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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2005
Polymorphism of the D4Z4 locus associated with facioscapulohumeral muscular dystrophy 1A in Shanghai populationYu-zhou Zhang, Shun-chang Sun, Hua-cheng Wu, et al.Journal of Neuromuscular Diseases|January 15, 2023
Duchenne Muscular Dystrophy in Kazakhstan: A Journey from Diagnosis to the Treatment, the Biases and AchievementsAltynshash Jaxybayeva, Dana Chunkayeva, Bakhytkul Myrzaliyeva, et al.Human Mutation|July 23, 2009
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosisMarc Bitoun, Anne-Cécile Durieux, Bernard Prudhon, et al.Medecine Sciences : M/S|November 28, 2025
[Africa miologica: terra quasi incognita?]J Andoni Urtizberea, Ghislain Nda'h-Sekou, Sonia Nouioua, et al.Neuropathology and Applied Neurobiology|March 13, 2026
ACTA1-Related Adult-Onset Scapuloperoneal Myopathy With Cores and RodsAlexandru Caramizaru, Marion Onnée, Sergey Nikitin, et al.Neurology India|January 17, 2015
Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathyJianying Xi, Gaelle Blandin, Jiahong Lu, et al.EMBO Reports|February 25, 2006
A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathyValérie Allamand, Pascale Richard, Alain Lescure, et al.Annals of Clinical and Translational Neurology|April 16, 2016
Natural history of LGMD2A for delineating outcome measures in clinical trialsIsabelle Richard, Jean-Yves Hogrel, Daniel Stockholm, et al.Neuromuscular Disorders : NMD|October 17, 2003
Refined mapping of the HMSNR critical gene region--construction of a high-density integrated genetic and physical mapJanina Hantke, Tamara Rogers, Lisa French, et al.Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.Pageof 9