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Neuromuscular Disorders is a peer-reviewed medical journal that focuses on neuromuscular disease, including muscular dystrophy, spinal muscular atrophy, and myasthenia. It is the official journal of the World Muscle Society. It was established in 1991 and is published by Elsevier. Source: Wikipedia (en)
Editions published in Neuromuscular Disorders 4483
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Autosomal dominant neuromuscular disease with cylindrical spirals
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Population frequencies of inherited neuromuscular diseases—A world survey
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X-linked centronuclear myopathy: Mapping the gene to Xq28
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Multifocal avascular necrosis following high dosage steroid treatment of juvenile dermatomyositis. A case report
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Population frequencies of neuromuscular diseases—II. Amyotrophic lateral sclerosis (motor neurone disease)
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Azathioprine in myasthenia gravis: Observations in 41 patients and a review of literature
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Recent advances in the molecular pathology of familial amyloid polyneuropathy
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Myoblasts, myosins, MyoDs, and the diversification of muscle fibers
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Molecular studies of spinal muscular atrophy
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Grafts of embryonic tissue into spinal cord: a possible strategy for treating neuromuscular disorders
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Neurological disorders due to mutations of the mitochondrial genome
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Late onset lipid storage myopathy due to multiple acyl CoA dehydrogenase deficiency triggered by valproate
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Human myoblast transplantation: A simple assay for tumorigenicity
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Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus
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Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita
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Role of persisting basement membrane in the reorganization of myofibres originating from myogenic cell grafts in the rat
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Prednisone in Duchenne dystrophy
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Type III glycogen storage disease: An adult case with mild disease but complete absence of debrancher protein
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Canine X-linked muscular dystrophy: Selective involvement of muscles in neonatal dogs
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Why is the gracilis muscle relatively uninvolved in neuromuscular disorders?
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Dystrophin abnormalities in polymyositis and dermatomyositis
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Carnitine acyltransferases in normal human skeletal muscle and in muscle of patients with carnitine palmitoyltransferase deficiency
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Developmental and tissue-specific regulation of mouse dystrophin: The embryonic isoform in muscular dystrophy
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Diagnosis of muscular glycogenosis by in vivo natural abundance 13C NMR spectroscopy
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4th Colloquium on Neuromuscular Diseases (24-28 June 1991, Montpellier, France).
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Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy
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Passive avoidance behaviour deficit in the mdx mouse
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Mapping of dystrophin brain promoter: A deletion of this region is compatible with normal intellect
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Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.
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Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers
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Procainamide therapy, physical performance and energy expenditure in the Schwartz-Jampel syndrome.
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Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy
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