Dominique Meyer

Académie de Paris — France

Medicine · Health Sciences

41h-index5.9kcitations144works0.02yr avg
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Research Topics

Platelet Disorders and Treatments(94), Blood groups and transfusion(32), Heparin-Induced Thrombocytopenia and Thrombosis(30), Hemophilia Treatment and Research(27), Blood Coagulation and Thrombosis Mechanisms(26)

Publications144 total

Letter in response to the article “Guidance on the diagnosis and management of platelet‐type von Willebrand disease: A communication from the Platelet Physiology Subcommittee of the ISTH”
Journal of Thrombosis and Haemostasis·2021
Nanostructured Polyaniline/PLA Composites for Electrochemical Energy Storage in Flexible Conductive Thin Films
Open Scholarship Institutional Repository (Washington University in St. Louis)·2018Open Access
von Willebrand Factor Fragments
Current studies in hematology and blood transfusion·2015
Acide epsilon aminocapro�que et h�maturies des h�mophiles 3 cas d�obstruction r�nale unilat�rale passag�re
Current studies in hematology and blood transfusion·2015· 1 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
Maladie de Willebrand
Encyclopédie médico-chirurgicale. Hématologie·2008· 6 cited
Prognostic value of anti-ADAMTS13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS13 activity
Blood·2006· 293 citedOpen Access
Thrombotic Thrombocytopenic Purpura Associated with von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Children
Seminars in Thrombosis and Hemostasis·2006· 47 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
Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples
Thrombosis and Haemostasis·2006· 18 cited
Desmopressin, an unexpected link between nocturnal enuresis and inherited thrombotic thrombocytopenic purpura (Upshaw‐Schulman syndrome)
Journal of Thrombosis and Haemostasis·2005· 13 citedOpen Access
Purpura thrombotique thrombocytopénique par déficit héréditaire en ADAMTS13 (syndrome d’Upshaw-Schulman) : actualités et perspectives
Hématologie·2005· 4 cited
Thrombotic thrombocytopenic purpura related to an inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): update and perspectives
Hématologie·2005
Identification of genes involved in Ca2+ ionophore A23187-mediated apoptosis and demonstration of a high susceptibility for transcriptional repression of cell cycle genes in B lymphoblasts from a patient with Scott syndrome
BMC Genomics·2005· 9 citedOpen Access
Thrombotic thrombocytopenic purpura and its diagnosis
Journal of Thrombosis and Haemostasis·2005· 96 cited
L'année mondiale de la physique
La Lettre de l Académie des sciences·2005Open Access
Ca2+ ionophores trigger membrane remodeling without a need for store-operated Ca2+ entry
Biochemical and Biophysical Research Communications·2004· 7 cited
Thrombotic thrombocytopenic purpura with severe ADAMTS‐13 deficiency in two patients with primary antiphospholipid syndrome
Arthritis & Rheumatism·2004· 56 cited
Increased Levels of Hemostatic Proteins are Independent of Inflammation in Glycogen Storage Disease Type Ia
Journal of Pediatric Gastroenterology and Nutrition·2003· 2 cited
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Frequent Co-authors

E Fressinaud(7), Geneviève Piétu(6), Martine Wolf(5), Jean‐Pierre Girma(5), Agnès Veyradier(5), Édith Fressinaud(5), Augusto B. Federici(4), Francesco Rodeghiero(4), Bernadette Obert(4), JP Girma(4), Catherine Boyer‐Neumann(4), Danièle Kerbiriou‐Nabias(4), HR Baumgartner(4), Anne‐Sophie Ribba(4), Claudine Mazurier(4), J. Evan Sadler(3), I. R. Peake(3), Ulrich Budde(3), Agnès Veyradier(3), Florence Toti(3)