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Rare coagulation deficiencies.
Peyvandi F, Duga S, Akhavan S, Mannucci PM. Peyvandi F, et al. Haemophilia. 2002 May;8(3):308-21. doi: 10.1046/j.1365-2516.2002.00633.x. Haemophilia. 2002. PMID: 12010428 Review.
Genetic diagnosis of haemophilia and other inherited bleeding disorders.
Peyvandi F, Jayandharan G, Chandy M, Srivastava A, Nakaya SM, Johnson MJ, Thompson AR, Goodeve A, Garagiola I, Lavoretano S, Menegatti M, Palla R, Spreafico M, Tagliabue L, Asselta R, Duga S, Mannucci PM. Peyvandi F, et al. Haemophilia. 2006 Jul;12 Suppl 3:82-9. doi: 10.1111/j.1365-2516.2006.01263.x. Haemophilia. 2006. PMID: 16684001 Review.
Central nervous system bleeding in patients with rare bleeding disorders.
Siboni SM, Zanon E, Sottilotta G, Consonni D, Castaman G, Mikovic D, Biondo F, Tagliaferri A, Iorio A, Mannucci PM, Peyvandi F. Siboni SM, et al. Among authors: peyvandi f. Haemophilia. 2012 Jan;18(1):34-8. doi: 10.1111/j.1365-2516.2011.02545.x. Epub 2011 May 4. Haemophilia. 2012. PMID: 21539694
Role of von Willebrand factor in the haemostasis.
Peyvandi F, Garagiola I, Baronciani L. Peyvandi F, et al. Blood Transfus. 2011 May;9 Suppl 2(Suppl 2):s3-8. doi: 10.2450/2011.002S. Blood Transfus. 2011. PMID: 21839029 Free PMC article. Review. No abstract available.
761 results