Showing results (2501-2510 of 3,410) with videos related to
Sort By:
Pageof 341
Neuromuscular Disorders : NMD|June 3, 1998
Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodiesG Ahlberg, K Borg, L Edström, et al.Neuromuscular Disorders : NMD|June 19, 1998
Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndromeM Makino, S Horai, Y Goto, et al.Neuromuscular Disorders : NMD|June 19, 1998
Congenital myopathies with inclusion bodies: a brief reviewH H GoebelNeuromuscular Disorders : NMD|May 5, 1998
Sparing of mdx extraocular muscles from dystrophic pathology is not attributable to normalized concentration or distribution of neuronal nitric oxide synthaseM Wehling, J T Stull, T J McCabe, et al.Neuromuscular Disorders : NMD|May 5, 1998
Guillain-Barré syndrome with associated thrombocytopenia: prompt response to combined corticosteroid and immunoglobulin treatmentU Corbanese, A Martinuzzi, C Possamai, et al.Neuromuscular Disorders : NMD|March 15, 2023
Epidemiology and treatment of myasthenia gravis: a retrospective study using a large insurance claims dataset in GermanyAntje Mevius, Lars Jöres, Jutta Biskup, et al.Neuromuscular Disorders : NMD|June 3, 2015
Perceived fatigue is highly prevalent and debilitating in patients with mitochondrial diseaseGráinne S Gorman, Joanna L Elson, Jane Newman, et al.Neuromuscular Disorders : NMD|September 5, 2021
Whole-body muscle MRI characteristics of LAMA2-related congenital muscular dystrophy children: An emerging patternHossam M Sakr, Nagia Fahmy, Nermine S Elsayed, et al.Neuromuscular Disorders : NMD|June 13, 2020
Characterizing cognitive-motor impairments in patients with myotonic dystrophy type 1Linard Filli, Selina Schwegler, Christian Meyer, et al.Neuromuscular Disorders : NMD|June 12, 2020
Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophyEmily C Storey, Ian Holt, Glenn E Morris, et al.Pageof 341