Myology: basic and clinical, Volume 2
The most comprehensive reference on neuromuscular diseases and disorders! Edited by the world' s leading authority, this is the reference of choice for neurologists who a need a complete, authoritative work on muscle diseases and disorders. Features over 100 color illustrations of clinical, pathological, and imaging studies in myology. Includes important information on muscular dystrophy and inflammatory disease as well as a better understanding of mitochondrial diseases and the genetic basis of inherited diseases.
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GENERAL APPROACHES TO NEUROMUSCULAR DISEASES
Neuromuscular Transmission 442
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abnormal acid maltase Acta activity acute adult affected analysis Ann Neural antibodies antigen Arch Neural associated atrophy biochemical Brain calcium cardiac carnitine cells childhood chromosome chronic Clin clinical features CPT deficiency creatine creatine kinase decreased dehydrogenase deletion dermatomyositis detected diagnosis disease disorder distal myopathy Duchenne dystrophy Duchenne muscular dystrophy dystro dystrophin gene endomysial Engel enzyme exon fatty filaments glycogen Hum Genet human hyperkalemic hypokalemic periodic paralysis inclusion body myositis increased infection inflammatory myopathies influenza involvement kinase lesions limb girdle lipid liver lymphocytes membrane metabolic mitochondria molecular muscle biopsy muscle fibers Muscle Nerve muscle weakness mutation myalgia myofibrils myoglobinuria myotonia myotonic dystrophy necrosis nemaline Neural Sci Neurology neuromuscular normal occur onset pathological patients Pediatr percent periodic paralysis plasma polymyositis potassium progressive protein receptor reported serum CK skeletal muscle studies symptoms syndrome therapy tion type 1 fibers ultrastructural vacuoles viral virus X-linked