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Catherine Pouymayou

Explore the profile of Catherine Pouymayou including associated specialties, affiliations and a list of published articles. Areas
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Articles 6
Citations 48
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Recent Articles
1.
Bertolino J, Ibrahim M, Seguier J, Masson E, Bernit E, Veit V, et al.
Haemophilia . 2018 Nov; 25(1):e42-e45. PMID: 30461133
No abstract available.
2.
Saultier P, Vidal L, Canault M, Bernot D, Falaise C, Pouymayou C, et al.
Haematologica . 2017 Mar; 102(6):1006-1016. PMID: 28255014
Congenital macrothrombocytopenia is a family of rare diseases, of which a significant fraction remains to be genetically characterized. To analyze cases of unexplained thrombocytopenia, 27 individuals from a patient cohort...
3.
Noris P, Schlegel N, Klersy C, Heller P, Civaschi E, Pujol-Moix N, et al.
Haematologica . 2014 Apr; 99(8):1387-94. PMID: 24763399
Pregnancy in women with inherited thrombocytopenias is a major matter of concern as both the mothers and the newborns are potentially at risk of bleeding. However, medical management of this...
4.
Hanss M, Pouymayou C, Blouch M, Lellouche F, Ffrench P, Rousson R, et al.
Haematologica . 2011 Apr; 96(8):1226-30. PMID: 21459789
Analyses of site-directed fibrinogen mutants expressed in several recombinant models have previously shown that both inter- and intra-chain disulfide bonds are critical for fibrinogen assembly and secretion. Four naturally occurring...
5.
Quelin F, Frere C, Pouymayou C, Morange P, de Mazancourt P, Juhan-Vague I
Blood Coagul Fibrinolysis . 2010 Jun; 20(1):84-8. PMID: 20523169
Hereditary factor XI (FXI) deficiency is an autosomal bleeding disorder of variable severity but without a clear relationship between bleeding and FXI levels or mutation location or both. In the...
6.
Morange P, Trigui N, Frere C, Chambost H, Pouymayou C, Uters M, et al.
Blood Coagul Fibrinolysis . 2009 Aug; 20(7):605-6. PMID: 19713833
A congenital FXIII A subunit deficiency was diagnosed in a male child because of umbilical bleeding at birth. Venous infusion was difficult and prophylactic FXIII infusion was delayed. At age...