Claudine Mazurier

Medicine · Health Sciences

42h-index6.8kcitations165works0.02yr avg
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Research Topics

Platelet Disorders and Treatments(125), Blood groups and transfusion(66), Hemophilia Treatment and Research(61), Blood disorders and treatments(26), Blood Coagulation and Thrombosis Mechanisms(25)

Publications165 total

Purification, Biochemistry, and Structure/Function Relationships of vWf
2021
Clinical, Laboratory, and Molecular Markers of Type 2 von Willebrand Disease
2011· 8 cited
The impact of bleeding history, von Willebrand factor and PFA–100<sup>®</sup> on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM‐1VWD
British Journal of Haematology·2010· 48 citedOpen Access
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study
Journal of Thrombosis and Haemostasis·2009· 61 cited
Cross-immunoelectrophoretic analysis of heparin and gelatin binding capacity of fibronectin
Clinical & Laboratory Haematology·2008· 1 cited
Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD)
Blood·2008· 168 citedOpen Access
Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM‐1VWD)
Journal of Thrombosis and Haemostasis·2008· 159 citedOpen Access
Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD
Blood·2008· 202 citedOpen Access
Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: a comparison of fluorescent and manual techniques
Haematologica·2007· 20 citedOpen Access
Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1VWD)
Journal of Thrombosis and Haemostasis·2007· 58 citedOpen Access
A solvent/detergent‐treated and 15‐nm filtered factor VIII: a new safety standard for plasma‐derived coagulation factor concentrates
Vox Sanguinis·2007· 28 cited
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
Blood·2006· 397 citedOpen Access
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor
Journal of Thrombosis and Haemostasis·2006· 1.1k cited
Composition, Quality Control, and Labeling of Plasma-Derived Products for the Treatment of von Willebrand disease
Seminars in Thrombosis and Hemostasis·2006· 12 cited
Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ib<i>α</i> in an enzyme‐linked immunosorbent assay‐based method: performances in patients with type 2B von Willebrand disease
British Journal of Haematology·2006· 20 citedOpen Access
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)
Journal of Thrombosis and Haemostasis·2006· 523 citedOpen Access
Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
Journal of Thrombosis and Haemostasis·2006· 118 cited
Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease
Thrombosis and Haemostasis·2006· 13 cited
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide
Thrombosis and Haemostasis·2006· 33 cited
Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency
Blood Coagulation & Fibrinolysis·2005· 21 cited
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Frequent Co-authors

Jenny Goudemand(18), Dominique Meyer(15), Christine Gaucher(14), Sylvie Jorieux(12), Jeroen Eikenboom(11), I. R. Peake(11), Francesco Rodeghiero(11), Ulrich Budde(10), Reinhard Schneppenheim(10), Anne Goodeve(10), Lysiane Hilbert(10), Giancarlo Castaman(9), Javier Batlle(9), David Habart(9), Stefan Lethagen(9), M Goudemand(8), Z Vorlová(7), John Pasi(7), Augusto B. Federici(7), Claudine Caron(7)