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Afibrinogenemia with two compound heterozygous mutations in FGA gene.
Feugray G, Billoir P, Casini A, Neerman-Arbez M, Barbay V, Chamouni P, Schneider P, Le Cam Duchez V. Feugray G, et al. Among authors: billoir p. Haemophilia. 2021 Sep;27(5):e641-e644. doi: 10.1111/hae.14377. Epub 2021 Jul 13. Haemophilia. 2021. PMID: 34255402 No abstract available.
Evaluation of thrombin generation assay in factor XI deficiency.
Kasonga F, Feugray G, Chamouni P, Barbay V, Fresel M, Chretien MH, Brunel S, Le Cam Duchez V, Billoir P. Kasonga F, et al. Among authors: billoir p. Clin Chim Acta. 2021 Dec;523:348-354. doi: 10.1016/j.cca.2021.10.021. Epub 2021 Oct 17. Clin Chim Acta. 2021. PMID: 34670127
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