Continuous infusion of recombinant activated factor VII during caesarean section delivery in a patient with congenital factor VII deficiency. Haemophilia 2000, 6:588-90.
-
(2000)
Haemophilia
, vol.6
, pp. 588-590
-
-
Jimenez-Yuste, V.1
Villar, A.2
Morado, M.3
-
72
-
-
0031803370
-
The use of recombinant activated factor VII in congenital and acquired factor VII deficiencies
-
Muleo G, Santoro R, Iannaccaro PG, Papaleo P, Leo F. The use of recombinant activated factor VII in congenital and acquired factor VII deficiencies. Blood Coagul Fibrinol 1998, 9:389-90.
-
(1998)
Blood Coagul Fibrinol
, vol.9
, pp. 389-390
-
-
Muleo, G.1
Santoro, R.2
Iannaccaro, P.G.3
Papaleo, P.4
Leo, F.5
-
73
-
-
0036588699
-
Rare coagulation deficiencies
-
Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia 2002, 8:308-21.
-
(2002)
Haemophilia
, vol.8
, pp. 308-321
-
-
Peyvandi, F.1
Duga, S.2
Akhavan, S.3
Mannucci, P.M.4
-
74
-
-
0021989851
-
Replacement therapy for congenital factor X deficiency
-
Knight RD, Barr CF, Alving BM. Replacement therapy for congenital factor X deficiency. Transfusion 1985, 25:78-80.
-
(1985)
Transfusion
, vol.25
, pp. 78-80
-
-
Knight, R.D.1
Barr, C.F.2
Alving, B.M.3
-
75
-
-
0031848372
-
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients
-
Peyvandi F, Mannucci PM, Lak M. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients. Brit J Haematol 1998, 102:626-8.
-
(1998)
Brit J Haematol
, vol.102
, pp. 626-628
-
-
Peyvandi, F.1
Mannucci, P.M.2
Lak, M.3
-
76
-
-
33747168208
-
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor X gen
-
Herrmann FH, Auerswald G, Ruiz-Saez A. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor X gen. Haemophilia 2006, 12:479-89.
-
(2006)
Haemophilia
, vol.12
, pp. 479-489
-
-
Herrmann, F.H.1
Auerswald, G.2
Ruiz-Saez, A.3
-
77
-
-
0022638498
-
Severe congenital factor X deficiency with intracranial haemorrhage
-
Sumer T, Ahmad M, Sumer NK, Al Mouzan MI. Severe congenital factor X deficiency with intracranial haemorrhage. Eur J Pediatr 1986, 145:119-20.
-
(1986)
Eur J Pediatr
, vol.145
, pp. 119-120
-
-
Sumer, T.1
Ahmad, M.2
Sumer, N.K.3
Al Mouzan, M.I.4
-
78
-
-
0034809391
-
Danazol therapy in factor X deficiency
-
Mukhopadhyay S, Saxena R, Kashyap R, Choudhry VP. Danazol therapy in factor X deficiency. Haemophilia 2001, 7:504-6.
-
(2001)
Haemophilia
, vol.7
, pp. 504-506
-
-
Mukhopadhyay, S.1
Saxena, R.2
Kashyap, R.3
Choudhry, V.P.4
-
79
-
-
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, 63:1168-74.
-
(1988)
Arch Dis Child
, vol.63
, pp. 1168-1174
-
-
De, S.C.1
Clark, T.2
Bradshaw, A.3
-
80
-
-
0035077839
-
Prophylactic treatment of severe factor X deficiency with prothrombin complex concentrate
-
Kouides PA, Kulzer L. Prophylactic treatment of severe factor X deficiency with prothrombin complex concentrate. Haemophilia 2001, 7:220-3.
-
(2001)
Haemophilia
, vol.7
, pp. 220-223
-
-
Kouides, P.A.1
Kulzer, L.2
-
82
-
-
0018938377
-
Factor X deficiency in the neonatal period
-
Machin SJ, Winter MR, Davies SC, Mackie IJ. Factor X deficiency in the neonatal period. Arch Dis Child 1980, 55:406-8.
-
(1980)
Arch Dis Child
, vol.55
, pp. 406-408
-
-
Machin, S.J.1
Winter, M.R.2
Davies, S.C.3
Mackie, I.J.4
-
83
-
-
0036434925
-
The role of primary prophylactic factor replacement therapy in children with severe factor X deficiency
-
McMahon C, Smith J, Goonan C, Byrne M, Smith OP. The role of primary prophylactic factor replacement therapy in children with severe factor X deficiency. Br J Haematol 2002, 119:789-91.
-
(2002)
Br J Haematol
, vol.119
, pp. 789-791
-
-
McMahon, C.1
Smith, J.2
Goonan, C.3
Byrne, M.4
Smith, O.P.5
-
84
-
-
0034535616
-
Letter to the editor: Factor X deficiency: an unusual cause of spontaneous intracranial bleeding
-
Menon NS. Letter to the editor: Factor X deficiency: an unusual cause of spontaneous intracranial bleeding. Indian Pediatr 2000, 37:1390.
-
(2000)
Indian Pediatr
, vol.37
, pp. 1390
-
-
Menon, N.S.1
-
85
-
-
0034201681
-
Factor X deficiency: an unusual cause for spontaneous intracranial bleeding
-
Ramdas J, Ode D, Warrier RP. Factor X deficiency: an unusual cause for spontaneous intracranial bleeding. Indian Pediatr 2000, 37:656-9.
-
(2000)
Indian Pediatr
, vol.37
, pp. 656-659
-
-
Ramdas, J.1
Ode, D.2
Warrier, R.P.3
-
86
-
-
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, 14:163-5.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 163-165
-
-
Sandler, E.1
Gross, S.2
-
87
-
-
33750710455
-
Severe factor X deficiency due to a homozygous mutation Cys364Arg that disrupts a disulphide bond in the catalytic domain
-
Todd T, Perry DJ, Hayman E, Lawrence K, Gattens M, Baglin T. Severe factor X deficiency due to a homozygous mutation Cys364Arg that disrupts a disulphide bond in the catalytic domain. Haemophilia 2006, 12:1-4.
-
(2006)
Haemophilia
, vol.12
, pp. 1-4
-
-
Todd, T.1
Perry, D.J.2
Hayman, E.3
Lawrence, K.4
Gattens, M.5
Baglin, T.6
-
88
-
-
0028899613
-
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews
-
Shpilberg O, Peretz H, Zivelin A. One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews. Blood 1995, 85:429-32.
-
(1995)
Blood
, vol.85
, pp. 429-432
-
-
Shpilberg, O.1
Peretz, H.2
Zivelin, A.3
-
89
-
-
0023731215
-
Inheritance and bleeding in factor XI deficiency
-
Bolton-Maggs PH, Young Wan-Yin B, McCraw AH, Slack J, Kernoff PB. Inheritance and bleeding in factor XI deficiency. Br J Haematol 1988, 69:521-8.
-
(1988)
Br J Haematol
, vol.69
, pp. 521-528
-
-
Bolton-Maggs, P.H.1
Young Wan-Yin, B.2
McCraw, A.H.3
Slack, J.4
Kernoff, P.B.5
-
90
-
-
0027977953
-
Thrombogenic potential of factor XI concentrate
-
Bolton-Maggs PH, Colvin BT, Satchi BT, Lee CA, Lucas GS. Thrombogenic potential of factor XI concentrate. Lancet 1994, 344:748-9.
-
(1994)
Lancet
, vol.344
, pp. 748-749
-
-
Bolton-Maggs, P.H.1
Colvin, B.T.2
Satchi, B.T.3
Lee, C.A.4
Lucas, G.S.5
-
91
-
-
0028122941
-
Activation of the coagulation cascade after infusion of a factor XI concentrate in congenitally deficient patients
-
Mannucci PM, Bauer KA, Santagostino E. Activation of the coagulation cascade after infusion of a factor XI concentrate in congenitally deficient patients. Blood 1994, 84:1314-9.
-
(1994)
Blood
, vol.84
, pp. 1314-1319
-
-
Mannucci, P.M.1
Bauer, K.A.2
Santagostino, E.3
-
92
-
-
47649083020
-
Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency
-
O'Connell NM, Riddell AF, Pascoe G, Perry DJ, Lee CA. Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency. Haemophilia 2008, 14:775-81.
-
(2008)
Haemophilia
, vol.14
, pp. 775-781
-
-
O'Connell, N.M.1
Riddell, A.F.2
Pascoe, G.3
Perry, D.J.4
Lee, C.A.5
-
93
-
-
0036489590
-
Successful use of recombinant factor VIIa in a patient with inhibitor secondary to severe factor XI deficiency
-
Lawler P, White B, Pye S. Successful use of recombinant factor VIIa in a patient with inhibitor secondary to severe factor XI deficiency. Haemophilia 2002, 8:145-8.
-
(2002)
Haemophilia
, vol.8
, pp. 145-148
-
-
Lawler, P.1
White, B.2
Pye, S.3
-
94
-
-
0030035475
-
Clinical usefulness of desmopressin for prevention of surgical bleeding in patients with symptomatic heterozygous factor XI deficiency
-
Castaman G, Ruggeri M, Rodeghiero F. Clinical usefulness of desmopressin for prevention of surgical bleeding in patients with symptomatic heterozygous factor XI deficiency. Br J Haematol 1996, 94:168-70.
-
(1996)
Br J Haematol
, vol.94
, pp. 168-170
-
-
Castaman, G.1
Ruggeri, M.2
Rodeghiero, F.3
-
95
-
-
0009479529
-
Factor XIII deficiency
-
Miloszewski KA. Factor XIII deficiency. Br J Haematol 1999, 107:468-84.
-
(1999)
Br J Haematol
, vol.107
, pp. 468-484
-
-
Miloszewski, K.A.1
-
96
-
-
0029551960
-
Antibodies to Von Willebrand factor in Von Willebrand Disease
-
Aledort LM, Hoyer LW, Reissner JM, White GC. eds, New York, Plenum Press
-
Mannucci PM, Frederici AB. Antibodies to Von Willebrand factor in Von Willebrand Disease. Inhibitors to Coagulation Factors in the 1990s 1995, 87-92. Aledort LM, Hoyer LWReissner JMWhite GC. in, eds, New York, Plenum Press
-
(1995)
Inhibitors to Coagulation Factors in the 1990s
, pp. 87-92
-
-
Mannucci, P.M.1
Frederici, A.B.2
-
97
-
-
2142649140
-
Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency
-
Lak M, Peyvandi F, Sharifian AA, Karimi K, Mannucci PM. Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency. J Thromb Haemost 2003, 1:1852-3.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1852-1853
-
-
Lak, M.1
Peyvandi, F.2
Sharifian, A.A.3
Karimi, K.4
Mannucci, P.M.5
-
98
-
-
77954859792
-
-
Available at: (last accessed 8 January 2009)
-
Behring CSL. http://www.cslbehring.co.uk/docs/1022/348/Fibrogammin%20P%20UK%20SmPC%2028-Feb-07.pdf, Available at: (last accessed 8 January 2009)
-
-
-
Behring, C.S.L.1
-
99
-
-
15144351985
-
A decade of experience with a factor XIII concentrate
-
Briggs NJ, Harman CT, Gascoigne E. A decade of experience with a factor XIII concentrate. Thromb Haemost 1997, 77(Suppl):35-6.
-
(1997)
Thromb Haemost
, vol.77
, Issue.SUPPL
, pp. 35-36
-
-
Briggs, N.J.1
Harman, C.T.2
Gascoigne, E.3
-
100
-
-
15144339960
-
Experience with fibrogammin for the long term treatment of congenital factor XIII deficiency in the USA
-
Hilgartner MW, McDonagh J, Gootenberg JE. Experience with fibrogammin for the long term treatment of congenital factor XIII deficiency in the USA. Blood 1991, 78(Suppl 1):60a.
-
(1991)
Blood
, vol.78
, Issue.SUPPL 1
-
-
Hilgartner, M.W.1
McDonagh, J.2
Gootenberg, J.E.3
-
101
-
-
0031743817
-
Factor concentrates for the treatment of factor XIII deficiency
-
Gootenberg JE. Factor concentrates for the treatment of factor XIII deficiency. Curr Opin Hematol 1998, 5:372-5.
-
(1998)
Curr Opin Hematol
, vol.5
, pp. 372-375
-
-
Gootenberg, J.E.1
-
103
-
-
33646068309
-
Safety and efficacy of fibrogammin P for the treatment of patients with severe FXIII deficiency
-
Dreyfus M, Arnuti B, Beurrier P. Safety and efficacy of fibrogammin P for the treatment of patients with severe FXIII deficiency. J Thromb Haemost 2003, 1(Suppl 1):P0299.
-
(2003)
J Thromb Haemost
, vol.1
, Issue.SUPPL 1
-
-
Dreyfus, M.1
Arnuti, B.2
Beurrier, P.3
-
104
-
-
33646047168
-
Prophylaxis in rare coagulation disorders - factor XIII deficiency
-
Nugent DJ. Prophylaxis in rare coagulation disorders - factor XIII deficiency. Thromb Res 2006, 118(Suppl 1):S23-8.
-
(2006)
Thromb Res
, vol.118
, Issue.SUPPL 1
-
-
Nugent, D.J.1
-
105
-
-
17144445992
-
Delayed umbilical bleeding - a presenting feature for factor XIII deficiency: clinical features, genetics and management
-
Anwar R, Minford A, Gallivan L, Trinh CH, Markham AF. Delayed umbilical bleeding - a presenting feature for factor XIII deficiency: clinical features, genetics and management. Pediatrics 2002, 109:e32-8.
-
(2002)
Pediatrics
, vol.109
-
-
Anwar, R.1
Minford, A.2
Gallivan, L.3
Trinh, C.H.4
Markham, A.F.5
-
106
-
-
55349104860
-
Factor XIII deficiency in a Kuwaiti child: typical presentation with delayed diagnosis
-
Al-Sharkawy IA, Aboobacker KC, Bourhama MH. Factor XIII deficiency in a Kuwaiti child: typical presentation with delayed diagnosis. Kuwait Med J 2006, 38:147-8.
-
(2006)
Kuwait Med J
, vol.38
, pp. 147-148
-
-
Al-Sharkawy, I.A.1
Aboobacker, K.C.2
Bourhama, M.H.3
-
107
-
-
0014526059
-
Diagnostic and genetic studies on fibirin stabilising factor with a new assay based on amine incorporation
-
Lorand L, Urayama T, de Kiewet J, Nossel HL. Diagnostic and genetic studies on fibirin stabilising factor with a new assay based on amine incorporation. J Clin Invest 1969, 48:1054-64.
-
(1969)
J Clin Invest
, vol.48
, pp. 1054-1064
-
-
Lorand, L.1
Urayama, T.2
de Kiewet, J.3
Nossel, H.L.4
-
108
-
-
0001286527
-
Type I autoimmune inhibitor of factor XIII in a patient with congenital factor XIII deficiency
-
Henriksson P, McDonagh J, Villa M. type I autoimmune inhibitor of factor XIII in a patient with congenital factor XIII deficiency. Thromb Haemost 1983, 50:272.
-
(1983)
Thromb Haemost
, vol.50
, pp. 272
-
-
Henriksson, P.1
McDonagh, J.2
Villa, M.3
-
109
-
-
0034486136
-
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
-
Lak M, Peyvandi F, Mannucci M. Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease. Br J Haematol 2000, 111:1236-9.
-
(2000)
Br J Haematol
, vol.111
, pp. 1236-1239
-
-
Lak, M.1
Peyvandi, F.2
Mannucci, M.3
-
110
-
-
0027302893
-
International survey of patients with von Willebrand disease and angiodysplasia
-
Fressinaud E, Meyer D. International survey of patients with von Willebrand disease and angiodysplasia. Thromb Haemost 1993, 70:546.
-
(1993)
Thromb Haemost
, vol.70
, pp. 546
-
-
Fressinaud, E.1
Meyer, D.2
-
111
-
-
37749025358
-
Gastrointestinal bleeding due to angiodysplasia in patients with type 1 von Willebrand disease: report on association and management
-
Siragusa S, Malato A, Lo Coco L. Gastrointestinal bleeding due to angiodysplasia in patients with type 1 von Willebrand disease: report on association and management. Haemophilia 2008, 14:150-2.
-
(2008)
Haemophilia
, vol.14
, pp. 150-152
-
-
Siragusa, S.1
Malato, A.2
Lo Coco, L.3
-
112
-
-
0037079717
-
Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study
-
Mannucci PM, Chediak J, Hanna W. Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study. Blood 2002, 99:450-6.
-
(2002)
Blood
, vol.99
, pp. 450-456
-
-
Mannucci, P.M.1
Chediak, J.2
Hanna, W.3
-
113
-
-
0036712293
-
Venous thromboembolism in von Willebrand disease
-
Mannucci PM. Venous thromboembolism in von Willebrand disease. Thromb Haemost 2002, 88:378-9.
-
(2002)
Thromb Haemost
, vol.88
, pp. 378-379
-
-
Mannucci, P.M.1
-
114
-
-
0036713595
-
Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease
-
Makris M, Colvin B, Gupta V. Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease. Thromb Haemost 2002, 88:387-8.
-
(2002)
Thromb Haemost
, vol.88
, pp. 387-388
-
-
Makris, M.1
Colvin, B.2
Gupta, V.3
-
115
-
-
33645980652
-
Long-term prophylaxis with intermediate-purity factor VIII concentrate (Haemate P) in a patient with type 3 von Willebrand disease and recurrent gastrointestinal bleeding
-
Coppola A, Cimino E, Conca P. Long-term prophylaxis with intermediate-purity factor VIII concentrate (Haemate P) in a patient with type 3 von Willebrand disease and recurrent gastrointestinal bleeding. Haemophilia 2006, 12:90-4.
-
(2006)
Haemophilia
, vol.12
, pp. 90-94
-
-
Coppola, A.1
Cimino, E.2
Conca, P.3
-
116
-
-
19944364505
-
Long-term prophylaxis in von Willebrand disease
-
Berntorp E, Petrini P. Long-term prophylaxis in von Willebrand disease. Blood Coagul Fibrinolysis 2005, 16(Suppl 1):S23-6.
-
(2005)
Blood Coagul Fibrinolysis
, vol.16
, Issue.SUPPL 1
-
-
Berntorp, E.1
Petrini, P.2
-
117
-
-
34548364967
-
Clinical use of Haemate®P in inherited von Willebrand's disease: a cohort study on 100 Italian patients
-
Federici AB, Castaman G, Franchini M. Clinical use of Haemate®P in inherited von Willebrand's disease: a cohort study on 100 Italian patients. Haematologica 2007, 92:944-51.
-
(2007)
Haematologica
, vol.92
, pp. 944-951
-
-
Federici, A.B.1
Castaman, G.2
Franchini, M.3
-
118
-
-
33750084376
-
For the von Willebrand disease prophylaxis network steering committee. The von Willebrand disease prophylaxis network: exploring a treatment concept
-
Berntorp E, Abshire T. For the von Willebrand disease prophylaxis network steering committee. The von Willebrand disease prophylaxis network: exploring a treatment concept. J Thromb Haemost 2006, 4:2511-2.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2511-2512
-
-
Berntorp, E.1
Abshire, T.2
-
119
-
-
33646149088
-
Secondary long-term prophylaxis in severe patients with von Willebrand's disease: an Italian cohort study
-
Federici AB, Gianniello F, Canciani MT, Mannucci PM. Secondary long-term prophylaxis in severe patients with von Willebrand's disease: an Italian cohort study. Blood 2005, 106.
-
(2005)
Blood
, vol.106
-
-
Federici, A.B.1
Gianniello, F.2
Canciani, M.T.3
Mannucci, P.M.4
-
120
-
-
0037624499
-
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients
-
Baronciani L, Cozzi G, Canciani MT. Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients. Blood Cells Mol Dis 2003, 30:264-70.
-
(2003)
Blood Cells Mol Dis
, vol.30
, pp. 264-270
-
-
Baronciani, L.1
Cozzi, G.2
Canciani, M.T.3
-
121
-
-
0035885946
-
Catheter-related deep venous thrombosis in children with hemophilia
-
Journeycake JM, Quinn CT, Miller KL. Catheter-related deep venous thrombosis in children with hemophilia. Blood 2001, 98:1727-31.
-
(2001)
Blood
, vol.98
, pp. 1727-1731
-
-
Journeycake, J.M.1
Quinn, C.T.2
Miller, K.L.3
-
122
-
-
0022364198
-
Inhibitor to factor V in severe factor V congenital deficiency
-
Mazzucconi MG, Solinas S, Chistolini A, Motta M, Mariani G. Inhibitor to factor V in severe factor V congenital deficiency. A case report. Nouv Rev Fr Hematol 1985, 27:303-5.
-
(1985)
A case report. Nouv Rev Fr Hematol
, vol.27
, pp. 303-305
-
-
Mazzucconi, M.G.1
Solinas, S.2
Chistolini, A.3
Motta, M.4
Mariani, G.5
-
123
-
-
0015351360
-
Nature of the defect in congenital factor V deficiency: study in a patient with an acquired circulating anticoagulant
-
Fratantoni JC, Hilgartner M, Nachman RL. Nature of the defect in congenital factor V deficiency: study in a patient with an acquired circulating anticoagulant. Blood 1972, 39:751-8.
-
(1972)
Blood
, vol.39
, pp. 751-758
-
-
Fratantoni, J.C.1
Hilgartner, M.2
Nachman, R.L.3
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