Detalhe da pesquisa
1.
Prostate biopsy and prostate cancer management in patients with haemophilia: The experience of French Haemophilia Treatment Centres.
Haemophilia
; 28(3): 437-444, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35201650
2.
Revised terminal half-life of nonacog alfa as derived from extended sampling data: A real-world study involving 64 haemophilia B patients on nonacog alfa regular prophylaxis.
Haemophilia
; 28(4): 542-547, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35420242
3.
Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A.
J Pediatr
; 234: 212-219.e3, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33676933
4.
Identification of new F8 deep intronic variations in patients with haemophilia A.
Haemophilia
; 26(5): 847-854, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32812322
5.
EQOFIX: a combined economic and quality-of-life study of hemophilia B treatments in France.
Transfusion
; 55(7): 1787-97, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25652955
6.
Antithrombotic therapy management in patients with inherited bleeding disorders and coronary artery disease: A single-centre experience.
Haemophilia
; 26(2): e34-e37, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31846115
7.
Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study.
J Thromb Haemost
; 21(8): 2126-2136, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37172732
8.
Long-Term Antithrombotic Treatments Prescribed for Cardiovascular Diseases in Patients with Hemophilia: Results from the French Registry.
Thromb Haemost
; 121(3): 287-296, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33099283
9.
Gastrointestinal bleeding from angiodysplasia in von Willebrand disease: Improved diagnosis and outcome prediction using videocapsule on top of conventional endoscopy.
J Thromb Haemost
; 19(2): 380-386, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33113216
10.
Management of von Willebrand disease with a factor VIII-poor von Willebrand factor concentrate: Results from a prospective observational post-marketing study.
J Thromb Haemost
; 18(8): 1922-1933, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32445594
11.
Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girl.
J Pediatr Endocrinol Metab
; 32(11): 1295-1298, 2019 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31472063
12.
A case of afibrinogenemia associated with A-alpha chain gene compound heterozygosity (HUMFIBRA c.[4110delA]+[3200+1G>T]).
Blood Coagul Fibrinolysis
; 18(1): 73-5, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17179831
13.
A novel hemizygous Bernard-Soulier Syndrome (BSS) mutation in the amino terminal domain of glycoprotein (GP)Ibbeta--platelet characterization and transfection studies.
Thromb Haemost
; 88(6): 1026-32, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12529755
14.
Intestinal surgery with activated recombinant factor VII prophylaxis in patients with haemophilia A and high responding inhibitors: a report of five cases.
Blood Coagul Fibrinolysis
; 15(8): 687-91, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15613924
15.
Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A.
Blood
; 107(1): 46-51, 2006 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16166584
16.
Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.
Eur J Haematol
; 75(1): 54-9, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15946311
17.
Prevalence of IgG antibodies to human parvovirus B19 in haemophilia children treated with recombinant factor (F)VIII only or with at least one plasma-derived FVIII or FIX concentrate: results from the French haemophilia cohort.
Br J Haematol
; 116(2): 383-9, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11841442