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Blood|February 26, 2015
Rare bleeding disorders: diagnosis and treatmentRoberta Palla, Flora Peyvandi, Amy D ShapiroThrombosis Research|June 8, 2018
Risk factors for inhibitor development in severe hemophilia aIsabella Garagiola, Roberta Palla, Flora PeyvandiPrenatal Diagnosis|September 17, 2003
Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency--misdiagnosis by direct sequence analysis using a PCR productIsabella Garagiola, Roberta Palla, Flora PeyvandiSeminars in Thrombosis and Hemostasis|July 27, 2013
Rare bleeding disorders: worldwide efforts for classification, diagnosis, and managementFlora Peyvandi, Marzia Menegatti, Roberta PallaResearch and Practice in Thrombosis and Haemostasis|June 17, 2026
Shaping hemophilia care: lessons and legacy of the SIPPET trial after 10 yearsFlora Peyvandi, Roberta Palla, Isabella Garagiola, et al.Seminars in Thrombosis and Hemostasis|July 15, 2009
Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and managementFlora Peyvandi, Roberta Palla, Marzia Menegatti, et al.Haematologica|February 1, 2020
An international registry of patients with plasminogen deficiency (HISTORY)Amy D Shapiro, Marzia Menegatti, Roberta Palla, et al.Research and Practice in Thrombosis and Haemostasis|June 12, 2025
Effect of DNA methylation on inhibitor development in people with hemophilia A treated with FVIII concentratesHimani Chand, Shermarke Hassan, Andrea Cairo, et al.Human Mutation|October 23, 2009
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpuraLuca A Lotta, Isabella Garagiola, Roberta Palla, et al.Research and Practice in Thrombosis and Haemostasis|March 9, 2023
Prevalence of selected bleeding and thrombotic events in persons with hemophilia versus the general population: A scoping reviewAmy D Shapiro, Brandon M Hardesty, Flora Peyvandi, et al.Pageof 58