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Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Mohsenian S, Palla R, Menegatti M, Cairo A, Lecchi A, Casini A, Neerman-Arbez M, Asselta R, Scardo S, Siboni SM, Blatny J, Zapletal O, Schved JF, Giansily-Blaizot M, Halimeh S, Daoud MA, Platokouki H, Pergantou H, Schutgens REG, Van Haaften-Spoor M, Brons P, Laros-van Gorkom B, Van Pinxten E, Borhany M, Fatima N, Mikovic D, Saracevic M, Özdemir GN, Ay Y, Makris M, Lockley C, Mumford A, Harvey A, Austin S, Shapiro A, Williamson A, McGuinn C, Goldberg I, De Moerloose P, Peyvandi F. Mohsenian S, et al. Among authors: casini a. Blood Adv. 2024 Mar 26;8(6):1392-1404. doi: 10.1182/bloodadvances.2023012186. Blood Adv. 2024. PMID: 38286442 Free PMC article.
[Thrombophilia: which tests in 2012?].
de Moerloose P, Casini A, Boehlen F. de Moerloose P, et al. Among authors: casini a. Rev Med Interne. 2012 Jun;33 Suppl 1:S35-9. doi: 10.1016/j.revmed.2012.03.008. Epub 2012 Apr 11. Rev Med Interne. 2012. PMID: 22503240 Review. French. No abstract available.
Acquired factor XIII deficiency: a therapeutic challenge.
Boehlen F, Casini A, Chizzolini C, Mansouri B, Kohler HP, Schroeder V, Reber G, de Moerloose P. Boehlen F, et al. Among authors: casini a. Thromb Haemost. 2013 Mar;109(3):479-87. doi: 10.1160/TH12-08-0604. Epub 2013 Jan 10. Thromb Haemost. 2013. PMID: 23306660 Review.
Congenital fibrinogen disorders: an update.
de Moerloose P, Casini A, Neerman-Arbez M. de Moerloose P, et al. Among authors: casini a. Semin Thromb Hemost. 2013 Sep;39(6):585-95. doi: 10.1055/s-0033-1349222. Epub 2013 Jul 12. Semin Thromb Hemost. 2013. PMID: 23852822 Review.
Natural history of patients with congenital dysfibrinogenemia.
Casini A, Blondon M, Lebreton A, Koegel J, Tintillier V, de Maistre E, Gautier P, Biron C, Neerman-Arbez M, de Moerloose P. Casini A, et al. Blood. 2015 Jan 15;125(3):553-61. doi: 10.1182/blood-2014-06-582866. Epub 2014 Oct 15. Blood. 2015. PMID: 25320241 Free PMC article.
741 results