Showing results (301-310 of 390) with videos related to
Sort By:
Pageof 39
Annals of Clinical and Translational Neurology|April 17, 2025
UDP-glucose dehydrogenase variants cause dystroglycanopathyAnna M Reelfs, Carrie M Stephan, Theresa M Czech, et al.Journal of the Neurological Sciences|June 10, 2011
Mortality in Friedreich ataxiaAmy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.Journal of Clinical and Translational Science|February 16, 2026
A point-based system to determine authorship eligibility in a large clinical trial: Insights from the ISCHEMIA trial's authorship nomination systemShari Esquenazi-Karonika, Judith S Hochman, June Lyo, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Genetic mapping near the myd locus on mouse chromosome 8K A Mills, K D Mathews, T Scherpbier-Heddema, et al.Neuromuscular Disorders : NMD|May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research NetworkPangaja Paramsothy, Yinding Wang, Bo Cai, et al.Muscle & Nerve|March 21, 2022
Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015Shiny Thomas, Kristin M Conway, Olushola Fapo, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 22, 2010
Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathyRobert M Weiss, Richard E Kerber, Jane K Jones, et al.Frontiers in Genetics|May 20, 2020
Analysis of the F2LR3 (PAR4) Single Nucleotide Polymorphism (rs773902) in an Indigenous Australian PopulationDian Ningtyas, Russell J Thomson, Volga Tarlac, et al.AJNR. American Journal of Neuroradiology|June 1, 1996
Calcium 45 autoradiography and dual-isotope single-photon emission CT in a canine model of cerebral ischemia and middle cerebral artery occlusionP D Purdy, M B Horowitz, D Mathews, et al.Pageof 39