Detalhe da pesquisa
1.
Practical aspects of factor concentrate use in patients with von Willebrand disease undergoing invasive procedures: a European survey.
Haemophilia
; 22(5): 739-51, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27292438
2.
Practical aspects of DDAVP use in patients with von Willebrand Disease undergoing invasive procedures: a European survey.
Haemophilia
; 22(1): 110-20, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26207933
3.
Efficacy and safety of pegylated full-length recombinant factor VIII with extended half-life for perioperative haemostasis in haemophilia A patients.
Haemophilia
; 22(4): e251-8, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27328112
4.
Efficacy and safety of long-acting recombinant fusion protein linking factor IX with albumin in haemophilia B patients undergoing surgery.
Haemophilia
; 22(4): e259-66, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27333467
5.
Diagnosis of inherited von Willebrand disease: comparison of two methodologies and analysis of the discrepancies.
Haemophilia
; 20(4): 559-67, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25077350
6.
Sequential combined bypassing therapy is safe and effective in the treatment of unresponsive bleeding in adults and children with haemophilia and inhibitors.
Haemophilia
; 17(4): 630-5, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21323801
7.
Replacement therapy in inherited factor VII deficiency: occurrence of adverse events and relation with surgery.
Haemophilia
; 21(6): e513-7, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26249164
8.
Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report.
Haemophilia
; 16(5): 747-66, 2010 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20398077
9.
Prevalence, follow-up and clinical significance of the anticardiolipin antibodies in normal subjects.
Thromb Haemost
; 72(2): 209-13, 1994 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-7831653
10.
Abnormal structure of von Willebrand factor in myeloproliferative syndrome is associated to either thrombotic or bleeding diathesis.
Thromb Haemost
; 58(2): 753-7, 1987 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-3499682
11.
Effect of dextran on factor VIII/von Willebrand factor structure and function.
Thromb Haemost
; 54(3): 697-9, 1985 Oct 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-2418526
12.
High levels of plasma FVIII and vWF in the toxic epidemic syndrome patients.
Thromb Haemost
; 62(2): 690-3, 1989 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-2510349
13.
Pharmacogenetics of acenocoumarol in patients with extreme dose requirements.
J Thromb Haemost
; 8(5): 1012-7, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20149073
14.
Secretion of von Willebrand factor from platelets.
Methods Enzymol
; 169: 244-51, 1989.
Artigo
em Inglês
| MEDLINE | ID: mdl-2785631
15.
Platelet and plasma von Willebrand factor: structural differences.
Thromb Res
; 44(1): 125-8, 1986 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-3491444
16.
Primary leiomyosarcoma of the superior vena cava with massive thrombosis treated by local fibrinolysis.
Br J Radiol
; 65(780): 1131-2, 1992 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-1286424
17.
[Complement and hereditary angioedema. Mechanism of their relationship and danazol influence (author's transl)]. / Complemento y edema angioneurótico hereditario. Mecanismo de sus interrelaciones e influencia del danazol.
Med Clin (Barc)
; 77(9): 380-5, 1981 Nov 25.
Artigo
em Espanhol
| MEDLINE | ID: mdl-7329148
18.
[Therapy of disseminated intravascular coagulation in acute promyelocytic leukemias. Apropos of 19 cases]. / Terapéutica de la coagulación intravascular diseminada en las leucemias agudas promielocíticas. A propósito de 19 casos.
Sangre (Barc)
; 38(6): 449-53, 1993 Dec.
Artigo
em Espanhol
| MEDLINE | ID: mdl-8171380
19.
Advances in the therapy of von Willebrand disease.
Haemophilia
; 8(3): 301-7, 2002 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12010427
20.
Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII.
Am J Hematol
; 40(1): 20-7, 1992 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-1566742