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Page 1
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.
Veyradier A, Boisseau P, Fressinaud E, Caron C, Ternisien C, Giraud M, Zawadzki C, Trossaert M, Itzhar-Baïkian N, Dreyfus M, d'Oiron R, Borel-Derlon A, Susen S, Bezieau S, Denis CV, Goudemand J; French Reference Center for von Willebrand disease. Veyradier A, et al. Medicine (Baltimore). 2016 Mar;95(11):e3038. doi: 10.1097/MD.0000000000003038. Medicine (Baltimore). 2016. PMID: 26986123 Free PMC article.
Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort.
Bouttefroy S, Meunier S, Milien V, Boucekine M, Chamouni P, Desprez D, Harroche A, Hochart A, Thiercelin-Legrand MF, Wibaut B, Chambost H, Rugeri L; CoDeC study group. Bouttefroy S, et al. Among authors: chamouni p. Br J Haematol. 2020 Jan;188(2):317-320. doi: 10.1111/bjh.16133. Epub 2019 Aug 14. Br J Haematol. 2020. PMID: 31414482 Free article. Review.
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.
Nguyen NAT, Auquier P, Beltran Anzola A, Harroche A, Castet S, Huguenin Y, Meunier S, Repesse Y, D'Oiron R, Rauch A, Desprez D, Spiegel A, Chamouni P, Schneider P, Baumstarck K, Boucekine M, Tabele C, Viprey M, Leroy T, Roques MA, Sannie T, Giraud N, Chambost H, Resseguier N; TRANSHEMO Study group. Nguyen NAT, et al. Among authors: chamouni p. Haemophilia. 2023 Sep;29(5):1202-1218. doi: 10.1111/hae.14841. Epub 2023 Aug 12. Haemophilia. 2023. PMID: 37572328
Surgery in rare bleeding disorders: the prospective MARACHI study.
Rousseau F, Guillet B, Mura T, Fournel A, Volot F, Chambost H, Suchon P, Frotscher B, Biron-Andréani C, Marlu R, Hezard N, Clayssens S, Boissier E, Blanc-Jouvan F, Chamouni P, Tieulie N, Rugeri L, Borel-Derlon A, de Raucourt E, Martin-Toutain I, Castet S, Lebreton A, Girault S, Helley-Russick D, D'Oiron R, Schved JF, Giansily-Blaizot M. Rousseau F, et al. Among authors: chamouni p. Res Pract Thromb Haemost. 2023 Sep 6;7(7):102199. doi: 10.1016/j.rpth.2023.102199. eCollection 2023 Oct. Res Pract Thromb Haemost. 2023. PMID: 37867585 Free PMC article.
Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study.
Hugon-Rodin J, Carrière C, Claeyssens S, Trillot N, Drillaud N, Biron-Andreani C, Lavenu-Bombled C, Wieland A, Flaujac C, Stieltjes N, Lebreton A, Brungs T, Hegglin A, Fiore M, Desconclois C, Gay V, Tardy-Poncet B, Beurrier P, Barbay V, Chamouni P, Maistre E, Simurda T, Casini A. Hugon-Rodin J, et al. Among authors: chamouni p. J Thromb Haemost. 2023 Aug;21(8):2126-2136. doi: 10.1016/j.jtha.2023.04.035. Epub 2023 May 11. J Thromb Haemost. 2023. PMID: 37172732 Free article.
Factor XII deficiency evaluated by thrombin generation assay.
Feugray G, Kasonga F, Chamouni P, Barbay V, Fresel M, Hélène Chretien M, Brunel S, Le Cam Duchez V, Billoir P. Feugray G, et al. Among authors: chamouni p. Clin Biochem. 2022 Feb;100:42-47. doi: 10.1016/j.clinbiochem.2021.11.014. Epub 2021 Nov 26. Clin Biochem. 2022. PMID: 34843733 Clinical Trial.
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: chamouni p. Haemophilia. 2021 Sep;27(5):e641-e644. doi: 10.1111/hae.14377. Epub 2021 Jul 13. Haemophilia. 2021. PMID: 34255402 No abstract available.
Quality of life of siblings of adolescents with severe haemophilia (FRATHEMO): An ancillary study to the TRANSHEMO project.
Nguyen NAT, Auquier P, Beltran Anzola A, Harroche A, Huguenin Y, Hochart A, Meunier S, Frotscher B, Nguyen P, Schneider P, Berger C, Lebreton A, Vanderbecken S, De Raucourt E, D'Oiron R, Oudot-Challard C, Baumstarck K, Boucekine M, Tabélé C, Rosso-Delsemme N, Sannié T, Giraud N, Chambost H, Resseguier N; FRATHEMO Study group. Nguyen NAT, et al. Haemophilia. 2024 Jul;30(4):1071-1076. doi: 10.1111/hae.15023. Epub 2024 Apr 29. Haemophilia. 2024. PMID: 38684456 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: chamouni 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
41 results