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1.
Efficacy and safety of turoctocog alfa in patients with hemophilia A requiring surgical procedures: A multicentre retrospective study.
Transfusion
; 63(12): 2321-2327, 2023 12.
Article
in English
| MEDLINE | ID: mdl-37850587
2.
A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.
Haemophilia
; 29(4): 1113-1120, 2023 Jul.
Article
in English
| MEDLINE | ID: mdl-37252892
3.
rFVIII-Fc in severe haemophilia A: The incentive switch in case of high risk of joint bleedings.
Eur J Clin Invest
; 52(10): e13824, 2022 Oct.
Article
in English
| MEDLINE | ID: mdl-35699345
4.
Efficacy and safety of a recombinant Von Willebrand Factor treatment in patients with inherited Von Willebrand Disease requiring surgical procedures.
Haemophilia
; 27(2): 270-276, 2021 Mar.
Article
in English
| MEDLINE | ID: mdl-33550648
5.
Bleeding complications during pregnancy and delivery in haemophilia carriers and their neonates in Western France: An observational study.
Haemophilia
; 26(6): 1046-1055, 2020 Nov.
Article
in English
| MEDLINE | ID: mdl-32842170
6.
Spectrum of the mutations in Bernard-Soulier syndrome.
Hum Mutat
; 35(9): 1033-45, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24934643
7.
Bleeding risk for patients with haemophilia under antithrombotic therapy. Results of the French multicentric study ERHEA.
Br J Haematol
; 185(4): 764-767, 2019 05.
Article
in English
| MEDLINE | ID: mdl-30338508
8.
Genotype-dependent response to desmopressin in hemophilia A and proposal of a predictive response score.
Thromb Haemost
; 2024 May 17.
Article
in English
| MEDLINE | ID: mdl-38759975
9.
Key Drivers of Coagulation Factor Use in Von Willebrand Disease During Hospitalization: An Overview of the French BERHLINGO Cohort.
Clin Drug Investig
; 44(1): 35-49, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-38036930
10.
Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study.
J Thromb Haemost
; 21(8): 2126-2136, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37172732
11.
Gynecological and obstetric outcome in the French cohort of women with factor XIII deficiency.
Thromb Res
; 191: 22-25, 2020 07.
Article
in English
| MEDLINE | ID: mdl-32360976
12.
[Partial thrombosis of the corpus cavernosum. Must a clotting disorder be systematically investigated?]. / Thrombose partielle du corps caverneux. Faut-il rechercher systématiquement une anomalie de la coagulation?
Prog Urol
; 17(4): 866-8, 2007 Jun.
Article
in French
| MEDLINE | ID: mdl-17634004
13.
Immune tolerance induction with highly purified plasma-derived factor VIII containing von Willebrand factor in hemophilia A patients with high-responding inhibitors.
Haematologica
; 90(9): 1288-90, 2005 Sep.
Article
in English
| MEDLINE | ID: mdl-16154861
14.
Compound heterozygous mutations of the TNXB gene cause primary myopathy.
Neuromuscul Disord
; 23(8): 664-9, 2013 Aug.
Article
in English
| MEDLINE | ID: mdl-23768946
15.
Compound heterozygous mutations of the TNXB gene cause primary myopathy. Response.
Neuromuscul Disord
; 24(1): 89, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24295814
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