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Muscle & Nerve|November 22, 2012
Novel FHL1 mutation in a family with reducing body myopathyTobias Schreckenbach, Wolfram Henn, Wolfram Kress, et al.
Neuropathology and Applied Neurobiology|February 6, 2026
Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular AnalysisHeidrun H Krämer-Best, Marlen C Reis, Andreas Hentschel, et al.
Biomedicines|January 8, 2025
Expanding the Molecular Genetic Landscape of Dystrophinopathies and Associated PhenotypesKatja Neuhoff, Ozge Aksel Kilicarslan, Corinna Preuße, et al.
Genes|May 28, 2022
New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1Heike Kölbel, Florian Kraft, Andreas Hentschel, et al.
Neurology|October 4, 2022
Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body MyositisFelix Kleefeld, Akinori Uruha, Anne Schänzer, et al.
International Journal of Molecular Sciences|April 13, 2023
Microscopic and Biochemical Hallmarks of <i>BICD2</i>-Associated Muscle Pathology toward the Evaluation of Novel VariantsAndreas Unger, Andreas Roos, Andrea Gangfuß, et al.
Neuropathology and Applied Neurobiology|May 11, 2021
Inflammation, fibrosis and skeletal muscle regeneration in LGMDR9 are orchestrated by macrophagesHeike Kölbel, Corinna Preuße, Lukas Brand, et al.
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