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Scientific Reports|February 26, 2021
Mitochondrial function and oxidative stress markers in higher-frequency episodic migraineElena C Gross, Niveditha Putananickal, Anna-Lena Orsini, et al.Degenerative Neurological and Neuromuscular Disease|March 24, 2025
A Hypothesized Therapeutic Role of (Z)-Endoxifen in Duchenne Muscular Dystrophy (DMD)H Lawrence Remmel, Sandra S Hammer, Laurence A Neff, et al.Journal of Magnetic Resonance Imaging : JMRI|December 25, 2010
Quantification of fat infiltration in oculopharyngeal muscular dystrophy: comparison of three MR imaging methodsMonika Gloor, Susanne Fasler, Arne Fischmann, et al.Human Molecular Genetics|April 1, 2005
Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitroHarald Bär, Dirk Fischer, Bertrand Goudeau, et al.Human Mutation|December 24, 2008
How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathyChristoph S Clemen, Dirk Fischer, Jens Reimann, et al.Neuromuscular Disorders : NMD|February 22, 2014
Skeletal muscle MRI of the lower limbs in congenital muscular dystrophy patients with novel POMT1 and POMT2 mutationsPatricia Hafner, Ulrike Bonati, Arne Fischmann, et al.European Journal of Pediatrics|July 3, 2024
Tamoxifen may contribute to preserve cardiac function in Duchenne muscular dystrophyBettina C Henzi, Sebastiano A G Lava, Carlos Spagnuolo, et al.Journal of Neuromuscular Diseases|March 25, 2025
Automated analysis of quantitative muscle MRI and its reliability in patients with Duchenne muscular dystrophySara Nagy, Olga Kubassova, Patricia Hafner, et al.Neuromuscular Disorders : NMD|March 23, 2010
Reverse protein arrays as novel approach for protein quantification in muscular dystrophiesClaudia Escher, Hanns Lochmüller, Dirk Fischer, et al.Journal of Patient-Reported Outcomes|July 18, 2020
Health-related quality of life, self-reported impairments and activities of daily living in relation to muscle function in post-polio syndromeVanya Gocheva, Patricia Hafner, Anna-Lena Orsini, et al.Pageof 10