-
1
-
-
4444269047
-
Recessively inherited coagulation disorders
-
Mannucci P.M., Duga S., Peyvandi F. Recessively inherited coagulation disorders. Blood 2004, 104:1243-1252.
-
(2004)
Blood
, vol.104
, pp. 1243-1252
-
-
Mannucci, P.M.1
Duga, S.2
Peyvandi, F.3
-
2
-
-
67749118126
-
Introduction: rare bleeding disorders: general aspects of clinical features, diagnosis, and management
-
Peyvandi F., Palla R., Menegatti M., Mannucci P.M. Introduction: rare bleeding disorders: general aspects of clinical features, diagnosis, and management. Semin Thromb Hemost 2009, 35:349-355.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 349-355
-
-
Peyvandi, F.1
Palla, R.2
Menegatti, M.3
Mannucci, P.M.4
-
3
-
-
77955030403
-
Women and bleeding disorders
-
James A.H. Women and bleeding disorders. Haemophilia 2010, 16(Suppl. 5):160-167.
-
(2010)
Haemophilia
, vol.16
, Issue.SUPPL. 5
, pp. 160-167
-
-
James, A.H.1
-
4
-
-
0038317776
-
Haemostatic changes in pregnancy
-
Bremme K.A. Haemostatic changes in pregnancy. Best Pract Res Clin Haematol 2003, 16:153-168.
-
(2003)
Best Pract Res Clin Haematol
, vol.16
, pp. 153-168
-
-
Bremme, K.A.1
-
5
-
-
69949099121
-
Pregnancy and rare bleeding disorders
-
Kadir R., Chi C., Bolton-Maggs P. Pregnancy and rare bleeding disorders. Haemophilia 2009, 15:990-1005.
-
(2009)
Haemophilia
, vol.15
, pp. 990-1005
-
-
Kadir, R.1
Chi, C.2
Bolton-Maggs, P.3
-
6
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo Y.M., Corbetta N., Chamberlain P.F., et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997, 350:485-487.
-
(1997)
Lancet
, vol.350
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
-
7
-
-
37749037035
-
Pregnancy in carriers of haemophilia
-
Chi C., Lee C.A., Shiltagh N., et al. Pregnancy in carriers of haemophilia. Haemophilia 2008, 14:56-64.
-
(2008)
Haemophilia
, vol.14
, pp. 56-64
-
-
Chi, C.1
Lee, C.A.2
Shiltagh, N.3
-
8
-
-
79951785366
-
Reproductive choices and obstetrical experience in Dutch carriers of haemophilia A and B
-
Knol H.M., Voskuilen M.A., Holterman F., et al. Reproductive choices and obstetrical experience in Dutch carriers of haemophilia A and B. Haemophilia 2011, 17:233-236.
-
(2011)
Haemophilia
, vol.17
, pp. 233-236
-
-
Knol, H.M.1
Voskuilen, M.A.2
Holterman, F.3
-
9
-
-
22744435209
-
More than menorrhagia: a review of the obstetric and gynaecological manifestations of bleeding disorders
-
James A.H. More than menorrhagia: a review of the obstetric and gynaecological manifestations of bleeding disorders. Haemophilia 2005, 11:295-307.
-
(2005)
Haemophilia
, vol.11
, pp. 295-307
-
-
James, A.H.1
-
11
-
-
0025253068
-
Glanzman's thrombasthenia: the spectrum of clinical disease
-
George J.N., Caen J.P., Nurden A.T. Glanzman's thrombasthenia: the spectrum of clinical disease. Blood 1990, 75:1383-1395.
-
(1990)
Blood
, vol.75
, pp. 1383-1395
-
-
George, J.N.1
Caen, J.P.2
Nurden, A.T.3
-
12
-
-
70449564486
-
Gynaecological and obstetrical problems in women with different bleeding disorders
-
Siboni S.M., Spreafico M., Calò L., et al. Gynaecological and obstetrical problems in women with different bleeding disorders. Haemophilia 2009, 15:1291-1299.
-
(2009)
Haemophilia
, vol.15
, pp. 1291-1299
-
-
Siboni, S.M.1
Spreafico, M.2
Calò, L.3
-
13
-
-
0034078947
-
Prenatal and peripartum management of congenital afibrinogenaemia
-
Kobayashi T., Kanayama N., Tokunaga N., et al. Prenatal and peripartum management of congenital afibrinogenaemia. Br J Haematol 2000, 109:364-366.
-
(2000)
Br J Haematol
, vol.109
, pp. 364-366
-
-
Kobayashi, T.1
Kanayama, N.2
Tokunaga, N.3
-
14
-
-
0028341120
-
Congenital coagulopathies and pregnancy: report of four pregnancies in a factor X-deficient woman
-
Kumar M., Mehta P. Congenital coagulopathies and pregnancy: report of four pregnancies in a factor X-deficient woman. Am J Hematol 1994, 46:241-244.
-
(1994)
Am J Hematol
, vol.46
, pp. 241-244
-
-
Kumar, M.1
Mehta, P.2
-
15
-
-
0030903445
-
Pregnancies in a patient with congenital absence of prothrombin activity: case report
-
Catanzarite V.A., Novotny W.F., Cousins L.M., et al. Pregnancies in a patient with congenital absence of prothrombin activity: case report. Am J Perinatol 1997, 14:135-138.
-
(1997)
Am J Perinatol
, vol.14
, pp. 135-138
-
-
Catanzarite, V.A.1
Novotny, W.F.2
Cousins, L.M.3
-
16
-
-
0034486136
-
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand's disease
-
Lak M., Peyvandi F., Mannucci P.M. Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand's disease. Br J Haematol 2000, 111:1236-1339.
-
(2000)
Br J Haematol
, vol.111
, pp. 1236-1339
-
-
Lak, M.1
Peyvandi, F.2
Mannucci, P.M.3
-
17
-
-
0032590042
-
β3-Integrin-deficient mice are a model for Glanzmann thrombasthenia showing placental defects and reduced survival
-
Hodivala-Dilke K.M., McHugh K.P., Tsakiris D.A., et al. β3-Integrin-deficient mice are a model for Glanzmann thrombasthenia showing placental defects and reduced survival. J Clin Invest 1999, 103:229-238.
-
(1999)
J Clin Invest
, vol.103
, pp. 229-238
-
-
Hodivala-Dilke, K.M.1
McHugh, K.P.2
Tsakiris, D.A.3
-
18
-
-
0036121230
-
Fibrinogen stabilizes placental-maternal attachment during embryonic development in the mouse
-
Iwaki T., Sandoval-Cooper M.J., Paiva M., et al. Fibrinogen stabilizes placental-maternal attachment during embryonic development in the mouse. Am J Pathol 2002, 160:1021-1034.
-
(2002)
Am J Pathol
, vol.160
, pp. 1021-1034
-
-
Iwaki, T.1
Sandoval-Cooper, M.J.2
Paiva, M.3
-
19
-
-
0028877613
-
Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen
-
Haverkate F., Samama M. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen. Thromb Haemost 1995, 73:151-161.
-
(1995)
Thromb Haemost
, vol.73
, pp. 151-161
-
-
Haverkate, F.1
Samama, M.2
-
20
-
-
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(Suppl. 2):37-45.
-
(1998)
Horm Res
, vol.50
, Issue.SUPPL. 2
, pp. 37-45
-
-
Asahina, T.1
Kobayashi, T.2
Okada, Y.3
-
21
-
-
38349191638
-
Intracranial haemorrhage in haemophilia A and B
-
Ljung R.C. Intracranial haemorrhage in haemophilia A and B. Br J Haematol 2008, 140:378-384.
-
(2008)
Br J Haematol
, vol.140
, pp. 378-384
-
-
Ljung, R.C.1
-
22
-
-
77953560045
-
The optimal mode of delivery for the haemophilia carrier expecting an affected infant is vaginal delivery
-
Ljung R.C. The optimal mode of delivery for the haemophilia carrier expecting an affected infant is vaginal delivery. Haemophilia 2010, 16:415-419.
-
(2010)
Haemophilia
, vol.16
, pp. 415-419
-
-
Ljung, R.C.1
-
23
-
-
77953587111
-
The optimal mode of delivery for the haemophilia carrier expecting an affected infant is caesarean delivery
-
James A.H., Hoots K. The optimal mode of delivery for the haemophilia carrier expecting an affected infant is caesarean delivery. Haemophilia 2010, 16:420-424.
-
(2010)
Haemophilia
, vol.16
, pp. 420-424
-
-
James, A.H.1
Hoots, K.2
-
24
-
-
77953556013
-
What is the optimal mode of delivery for the haemophilia carrier expecting an affected infant-vaginal delivery or caesarean delivery?
-
Madan B., Street A.M. What is the optimal mode of delivery for the haemophilia carrier expecting an affected infant-vaginal delivery or caesarean delivery?. Haemophilia 2010, 16:425-426.
-
(2010)
Haemophilia
, vol.16
, pp. 425-426
-
-
Madan, B.1
Street, A.M.2
-
25
-
-
0030820687
-
The obstetric experience of carriers of haemophilia
-
Kadir R.A., Economides D.L., Braithwaite J., Goldman E., Lee C.A. The obstetric experience of carriers of haemophilia. Br J Obstet Gynaecol 1997, 104:803-810.
-
(1997)
Br J Obstet Gynaecol
, vol.104
, pp. 803-810
-
-
Kadir, R.A.1
Economides, D.L.2
Braithwaite, J.3
Goldman, E.4
Lee, C.A.5
-
26
-
-
3943048700
-
Treatment of von Willebrand's disease
-
Mannucci P.M. Treatment of von Willebrand's disease. N Engl J Med 2004, 351:683-694.
-
(2004)
N Engl J Med
, vol.351
, pp. 683-694
-
-
Mannucci, P.M.1
-
28
-
-
77949900314
-
Platelet disorders
-
Wiley-Blackwell, Oxford, C.A. Lee, R.A. Kadir, P.A. Koudies (Eds.)
-
Philipp C.S. Platelet disorders. Inherited bleeding disorders in women 2009, 65-69. Wiley-Blackwell, Oxford. C.A. Lee, R.A. Kadir, P.A. Koudies (Eds.).
-
(2009)
Inherited bleeding disorders in women
, pp. 65-69
-
-
Philipp, C.S.1
-
29
-
-
4844229372
-
The rare coagulation disorders - review with guidelines for management from the United Kingdom haemophilia centre doctors' organisation
-
Bolton-Maggs P.H., Perry D.J., Chalmers E.A., 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.1
Perry, D.J.2
Chalmers, E.A.3
-
30
-
-
7044227596
-
Congenital hypofibrinogenemia in pregnancy: report of two cases and review of the literature
-
Frenkel E., Duksin C., Herman A., Sherman D.J. Congenital hypofibrinogenemia in pregnancy: report of two cases and review of the literature. Obstet Gynecol Surv 2004, 59:775-779.
-
(2004)
Obstet Gynecol Surv
, vol.59
, pp. 775-779
-
-
Frenkel, E.1
Duksin, C.2
Herman, A.3
Sherman, D.J.4
-
31
-
-
0035341028
-
Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombin
-
Dupuy E., Soria C., Molho P., et al. Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombin. Thromb Res 2001, 102:211-219.
-
(2001)
Thromb Res
, vol.102
, pp. 211-219
-
-
Dupuy, E.1
Soria, C.2
Molho, P.3
-
32
-
-
0026579297
-
Hereditary factor VII deficiency in pregnancy: peripartum treatment with factor VII concentrate
-
Robertson L.E., Wasserstrum N., Banez E., et al. Hereditary factor VII deficiency in pregnancy: peripartum treatment with factor VII concentrate. Am J Hematol 1992, 40:38-41.
-
(1992)
Am J Hematol
, vol.40
, pp. 38-41
-
-
Robertson, L.E.1
Wasserstrum, N.2
Banez, E.3
-
33
-
-
12544255307
-
Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency
-
Salomon O., Steinberg D.M., Tamarin I., et al. Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency. Blood Coagul Fibrinolysis 2005, 16:37-41.
-
(2005)
Blood Coagul Fibrinolysis
, vol.16
, pp. 37-41
-
-
Salomon, O.1
Steinberg, D.M.2
Tamarin, I.3
-
34
-
-
0025305370
-
Congenital factor XIII deficiency with treatment of factor XIII concentrate and normal vaginal delivery
-
Kobayashi T., Terao T., Kojima T., et al. Congenital factor XIII deficiency with treatment of factor XIII concentrate and normal vaginal delivery. Gynecol Obstet Invest 1990, 29:235-238.
-
(1990)
Gynecol Obstet Invest
, vol.29
, pp. 235-238
-
-
Kobayashi, T.1
Terao, T.2
Kojima, T.3
-
35
-
-
34147137677
-
Congenital blood coagulation factor XIII deficiency and successful deliveries: a review of the literature
-
Asahina T., Kobayashi T., Takeuchi K., et al. Congenital blood coagulation factor XIII deficiency and successful deliveries: a review of the literature. Obstet Gynecol Surv 2007, 62:255-260.
-
(2007)
Obstet Gynecol Surv
, vol.62
, pp. 255-260
-
-
Asahina, T.1
Kobayashi, T.2
Takeuchi, K.3
-
36
-
-
33646146198
-
Laboratory issues in bleeding disorders
-
Lillicrap D., Nair S.C., Srivastava A., Rodeghiero F., Pabinger I., Federici A.B. Laboratory issues in bleeding disorders. Haemophilia 2006, 12(Suppl. 3):68-75.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 68-75
-
-
Lillicrap, D.1
Nair, S.C.2
Srivastava, A.3
Rodeghiero, F.4
Pabinger, I.5
Federici, A.B.6
-
37
-
-
67849101845
-
Diagnosis and management of the fetus and neonate with alloimmune thrombocytopenia
-
Bussel J. Diagnosis and management of the fetus and neonate with alloimmune thrombocytopenia. J Thromb Haemost 2009, 7(Suppl. 1):253-257.
-
(2009)
J Thromb Haemost
, vol.7
, Issue.SUPPL. 1
, pp. 253-257
-
-
Bussel, J.1
-
38
-
-
0343603909
-
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia
-
Lak M., Keihani M., Elahi F., et al. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia. Br J Haematol 1999, 107:204-206.
-
(1999)
Br J Haematol
, vol.107
, pp. 204-206
-
-
Lak, M.1
Keihani, M.2
Elahi, F.3
-
39
-
-
2142649140
-
Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency
-
Lak M., Peyvandi F., Ali Sharifian A., Karimi K., Mannucci P.M. Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiency. J Thromb Haemost 2003, 1:1852-1853.
-
(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
-
40
-
-
77955021640
-
Bleeding disorders in neonates
-
Kenet G., Chan A.K., Soucie J.M., Kulkarni R. Bleeding disorders in neonates. Haemophilia 2010, 16(Suppl. 5):168-175.
-
(2010)
Haemophilia
, vol.16
, Issue.SUPPL. 5
, pp. 168-175
-
-
Kenet, G.1
Chan, A.K.2
Soucie, J.M.3
Kulkarni, R.4
-
41
-
-
77249125778
-
Hemostasis in neonates and children: pitfalls and dilemmas
-
Monagle P., Ignjatovic V., Savoia H. Hemostasis in neonates and children: pitfalls and dilemmas. Blood Rev 2010, 24:63-68.
-
(2010)
Blood Rev
, vol.24
, pp. 63-68
-
-
Monagle, P.1
Ignjatovic, V.2
Savoia, H.3
-
42
-
-
0030959050
-
The relevance of developmental hemostasis to hemorrhagic disorders of newborns
-
Andrew M. The relevance of developmental hemostasis to hemorrhagic disorders of newborns. Semin Perinatol 1997, 21:70-85.
-
(1997)
Semin Perinatol
, vol.21
, pp. 70-85
-
-
Andrew, M.1
-
43
-
-
33645579620
-
Developmental haemostasis. Impact for clinical haemostasis laboratories
-
Monagle P., Barnes C., Ignjatovic V., et al. Developmental haemostasis. Impact for clinical haemostasis laboratories. Thromb Haemost 2006, 95:362-372.
-
(2006)
Thromb Haemost
, vol.95
, pp. 362-372
-
-
Monagle, P.1
Barnes, C.2
Ignjatovic, V.3
-
44
-
-
77954325425
-
Association of ABO(H) and I blood group system development with von Willebrand factor and Factor VIII plasma levels in children and adolescents
-
Klarmann D., Eggert C., Geisen C., et al. Association of ABO(H) and I blood group system development with von Willebrand factor and Factor VIII plasma levels in children and adolescents. Transfusion 2010, 50:1571-1580.
-
(2010)
Transfusion
, vol.50
, pp. 1571-1580
-
-
Klarmann, D.1
Eggert, C.2
Geisen, C.3
-
45
-
-
78149239400
-
Factor XIII - an underdiagnosed deficiency - are we using the right assays?
-
Lawrie A.S., Green L., Mackie I.J., Liesner R., Machin S.J., Peyvandi F. Factor XIII - an underdiagnosed deficiency - are we using the right assays?. J Thromb Haemost 2010, 8:2478-2482.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 2478-2482
-
-
Lawrie, A.S.1
Green, L.2
Mackie, I.J.3
Liesner, R.4
Machin, S.J.5
Peyvandi, F.6
-
46
-
-
75749093010
-
Clot formation of neonates tested by thromboelastography correlates with gestational age
-
Strauss T., Levy-Shraga Y., Ravid B., et al. Clot formation of neonates tested by thromboelastography correlates with gestational age. Thromb Haemost 2010, 103:344-350.
-
(2010)
Thromb Haemost
, vol.103
, pp. 344-350
-
-
Strauss, T.1
Levy-Shraga, Y.2
Ravid, B.3
-
47
-
-
13244287712
-
In vivo thrombin generation in neonates
-
Muntean W., Leschnik B., Baier K., Cvirn G., Gallistl S. in vivo thrombin generation in neonates. J Thromb Haemost 2004, 2:2071-2072.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 2071-2072
-
-
Muntean, W.1
Leschnik, B.2
Baier, K.3
Cvirn, G.4
Gallistl, S.5
|