Showing results (111-120 of 154) with videos related to
Sort By:
Pageof 16
Frontiers in Immunology|October 24, 2022
Inflammatory profile of convalescent plasma to treat COVID: Impact of amotosalen/UVA pathogen reduction technologyFabrice Cognasse, Hind Hamzeh-Cognasse, Anne-Claire Duchez, et al.Journal De La Societe De Biologie|August 24, 2005
[Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene]Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.Plos One|January 18, 2013
A mutation causes MuSK reduced sensitivity to agrin and congenital myastheniaAsma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, et al.Clinical Genetics|June 28, 2019
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlationsFlavie Ader, Pascal De Groote, Patricia Réant, et al.Human Molecular Genetics|October 22, 2004
MUSK, a new target for mutations causing congenital myasthenic syndromeFrédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.American Journal of Human Genetics|July 28, 2009
Identification of an agrin mutation that causes congenital myasthenia and affects synapse functionCaroline Huzé, Stéphanie Bauché, Pascale Richard, et al.Brain : a Journal of Neurology|November 26, 2013
Natural history of pulmonary function in collagen VI-related myopathiesA Reghan Foley, Susana Quijano-Roy, James Collins, et al.Clinical Genetics|November 25, 2018
Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneityPascale Richard, Flavie Ader, Maguelonne Roux, et al.The Journal of Molecular Diagnostics : JMD|May 17, 2022
Long-Reads Sequencing Strategy to Localize Variants in TTN Repeated DomainsAurélien Perrin, Charles Van Goethem, Corinne Thèze, et al.Journal of Cardiac Failure|June 5, 2021
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction: Phenotype/Genotype of NoncompactionMarie Cambon-Viala, Hilla Gerard, Karine Nguyen, et al.Pageof 16