-
1
-
-
33947268119
-
A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency
-
Duckert F, Jung E, Shmerling D. A 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
-
2
-
-
34250758556
-
International registry on factor XIII deficiency: a basis formed mostly on European data
-
Ivaskevicius V, Seitz R, Kohler HP et al. International registry on factor XIII deficiency: a basis formed mostly on European data. Thromb Haemost 2007; 97: 914-21.
-
(2007)
Thromb Haemost
, vol.97
, pp. 914-921
-
-
Ivaskevicius, V.1
Seitz, R.2
Kohler, H.P.3
-
4
-
-
0009479529
-
Factor XIII deficiency
-
Anwar R. Factor XIII deficiency. Br J Haematol 1999; 107: 468.
-
(1999)
Br J Haematol
, vol.107
, pp. 468
-
-
Anwar, R.1
-
5
-
-
67749095010
-
Factor XIII deficiency
-
Karimi M. Factor XIII deficiency. Sem Thromb 2009; 35: 426.
-
(2009)
Sem Thromb
, vol.35
, pp. 426
-
-
Karimi, M.1
-
6
-
-
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: 32.
-
(2002)
Pediatrics
, vol.109
, pp. 32
-
-
Anwar, R.1
Minford, A.2
Gallivan, L.3
Trinh, C.H.4
Markham, A.F.5
-
7
-
-
0015498627
-
Documentation of the plasma factor XIII deficiency in man
-
Duckert F. Documentation of the plasma factor XIII deficiency in man. Ann N Y Acad Sci 1972; 202: 190-9.
-
(1972)
Ann N Y Acad Sci
, vol.202
, pp. 190-199
-
-
Duckert, F.1
-
8
-
-
0034129972
-
Maternal blood coagulation factor XIII is associated with the development of cytotrophoblastic shell
-
Asahina T, Kobayashi T, Okada Y, Goto J, Terao T. Maternal blood coagulation factor XIII is associated with the development of cytotrophoblastic shell. Placenta 2000; 21: 388-93.
-
(2000)
Placenta
, vol.21
, pp. 388-393
-
-
Asahina, T.1
Kobayashi, T.2
Okada, Y.3
Goto, J.4
Terao, T.5
-
9
-
-
34147137677
-
Congenital blood coagulation factor XIII deficiency and successful deliveries: a review of the literature
-
Asahina T, Kobayashi T, Takeuchi K, Kanayama N. Congenital blood coagulation factor XIII deficiency and successful deliveries: a review of the literature. Obstet Gynecol Surv 2007; 62: 255-60.
-
(2007)
Obstet Gynecol Surv
, vol.62
, pp. 255-260
-
-
Asahina, T.1
Kobayashi, T.2
Takeuchi, K.3
Kanayama, N.4
-
10
-
-
0033974607
-
Bleeding risk and reproductive capacity among patients with factor XIII deficiency: a case presentation and review of the literature
-
Burrows RF, Ray JG, Burrows EA. Bleeding risk and reproductive capacity among patients with factor XIII deficiency: a case presentation and review of the literature. Obstet Gynecol Surv 2000; 55: 103-8.
-
(2000)
Obstet Gynecol Surv
, vol.55
, pp. 103-108
-
-
Burrows, R.F.1
Ray, J.G.2
Burrows, E.A.3
-
11
-
-
0024368363
-
Congenital factor XIII deficiency with multiple benign breast tumours and successful pregnancy with substitutive therapy. A case report
-
Boda Z, Pfliegler G, Muszbek L et al. Congenital factor XIII deficiency with multiple benign breast tumours and successful pregnancy with substitutive therapy. A case report. Haemostasis 1989; 19: 348-52.
-
(1989)
Haemostasis
, vol.19
, pp. 348-352
-
-
Boda, Z.1
Pfliegler, G.2
Muszbek, L.3
-
12
-
-
0023191021
-
Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy. Report of a second case
-
Rodeghiero F, Castaman GC, Di Bona E, Ruggeri M, Dini E. Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy. Report of a second case. Blut 1987; 55: 45-8.
-
(1987)
Blut
, vol.55
, pp. 45-48
-
-
Rodeghiero, F.1
Castaman, G.C.2
Di Bona, E.3
Ruggeri, M.4
Dini, E.5
-
13
-
-
0031055171
-
Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA
-
Mikkola H, Muszbek L, Laiho E et al. Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA. Blood 1997; 89: 1279-87.
-
(1997)
Blood
, vol.89
, pp. 1279-1287
-
-
Mikkola, H.1
Muszbek, L.2
Laiho, E.3
-
15
-
-
0031865780
-
Studies on the role of adhesive proteins in maintaining pregnancy
-
Asahina T, Kobayashi T, Okada Y et al. Studies on the role of adhesive proteins in maintaining pregnancy. Horm Res 1998; 50: 37-45.
-
(1998)
Horm Res
, vol.50
, pp. 37-45
-
-
Asahina, T.1
Kobayashi, T.2
Okada, Y.3
-
16
-
-
0025305370
-
Congenital factor XIII deficiency with treatment of factor XIII concentrate and normal vaginal delivery
-
Kobayashi T, Terao T, Kojima T, Takamatsu J, Kamiya T, Saito H. Congenital factor XIII deficiency with treatment of factor XIII concentrate and normal vaginal delivery. Gynecol Obstet Invest 1990; 29: 235-8.
-
(1990)
Gynecol Obstet Invest
, vol.29
, pp. 235-238
-
-
Kobayashi, T.1
Terao, T.2
Kojima, T.3
Takamatsu, J.4
Kamiya, T.5
Saito, H.6
-
17
-
-
0013932934
-
Factor 13 deficiency with severe hemorrhagic diathesis
-
Fisher S, Rikover M, Naor S. Factor 13 deficiency with severe hemorrhagic diathesis. Blood 1966; 28: 34-9.
-
(1966)
Blood
, vol.28
, pp. 34-39
-
-
Fisher, S.1
Rikover, M.2
Naor, S.3
-
18
-
-
84861054202
-
Riesgo de sangrado y complicaciones ginecoobstetricas en una paciente con deficit de factor XIII. Presentacian de un caso y revision de la literatura
-
Melo CLS. Riesgo de sangrado y complicaciones ginecoobstetricas en una paciente con deficit de factor XIII. Presentacian de un caso y revision de la literatura. Medunab 2008; 11: 185.
-
(2008)
Medunab
, vol.11
, pp. 185
-
-
Melo, C.L.S.1
-
19
-
-
77952275276
-
Spinal anaesthesia and caesarean section in a patient with hypofibrinogenaemia and factor XIII deficiency
-
Hanke AA, Elsner O, Görlinger K. Spinal anaesthesia and caesarean section in a patient with hypofibrinogenaemia and factor XIII deficiency. Anaesthesia 2010; 65: 641-5.
-
(2010)
Anaesthesia
, vol.65
, pp. 641-645
-
-
Hanke, A.A.1
Elsner, O.2
Görlinger, K.3
-
20
-
-
84886641552
-
-
Successful treatment with a factor XIII-concentrate (Fibrogammin) in pregnancy in a patient with a novel factor-XIII-B-Gene-Mutation. Bangkok, Thailand: Congress World Federation of haemophilia (WFH), Available at. Accessed November 13, 2011.
-
Rott H, Halimeh S, Trobisch H. Successful treatment with a factor XIII-concentrate (Fibrogammin) in pregnancy in a patient with a novel factor-XIII-B-Gene-Mutation. Bangkok, Thailand: Congress World Federation of haemophilia (WFH), 2004. Available at http://www.gzrr.de. Accessed November 13, 2011.
-
(2004)
-
-
Rott, H.1
Halimeh, S.2
Trobisch, H.3
-
21
-
-
0035128618
-
Two novel and one recurrent missense mutation in the factor XIII A gene in two Dutch patients with factor XIII deficiency
-
Gmez-Garca EB, Poort SR, Stibbe J et al. Two novel and one recurrent missense mutation in the factor XIII A gene in two Dutch patients with factor XIII deficiency. Br J Haematol 2001; 112: 513-8.
-
(2001)
Br J Haematol
, vol.112
, pp. 513-518
-
-
Gmez-Garca, E.B.1
Poort, S.R.2
Stibbe, J.3
-
22
-
-
0025217734
-
A familial factor XIII subunit B deficiency
-
Saito M, Asakura H, Yoshida T et al. A familial factor XIII subunit B deficiency. Br J Haematol 1990; 74: 290-4.
-
(1990)
Br J Haematol
, vol.74
, pp. 290-294
-
-
Saito, M.1
Asakura, H.2
Yoshida, T.3
-
23
-
-
0036190481
-
Clinical course and management of severe congenital factor XIII deficiency
-
Meili EO. Clinical course and management of severe congenital factor XIII deficiency. Hamostaseologie 2002; 22: 48-52.
-
(2002)
Hamostaseologie
, vol.22
, pp. 48-52
-
-
Meili, E.O.1
-
24
-
-
0015063325
-
A clinical and family study of factor XIII deficiency in a New Zealand family
-
Hamer JW, Rae BA. A clinical and family study of factor XIII deficiency in a New Zealand family. Aust N Z J Med 1971; 1: 174-7.
-
(1971)
Aust N Z J Med
, vol.1
, pp. 174-177
-
-
Hamer, J.W.1
Rae, B.A.2
-
25
-
-
43149117501
-
Corpus luteal hemorrhage: an unusual manifestation of congenital factor XIII deficiency
-
Singh N, Neeta S, Gupta N et al. Corpus luteal hemorrhage: an unusual manifestation of congenital factor XIII deficiency. Haemophilia 2008; 14: 667-8.
-
(2008)
Haemophilia
, vol.14
, pp. 667-668
-
-
Singh, N.1
Neeta, S.2
Gupta, N.3
-
26
-
-
67649553799
-
An unusual clinical presentation of factor XIII deficiency and issues relating to the monitoring of factor XIII replacement therapy
-
Dargaud Y, de Mazancourt P, Rugeri L et al. An unusual clinical presentation of factor XIII deficiency and issues relating to the monitoring of factor XIII replacement therapy. Blood Coagul Fibrinolysis 2008; 19: 447-52.
-
(2008)
Blood Coagul Fibrinolysis
, vol.19
, pp. 447-452
-
-
Dargaud, Y.1
de Mazancourt, P.2
Rugeri, L.3
-
27
-
-
0039608461
-
Niccoli VS [Congenital factor XIII deficiency in pregnancy. A case report]
-
Cerenzia G, Serrao L, Carillo C, Manna MR. Niccoli VS [Congenital factor XIII deficiency in pregnancy. A case report]. Minerva Ginecol 1999; 51: 409-12.
-
(1999)
Minerva Ginecol
, vol.51
, pp. 409-412
-
-
Cerenzia, G.1
Serrao, L.2
Carillo, C.3
Manna, M.R.4
-
29
-
-
34547114773
-
Congenital factor XIII deficiency required high-dose factor XIII concentrate in late pregnancy
-
Takahashi T, Hatao K, Suzukawa M, Oji T. Congenital factor XIII deficiency required high-dose factor XIII concentrate in late pregnancy. Rinsho Ketsueki 2007; 48: 418-20.
-
(2007)
Rinsho Ketsueki
, vol.48
, pp. 418-420
-
-
Takahashi, T.1
Hatao, K.2
Suzukawa, M.3
Oji, T.4
-
30
-
-
0022811920
-
Type I and type II disease in congenital factor XIII deficiency. A further demonstration of the correctness of the classification
-
Girolami A, Cappellato MG, Lazzaro AR, Boscaro M. Type I and type II disease in congenital factor XIII deficiency. A further demonstration of the correctness of the classification. Blut 1986; 53: 411-3.
-
(1986)
Blut
, vol.53
, pp. 411-413
-
-
Girolami, A.1
Cappellato, M.G.2
Lazzaro, A.R.3
Boscaro, M.4
-
31
-
-
84866559373
-
Acute abdomen in a young girl with factor XIII deficiency perianesthetic issues
-
Chakravarty C, Sivakumaran S, Punk J, Singh N, Pandey R, Darlong V. Acute abdomen in a young girl with factor XIII deficiency perianesthetic issues. J Obstet Gynaecol India 2012; 62: 205-6.
-
(2012)
J Obstet Gynaecol India
, vol.62
, pp. 205-206
-
-
Chakravarty, C.1
Sivakumaran, S.2
Punk, J.3
Singh, N.4
Pandey, R.5
Darlong, V.6
-
32
-
-
0017725091
-
Congenital deficiency of factor XIII with normal subunit S and lack of subunit A. Report of a new family
-
Girolami A, Burul A, Sticchi A. Congenital deficiency of factor XIII with normal subunit S and lack of subunit A. Report of a new family. Acta Haematol 1977; 58: 17-26.
-
(1977)
Acta Haematol
, vol.58
, pp. 17-26
-
-
Girolami, A.1
Burul, A.2
Sticchi, A.3
-
33
-
-
0023473667
-
A new family with congenital factor XIII deficiency showing a deficit of both subunit A and B. Type I factor XIII deficiency
-
Capellato MG, Lazzaro AR, Marafioti F, Polato G, Girolami A. A new family with congenital factor XIII deficiency showing a deficit of both subunit A and B. Type I factor XIII deficiency. Haematologia (Budap) 1987; 20: 179-87.
-
(1987)
Haematologia (Budap)
, vol.20
, pp. 179-187
-
-
Capellato, M.G.1
Lazzaro, A.R.2
Marafioti, F.3
Polato, G.4
Girolami, A.5
-
34
-
-
0035353185
-
Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation
-
Koseki S, Souri M, Koga S et al. Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation. Blood 2001; 97: 2667-72.
-
(2001)
Blood
, vol.97
, pp. 2667-2672
-
-
Koseki, S.1
Souri, M.2
Koga, S.3
-
35
-
-
33745618688
-
Safety and pharmacokinetics of recombinant factor XIII-A2 administration in patients with congenital factor XIII deficiency
-
Lovejoy AE, Reynolds TC, Visich JE et al. Safety and pharmacokinetics of recombinant factor XIII-A2 administration in patients with congenital factor XIII deficiency. Blood 2006; 108: 57-62.
-
(2006)
Blood
, vol.108
, pp. 57-62
-
-
Lovejoy, A.E.1
Reynolds, T.C.2
Visich, J.E.3
-
36
-
-
34347269168
-
Congenital factor XIII deficiency in Switzerland: from the worldwide first case in 1960 to its molecular characterisation in 2005
-
Schroeder V, Durrer D, Meili E, Schubiger G, Kohler HP. Congenital factor XIII deficiency in Switzerland: from the worldwide first case in 1960 to its molecular characterisation in 2005. Swiss Med Wkly 2007; 137: 272-8.
-
(2007)
Swiss Med Wkly
, vol.137
, pp. 272-278
-
-
Schroeder, V.1
Durrer, D.2
Meili, E.3
Schubiger, G.4
Kohler, H.P.5
-
37
-
-
2142649140
-
Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency
-
Lak M, Peyvandi F, Ali Sharifian A, 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
Ali Sharifian, A.3
Karimi, K.4
Mannucci, P.M.5
-
39
-
-
33745864006
-
Congenital factor XIII deficiency in the south of Tunisia
-
Medhaffar M, Elloumi M, Guermazi S et al. Congenital factor XIII deficiency in the south of Tunisia. Pathol Biol 2006; 54: 349-52.
-
(2006)
Pathol Biol
, vol.54
, pp. 349-352
-
-
Medhaffar, M.1
Elloumi, M.2
Guermazi, S.3
-
40
-
-
63049088820
-
Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent
-
Vijapurkar M, Mota L, Shetty S, Ghosh K. Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent. Haemophilia 2009; 15: 199-202.
-
(2009)
Haemophilia
, vol.15
, pp. 199-202
-
-
Vijapurkar, M.1
Mota, L.2
Shetty, S.3
Ghosh, K.4
-
41
-
-
34548303711
-
Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations
-
Ivaskevicius V, Windyga J, Baran B et al. Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations. Haemophilia 2007; 13: 649-57.
-
(2007)
Haemophilia
, vol.13
, pp. 649-657
-
-
Ivaskevicius, V.1
Windyga, J.2
Baran, B.3
-
42
-
-
1542468827
-
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency
-
Peyvandi F, Tagliabue L, Menegatti M et al. Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency. Hum Mutat 2004; 23: 98.
-
(2004)
Hum Mutat
, vol.23
, pp. 98
-
-
Peyvandi, F.1
Tagliabue, L.2
Menegatti, M.3
-
43
-
-
84865572766
-
Successful delivery in patients with FXIII deficiency receiving prophylaxis: report of 17 cases in Iran
-
Naderi M, Eshghi P, Cohan N, Miri-Moghaddam E, Yaghmaee M, Karimi M. Successful delivery in patients with FXIII deficiency receiving prophylaxis: report of 17 cases in Iran. Haemophilia 2012; 18: 773-6.
-
(2012)
Haemophilia
, vol.18
, pp. 773-776
-
-
Naderi, M.1
Eshghi, P.2
Cohan, N.3
Miri-Moghaddam, E.4
Yaghmaee, M.5
Karimi, M.6
-
44
-
-
77953218984
-
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency
-
Ivaskevicius V, Biswas A, Loreth R et al. Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency. Haemophilia 2010; 16: 675-82.
-
(2010)
Haemophilia
, vol.16
, pp. 675-682
-
-
Ivaskevicius, V.1
Biswas, A.2
Loreth, R.3
-
45
-
-
77953196987
-
Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function
-
Ivaskevicius V, Biswas A, Bevans C et al. Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function. Haematologica 2010; 95: 956-62.
-
(2010)
Haematologica
, vol.95
, pp. 956-962
-
-
Ivaskevicius, V.1
Biswas, A.2
Bevans, C.3
-
46
-
-
84862854584
-
Factor XIII is a key molecule at the intersection of coagulation and fibrinolysis as well as inflammation and infection control
-
Ichinose A. Factor XIII is a key molecule at the intersection of coagulation and fibrinolysis as well as inflammation and infection control. Int J Hematol 2012; 95: 362-70.
-
(2012)
Int J Hematol
, vol.95
, pp. 362-370
-
-
Ichinose, A.1
-
47
-
-
33044498893
-
Pregnancy and surgical procedures in patients with factor XIII deficiency
-
Inbal A, Kenet G. Pregnancy and surgical procedures in patients with factor XIII deficiency. Biomed Prog 2003; 16: 69-71.
-
(2003)
Biomed Prog
, vol.16
, pp. 69-71
-
-
Inbal, A.1
Kenet, G.2
-
48
-
-
38449086917
-
Outcome of in vitro fertilization and ovarian response after endometrioma stripping at laparoscopy and laparotomy
-
Duru NK, Dede M, Acikel CH, Keskin U, Fidan U, Baser I. Outcome of in vitro fertilization and ovarian response after endometrioma stripping at laparoscopy and laparotomy. J Reprod Med 2007; 52: 805-9.
-
(2007)
J Reprod Med
, vol.52
, pp. 805-809
-
-
Duru, N.K.1
Dede, M.2
Acikel, C.H.3
Keskin, U.4
Fidan, U.5
Baser, I.6
-
49
-
-
0036857389
-
Poor response of ovaries with endometrioma previously treated with cystectomy to controlled ovarian hyperstimulation
-
Ho H-Y, Lee RK-K, Hwu Y-M, Lin M-H, Su J-T, Tsai Y-C. Poor response of ovaries with endometrioma previously treated with cystectomy to controlled ovarian hyperstimulation. J Assist Reprod Genet 2002; 19: 507-11.
-
(2002)
J Assist Reprod Genet
, vol.19
, pp. 507-511
-
-
Ho, H.-Y.1
Lee, R.-K.2
Hwu, Y.-M.3
Lin, M.-H.4
Su, J.-T.5
Tsai, Y.-C.6
-
50
-
-
28444439293
-
Damage to ovarian reserve associated with laparoscopic excision of endometriomas: a quantitative rather than a qualitative injury
-
Ragni G, Somigliana E, Benedetti F et al. Damage to ovarian reserve associated with laparoscopic excision of endometriomas: a quantitative rather than a qualitative injury. Am J Obstet Gynecol 2005; 193: 1908-14.
-
(2005)
Am J Obstet Gynecol
, vol.193
, pp. 1908-1914
-
-
Ragni, G.1
Somigliana, E.2
Benedetti, F.3
-
51
-
-
0344305481
-
Factor XIII A subunit-deficient mice developed severe uterine bleeding events and subsequent spontaneous miscarriages
-
Koseki-Kuno S, Yamakawa M, Dickneite G, Ichinose A. Factor XIII A subunit-deficient mice developed severe uterine bleeding events and subsequent spontaneous miscarriages. Blood 2003; 102: 4410-2.
-
(2003)
Blood
, vol.102
, pp. 4410-4412
-
-
Koseki-Kuno, S.1
Yamakawa, M.2
Dickneite, G.3
Ichinose, A.4
-
52
-
-
0034924217
-
Physiopathology and regulation of factor XIII
-
Ichinose A. Physiopathology and regulation of factor XIII. Thromb Haemost 2001; 86: 57.
-
(2001)
Thromb Haemost
, vol.86
, pp. 57
-
-
Ichinose, A.1
-
53
-
-
79960624473
-
Gynecological and obstetrical manifestations of inherited bleeding disorders in women
-
Peyvandi F, Garagiola I, Menegatti M. Gynecological and obstetrical manifestations of inherited bleeding disorders in women. J Thromb Haemost 2011; 9: 236-45.
-
(2011)
J Thromb Haemost
, vol.9
, pp. 236-245
-
-
Peyvandi, F.1
Garagiola, I.2
Menegatti, M.3
-
55
-
-
80053582150
-
Management of pregnancy and delivery in women with inherited bleeding disorders
-
Peyvandi F, Bidlingmaier C, Garagiola I. Management of pregnancy and delivery in women with inherited bleeding disorders. Semin Fetal Neonatal Med 2011; 16: 311-7.
-
(2011)
Semin Fetal Neonatal Med
, vol.16
, pp. 311-317
-
-
Peyvandi, F.1
Bidlingmaier, C.2
Garagiola, I.3
-
56
-
-
4844229372
-
The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation
-
Bolton Maggs PHB, Perry DJ, Chalmers EA et al. The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 2004; 10: 593-628.
-
(2004)
Haemophilia
, vol.10
, pp. 593-628
-
-
Bolton Maggs, P.H.B.1
Perry, D.J.2
Chalmers, E.A.3
-
57
-
-
79959656404
-
Placental abruption and perinatal mortality with preterm delivery as a mediator: disentangling direct and indirect effects
-
Ananth CV, VanderWeele TJ. Placental abruption and perinatal mortality with preterm delivery as a mediator: disentangling direct and indirect effects. Am J Epidemiol 2011; 174: 99-108.
-
(2011)
Am J Epidemiol
, vol.174
, pp. 99-108
-
-
Ananth, C.V.1
VanderWeele, T.J.2
-
58
-
-
46749153838
-
Prevalence and evolution of intracranial hemorrhage in asymptomatic term infants
-
Rooks VJ, Eaton JP, Ruess L, Petermann GW, Keck-Wherley J, Pedersen RC. Prevalence and evolution of intracranial hemorrhage in asymptomatic term infants. AJNR Am J Neuroradiol 2008; 29: 1082-9.
-
(2008)
AJNR Am J Neuroradiol
, vol.29
, pp. 1082-1089
-
-
Rooks, V.J.1
Eaton, J.P.2
Ruess, L.3
Petermann, G.W.4
Keck-Wherley, J.5
Pedersen, R.C.6
-
60
-
-
0013136726
-
Studies on the localization of adhesive proteins associated with the development of extravillous cytotrophoblast
-
Kobayashi T, Asahina T, Okada Y, Terao T. Studies on the localization of adhesive proteins associated with the development of extravillous cytotrophoblast. Placenta 1999; 20: 35-53.
-
(1999)
Placenta
, vol.20
, pp. 35-53
-
-
Kobayashi, T.1
Asahina, T.2
Okada, Y.3
Terao, T.4
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