Detalhe da pesquisa
1.
Acquired haemophilia A in paediatric patients: A retrospective French cohort of eight cases.
Br J Haematol
; 204(2): 606-611, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38192055
2.
Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.
Haematologica
; 2024 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38385265
3.
Oral surgery in people with inherited bleeding disorder: A retrospective study.
Haemophilia
; 2024 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38825767
4.
Severe haemorrhages leading to a diagnosis of rare bleeding disorder occur at a very young age: A study from the FranceCoag network.
Haemophilia
; 2024 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38738973
5.
Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non-severe haemophilia A.
Haemophilia
; 29(5): 1320-1333, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37410802
6.
Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross-sectional study based on the FranceCoag registry.
Haemophilia
; 29(5): 1202-1218, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37572328
7.
High Rates of Anti-αIIbß3 Antibodies Produced by a Glanzmann Thrombasthenia Patient after First and Unique Red Blood Cells Administration.
Acta Haematol
; 146(1): 44-46, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36103848
8.
A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies.
Platelets
; 32(3): 420-423, 2021 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32245340
9.
A novel rare c.-39C>T mutation in the PROS1 5'UTR causing PS deficiency by creating a new upstream translation initiation codon.
Clin Sci (Lond)
; 134(10): 1181-1190, 2020 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32426810
10.
Quality of life of siblings of adolescents with severe haemophilia (FRATHEMO): An ancillary study to the TRANSHEMO project.
Haemophilia
; 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38684456
11.
Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A.
Haematologica
; 103(1): 179-189, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29025913
12.
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
Am J Hematol
; 97(11): E393-E395, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36052950
13.
Evaluation of the potential utility of the total thrombus-formation analysis system in comparison to the platelet function analyser in subjects with primary haemostatic defects.
Br J Haematol
; 191(1): e7-e10, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32609384
14.
Intramuscular vaccination of haemophiliacs: Is it really a risk for bleeding?
Haemophilia
; 25(5): e322-e323, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31199020
15.
In vitro characterization of rare anti-αIIbß3 isoantibodies produced by patients with Glanzmann thrombasthenia that severely block fibrinogen binding and generate procoagulant platelets via complement activation.
Res Pract Thromb Haemost
; 8(1): 102253, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38268518
16.
Immunization against αIIb ß3 and αv ß3 in Glanzmann thrombasthenia patients carrying the French Gypsy mutation.
J Thromb Haemost
; 19(1): 255-261, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33090654
17.
Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): study protocol for a multicentric French national observational cross-sectional study.
BMJ Open
; 8(7): e022409, 2018 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30049701