Maria A. Lazzari
B, Argentina
Last Updated: 09/26/2026
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Found 8 publications
Combined effects of two mutations in von Willebrand disease 2M phenotype.
Journal: Research and practice in thrombosis and haemostasis
Published: June 05, 2017
Phenotypic Parameters in Genotypically Selected Type 2B von Willebrand Disease Patients: A Large, Single-Center Experience Including a New Novel Mutation.
Journal: Seminars in thrombosis and hemostasis
Published: December 16, 2016
Identification of p.W246L as a novel mutation in the GP1BA gene responsible for platelet-type von Willebrand disease.
Journal: Seminars in thrombosis and hemostasis
Published: January 30, 2014
Clinical profile of the association of P.R1205h and P.R924q in a patient with von Willebrand's disease.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: January 18, 2013
Von Willebrand factor (VWF) as a risk factor for bleeding and thrombosis.
Journal: Hematology (Amsterdam, Netherlands)
Published: April 18, 2012
Diagnosis and management of von Willebrand disease in a single institution of Argentina.
Journal: Seminars in thrombosis and hemostasis
Published: November 22, 2011
A new ADAMTS13 missense mutation (D1362V) in thrombotic thrombocytopenic purpura diagnosed during pregnancy.
Journal: Thrombosis and haemostasis
Published: November 11, 2011
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Last Updated: 09/26/2026