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Thrombosis Research|July 30, 2019
How we make an accurate diagnosis of von Willebrand diseaseLuciano Baronciani, Flora PeyvandiHematology. American Society of Hematology. Education Program|November 21, 2007
TTP and ADAMTS13: When Is Testing Appropriate?Pier Mannuccio Mannucci, Flora PeyvandiResearch and Practice in Thrombosis and Haemostasis|August 21, 2025
The thrombotic paradox in congenital fibrinogen deficiencies: from pathophysiology to practiceSamin Mohsenian, Alessandro Casini, Flora PeyvandiThrombosis Research|April 10, 2020
Effect of different methods for outlier detection and rejection when calculating cut off values for diagnosis of lupus anticoagulantsVeena Chantarangkul, Flora Peyvandi, Armando Tripodi, et al.Thrombosis Research|June 8, 2018
Risk factors for inhibitor development in severe hemophilia aIsabella Garagiola, Roberta Palla, Flora PeyvandiResearch and Practice in Thrombosis and Haemostasis|February 20, 2025
Challenges and considerations of genetic testing in von Willebrand diseaseOmid Seidizadeh, Luciano Baronciani, 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 PeyvandiHematology. American Society of Hematology. Education Program|December 7, 2019
Management of rare acquired bleeding disordersMarzia Menegatti, Eugenia Biguzzi, Flora PeyvandiFrontiers in Immunology|February 8, 2021
Immune Responses to Plasma-Derived Versus Recombinant FVIII ProductsFlora Peyvandi, Syna Miri, Isabella GaragiolaJournal of Thrombosis and Haemostasis : JTH|August 10, 2021
Comparison of adverse drug reactions among four COVID-19 vaccines in Europe using the EudraVigilance database: Thrombosis at unusual sitesMaria Abbattista, Ida Martinelli, Flora PeyvandiPageof 87