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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 3
2001 5
2002 2
2003 1
2004 1
2005 1
2006 2
2007 1
2008 2
2009 6
2010 6
2011 1
2013 1
2014 4
2015 5
2016 2
2017 2
2018 4
2019 2
2020 4
2021 3
2022 3
2023 9
2024 2

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66 results

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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.
[Thromboembolic disease in pediatric oncology].
Theron A, Biron-Andreani C, Haouy S, Saumet L, Saguintah M, Jeziorski E, Sirvent N. Theron A, et al. Among authors: biron andreani c. Arch Pediatr. 2018 Feb;25(2):139-144. doi: 10.1016/j.arcped.2017.10.029. Epub 2018 Jan 8. Arch Pediatr. 2018. PMID: 29325825 Review. French.
[Primary hemostasis exploration].
Stepanian A, Biron-Andréani C. Stepanian A, et al. Among authors: biron andreani c. Ann Biol Clin (Paris). 2001 Nov-Dec;59(6):725-35. Ann Biol Clin (Paris). 2001. PMID: 11713017 Free article. Review. French.
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: biron andreani c. 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
Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders.
Trossaert M, Chamouard V, Biron-Andreani C, Casini A, De Mazancourt P, De Raucourt E, Drillaud N, Frotscher B, Guillet B, Lebreton A, Roussel-Robert V, Rugeri L, Dargaud Y. Trossaert M, et al. Among authors: biron andreani c. Eur J Haematol. 2023 Jun;110(6):584-601. doi: 10.1111/ejh.13941. Epub 2023 Feb 20. Eur J Haematol. 2023. PMID: 36748278 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. 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: biron andreani c. 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.
66 results