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Three-year outcomes of valoctocogene roxaparvovec gene therapy for hemophilia A.
Madan B, Ozelo MC, Raheja P, Symington E, Quon DV, Leavitt AD, Pipe SW, Lowe G, Kenet G, Reding MT, Mason J, Wang M, von Drygalski A, Klamroth R, Shapiro S, Chambost H, Dunn AL, Oldenburg J, Chou SC, Peyvandi F, Millar CM, Osmond D, Yu H, Dashiell-Aje E, Robinson TM, Mahlangu J. Madan B, et al. Among authors: peyvandi f. J Thromb Haemost. 2024 Apr 12:S1538-7836(24)00184-3. doi: 10.1016/j.jtha.2024.04.001. Online ahead of print. J Thromb Haemost. 2024. PMID: 38614387 Free article.
Pharmacokinetics and safety of fibrinogen concentrate.
Manco-Johnson MJ, Dimichele D, Castaman G, Fremann S, Knaub S, Kalina U, Peyvandi F, Piseddu G, Mannucci P; FIBRINOGEN CONCENTRATE STUDY GROUP. Manco-Johnson MJ, et al. Among authors: peyvandi f. J Thromb Haemost. 2009 Dec;7(12):2064-9. doi: 10.1111/j.1538-7836.2009.03633.x. Epub 2009 Oct 5. J Thromb Haemost. 2009. PMID: 19804533 Free article. Clinical Trial.
Fibrinogen replacement therapy for congenital fibrinogen deficiency.
Bornikova L, Peyvandi F, Allen G, Bernstein J, Manco-Johnson MJ. Bornikova L, et al. Among authors: peyvandi f. J Thromb Haemost. 2011 Sep;9(9):1687-704. doi: 10.1111/j.1538-7836.2011.04424.x. J Thromb Haemost. 2011. PMID: 21711446 Free article. Review.
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders.
Peyvandi F, Palla R, Menegatti M, Siboni SM, Halimeh S, Faeser B, Pergantou H, Platokouki H, Giangrande P, Peerlinck K, Celkan T, Ozdemir N, Bidlingmaier C, Ingerslev J, Giansily-Blaizot M, Schved JF, Gilmore R, Gadisseur A, Benedik-Dolničar M, Kitanovski L, Mikovic D, Musallam KM, Rosendaal FR; European Network of Rare Bleeding Disorders Group. Peyvandi F, et al. J Thromb Haemost. 2012 Apr;10(4):615-21. doi: 10.1111/j.1538-7836.2012.04653.x. J Thromb Haemost. 2012. PMID: 22321862 Free article.
Management of bleeding disorders in adults.
Peyvandi F, Klamroth R, Carcao M, Federici AB, DI Minno G, Jiménez-Yuste V, Rodriguez Merchán EC. Peyvandi F, et al. Haemophilia. 2012 May;18 Suppl 2:24-36. doi: 10.1111/j.1365-2516.2012.02797.x. Haemophilia. 2012. PMID: 22530576 Review.
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis.
Lotta LA, Tuana G, Yu J, Martinelli I, Wang M, Yu F, Passamonti SM, Pappalardo E, Valsecchi C, Scherer SE, Hale W 4th, Muzny DM, Randi G, Rosendaal FR, Gibbs RA, Peyvandi F. Lotta LA, et al. Among authors: peyvandi f. J Thromb Haemost. 2013 Jul;11(7):1228-39. doi: 10.1111/jth.12291. J Thromb Haemost. 2013. PMID: 23648131 Free article.
Future of coagulation factor replacement therapy.
Peyvandi F, Garagiola I, Seregni S. Peyvandi F, et al. J Thromb Haemost. 2013 Jun;11 Suppl 1:84-98. doi: 10.1111/jth.12270. J Thromb Haemost. 2013. PMID: 23809113 Free article. Review.
732 results