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Page 1
Comparison of an Innovative Rehabilitation, Combining Reduced Conventional Rehabilitation with Balneotherapy, and a Conventional Rehabilitation after Anterior Cruciate Ligament Reconstruction in Athletes.
Peultier-Celli L, Mainard D, Wein F, Paris N, Boisseau P, Ferry A, Gueguen R, Chary-Valckenaere I, Paysant J, Perrin P. Peultier-Celli L, et al. Among authors: boisseau p. Front Surg. 2017 Nov 7;4:61. doi: 10.3389/fsurg.2017.00061. eCollection 2017. Front Surg. 2017. PMID: 29164130 Free PMC article.
Does the VWF:CB Assay Help to Diagnose von Willebrand Factor Deficiency in Patients With a Bleeding Disorder of Unknown Cause?
Trossaërt M, Genre-Volot F, Horvais V, Ternisien C, Boisseau P, Fouassier M, Drillaud N, Gillet B, Péré M, Babuty A, Jeanpierre E, de Maistre E. Trossaërt M, et al. Among authors: boisseau p. Int J Lab Hematol. 2025 Feb;47(1):149-155. doi: 10.1111/ijlh.14371. Epub 2024 Sep 20. Int J Lab Hematol. 2025. PMID: 39301769 Clinical Trial.
Type 2N von Willebrand disease: genotype drives different bleeding phenotypes and treatment needs.
Daniel MY, Ternisien C, Castet S, Falaise C, D'Oiron R, Volot F, Itzhar N, Pan-Petesch B, Jeanpierre E, Paris C, Zawadzki C, Desvages M, Dupont A, Veyradier A, Repessé Y, Babuty A, Trossaërt M, Boisseau P, Denis CV, Lenting PJ, Goudemand J, Rauch A, Susen S. Daniel MY, et al. Among authors: boisseau p. J Thromb Haemost. 2024 Oct;22(10):2702-2712. doi: 10.1016/j.jtha.2024.06.020. Epub 2024 Jul 9. J Thromb Haemost. 2024. PMID: 38992343
MYH9-related disease: Assessment of the pathogenicity of a new mutation.
Antoine B, Boisseau P, Drillaud N, Eveillard M, Fouassier M. Antoine B, et al. Among authors: boisseau p. EJHaem. 2023 May 17;4(3):869-871. doi: 10.1002/jha2.715. eCollection 2023 Aug. EJHaem. 2023. PMID: 37601883 Free PMC article. No abstract available.
Biological, clinical features and modelling of heterozygous variants of glycoprotein Ib platelet subunit alpha (GP1BA) and glycoprotein Ib platelet subunit beta (GP1BB) genes responsible for constitutional thrombocytopenia.
Dib F, Quéméner A, Bayart S, Boisseau P, Babuty A, Trossaërt M, Sigaud M, Ternisien C, Drillaud N, Eveillard M, Guillet B, Béné MC, Fouassier M. Dib F, et al. Among authors: boisseau p. Br J Haematol. 2022 Dec;199(5):744-753. doi: 10.1111/bjh.18462. Epub 2022 Sep 29. Br J Haematol. 2022. PMID: 36173017 Free article.
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.
Rare pathogenic variants in WNK3 cause X-linked intellectual disability.
Küry S, Zhang J, Besnard T, Caro-Llopis A, Zeng X, Robert SM, Josiah SS, Kiziltug E, Denommé-Pichon AS, Cogné B, Kundishora AJ, Hao LT, Li H, Stevenson RE, Louie RJ, Deb W, Torti E, Vignard V, McWalter K, Raymond FL, Rajabi F, Ranza E, Grozeva D, Coury SA, Blanc X, Brischoux-Boucher E, Keren B, Õunap K, Reinson K, Ilves P, Wentzensen IM, Barr EE, Guihard SH, Charles P, Seaby EG, Monaghan KG, Rio M, van Bever Y, van Slegtenhorst M, Chung WK, Wilson A, Quinquis D, Bréhéret F, Retterer K, Lindenbaum P, Scalais E, Rhodes L, Stouffs K, Pereira EM, Berger SM, Milla SS, Jaykumar AB, Cobb MH, Panchagnula S, Duy PQ, Vincent M, Mercier S, Gilbert-Dussardier B, Le Guillou X, Audebert-Bellanger S, Odent S, Schmitt S, Boisseau P, Bonneau D, Toutain A, Colin E, Pasquier L, Redon R, Bouman A, Rosenfeld JA, Friez MJ, Pérez-Peña H, Akhtar Rizvi SR, Haider S, Antonarakis SE, Schwartz CE, Martínez F, Bézieau S, Kahle KT, Isidor B. Küry S, et al. Among authors: boisseau p. Genet Med. 2022 Sep;24(9):1941-1951. doi: 10.1016/j.gim.2022.05.009. Epub 2022 Jun 9. Genet Med. 2022. PMID: 35678782 Free article.
73 results