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Iranian Journal of Child Neurology|March 26, 2014
Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic CorrelationsBita Bozorgmehr, Ariana Kariminejad, Shahriar Nafissi, et al.Journal of Molecular and Cellular Cardiology|March 11, 2004
Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic propertiesDagmar I Keller, Catherine Coirault, Thomas Rau, et al.Transfusion|June 15, 2024
Evaluation of assays for nucleic acid testing for the prevention of chikungunya and dengue virus transmission by blood transfusionPierre Gallian, Isabelle Dupont, Marjorie Lacoste, et al.Neuromuscular Disorders : NMD|January 14, 2009
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutationEmmanuelle Uro-Coste, Marie-Christine Arné-Bes, Jean-François Pellissier, et al.Plos Neglected Tropical Diseases|January 13, 2017
Epidemiology of Chikungunya Virus Outbreaks in Guadeloupe and Martinique, 2014: An Observational Study in Volunteer Blood DonorsPierre Gallian, Isabelle Leparc-Goffart, Pascale Richard, et al.Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.Journal of Neuropathology and Experimental Neurology|January 6, 2007
Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathiesMuriel Herasse, Karine Parain, Isabelle Marty, et al.Vox Sanguinis|September 11, 2023
Human immunodeficiency virus, hepatitis C virus and hepatitis B virus incidence in blood donors from 2000 to 2020 in France: Trends and lessons from haemovigilance surveillanceSyria Laperche, Claire Sauvage, Pierre Gallian, et al.Human Mutation|December 11, 2008
A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathyBaijayanta Maiti, Sandrine Arbogast, Valérie Allamand, et al.European Journal of Heart Failure|December 17, 2003
Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutationJean-François Forissier, Gisèle Bonne, Christiane Bouchier, et al.Pageof 16