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Neuromuscular Disorders : NMD|November 23, 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2IN M Vieira, D Schlesinger, F de Paula, et al.Neuromuscular Disorders : NMD|May 16, 2006
An unusual pathologic feature associated with dermatomyositisJacinda B Sampson, Steven S Chin, Frederic C Clayton, et al.Neuromuscular Disorders : NMD|May 2, 2021
Congenital asymmetric distal myopathy with hemifacial weakness caused by a heterozygous large de novo mosaic deletion in nebulinLydia Sagath, Vilma-Lotta Lehtokari, Salla Välipakka, et al.Neuromuscular Disorders : NMD|May 21, 2021
Myasthenia gravis with inflammatory myopathy without elevation of creatine kinaseTakamichi Kanbayashi, Sonoko Tanaka, Yuki Hatanaka, et al.Neuromuscular Disorders : NMD|May 14, 2021
Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to goTamara Dangouloff, Eva Vrščaj, Laurent Servais, et al.Neuromuscular Disorders : NMD|May 5, 1998
Neurotrophic factors decrease the release of creatine kinase and prostaglandin E2 from metabolically stressed muscleJ D Lian, M al-Jumah, V Cwik, et al.Neuromuscular Disorders : NMD|May 5, 1998
Platelet function deficiency in Duchenne muscular dystrophyJ Forst, R Forst, H Leithe, et al.Neuromuscular Disorders : NMD|June 12, 2020
Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophyKathryn R Wagner, Hoda Z Abdel-Hamid, Jean K Mah, et al.Neuromuscular Disorders : NMD|June 12, 2020
Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolismNatalie Keller, Natalia Mendoza-Ferreira, Reza Maroofian, et al.Neuromuscular Disorders : NMD|June 12, 2020
Combining genetics, neuropsychology and neuroimaging to improve understanding of brain involvement in Duchenne muscular dystrophy - a narrative reviewNathalie DoorenweerdPageof 340