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Hugon-Rodin, Justine; Carrière, Camille; Claeyssens, Ségolène; Trillot, Nathalie; Drillaud, Nicolas; Biron-Andreani, Christine; Lavenu-Bombled, Cécile; Wieland, Anna; Flaujac, Claire; Stieltjes, Natalie; Lebreton, Aurélien; Brungs, Thomas; Hegglin, Andrea; Fiore, Mathieu; Desconclois, Céline; Gay, Valérie; Tardy-Poncet, Brigitte; Beurrier, Philippe; Barbay, Virginie; Chamouni, Pierre; ... (2023). Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest Study. Journal of thrombosis and haemostasis, 21(8), pp. 2126-2136. Wiley-Blackwell 10.1016/j.jtha.2023.04.035
Nurden, Alan T; Pillois, Xavier; Fiore, Mathieu; Alessi, Marie-Christine; Bonduel, Mariana; Dreyfus, Marie; Goudemand, Jenny; Gruel, Yves; Benabdallah-Guerida, Schéhérazade; Latger-Cannard, Véronique; Négrier, Claude; Nugent, Diane; d'Oiron, Roseline; Rand, Margaret L; Sié, Pierre; Trossaert, Marc; Alberio, Lorenzo; Martins, Nathalie; Sirvain-Trukniewicz, Peggy; Couloux, Arnaud; ... (2015). Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort. Human mutation, 36(5), pp. 548-561. Wiley-Blackwell 10.1002/humu.22776
