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A novel ELISA-based diagnosis of acquired von Willebrand disease with increased VWF proteolysis.
Rauch A, Caron C, Vincent F, Jeanpierre E, Ternisien C, Boisseau P, Zawadzki C, Fressinaud E, Borel-Derlon A, Hermoire S, Paris C, Lavenu-Bombled C, Veyradier A, Ung A, Vincentelli A, van Belle E, Lenting PJ, Goudemand J, Susen S. Rauch A, et al. Among authors: boisseau p. Thromb Haemost. 2016 May 2;115(5):950-9. doi: 10.1160/TH15-08-0638. Epub 2016 Jan 21. Thromb Haemost. 2016. PMID: 26791163
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. Among authors: boisseau p. Medicine (Baltimore). 2016 Mar;95(11):e3038. doi: 10.1097/MD.0000000000003038. Medicine (Baltimore). 2016. PMID: 26986123 Free PMC article.
Relevance of platelet desialylation and thrombocytopenia in type 2B von Willebrand disease: preclinical and clinical evidence.
Dupont A, Soukaseum C, Cheptou M, Adam F, Nipoti T, Lourenco-Rodrigues MD, Legendre P, Proulle V, Rauch A, Kawecki C, Bryckaert M, Rosa JP, Paris C, Ternisien C, Boisseau P, Goudemand J, Borgel D, Lasne D, Maurice P, Lenting PJ, Denis CV, Susen S, Kauskot A. Dupont A, et al. Among authors: boisseau p. Haematologica. 2019 Dec;104(12):2493-2500. doi: 10.3324/haematol.2018.206250. Epub 2019 Feb 28. Haematologica. 2019. PMID: 30819911 Free PMC article.
The homozygous variant p.Gln1311* in exon 28 of VWF is associated with the development of alloantibodies in 3 unrelated patients with type 3 VWD.
Lassalle F, Zawadzki C, Harroche A, Biron-Andréani C, Falaise C, Boisseau P, Duployez N, Jeanpierre E, Rauch A, Paris C, Susen S, Goudemand J. Lassalle F, et al. Among authors: boisseau p. Haemophilia. 2021 Jul;27(4):e491-e494. doi: 10.1111/hae.14207. Epub 2021 Jan 6. Haemophilia. 2021. PMID: 33403757 No abstract available.
Identification of von Willebrand factor D4 domain mutations in patients of Afro-Caribbean descent: In vitro characterization.
Dubois MD, Peyron I, Pierre-Louis ON, Pierre-Louis S, Rabout J, Boisseau P, de Jong A, Susen S, Goudemand J, Neviere R, Fuseau P, Christophe OD, Lenting PJ, Denis CV, Casari C. Dubois MD, et al. Among authors: boisseau p. Res Pract Thromb Haemost. 2022 Jun 15;6(4):e12737. doi: 10.1002/rth2.12737. eCollection 2022 May. Res Pract Thromb Haemost. 2022. PMID: 35734101 Free PMC article.
A Combination of Two Variants p. (Val510 =) and p. (Pro2145Thrfs * 5), Responsible for von Willebrand Disease Type 3 in a Caribbean Patient.
Dubois MD, Pierre-Louis S, Rabout J, Denis CV, Christophe O, Susen S, Goudemand J, Boisseau P, Neviere R, Pierre-Louis O. Dubois MD, et al. Among authors: boisseau p. TH Open. 2020 Oct 27;4(4):e318-e321. doi: 10.1055/s-0040-1718703. eCollection 2020 Oct. TH Open. 2020. PMID: 33134807 Free PMC article. No abstract available.
71 results