Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Blood Cells, Molecules & Diseases|April 3, 2007
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCRAlexis Proust, Benoît Guillet, Capucine Picard, et al.
Thrombosis and Haemostasis|September 30, 2016
A novel platelet-type von Willebrand disease mutation (GP1BA p.Met255Ile) associated with type 2B "Malmö/New York" von Willebrand diseaseCécile Lavenu-Bombled, Corinne Guitton, Arnaud Dupuis, et al.
British Journal of Haematology|December 11, 2002
Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti-glycoprotein IIb-IIIa antibodiesIsabelle Martin, Fayçal Kriaa, Valérie Proulle, et al.
Human Genetics|September 18, 2009
Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiencyVéronique Picard, Jian-Min Chen, Brigitte Tardy, et al.
Clinical Medicine Insights. Blood Disorders|December 17, 2014
Risk factors for thrombosis in an african populationAwa Ot Fall, Valérie Proulle, Abibatou Sall, et al.
Medicine|March 18, 2016
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic PictureAgnès Veyradier, Pierre Boisseau, Edith Fressinaud, et al.
Nature Genetics|February 12, 2008
Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)David Geneviève, Valérie Proulle, Bertrand Isidor, et al.
Human Mutation|March 3, 2015
Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International CohortAlan T Nurden, Xavier Pillois, Mathieu Fiore, et al.
Pageof 2