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.
52 pages matching periodic paralysis in this book
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LIST OF CONTRIBUTORS
INTRODUCTION Lewis P Rowland
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abnormal acid maltase Acta activity acute adult affected alcohol AMP deaminase antibodies Arch Neurol associated atrophy autosomal biochemical blood calcium cardiac carnitine carnitine deficiency cells changes chronic Clin congenital contractures creatine kinase deaminase decreased defect dehydrogenase dermatomyositis diagnosis DiMauro disease disorder distal Duchenne muscular dystrophy electromyography Engel enzyme erythrocytes exercise fatty acids fibroblasts genetic glycogen histochemical human hypokalemic increased infection inflammatory influenza involvement lactate lesions levels limb girdle lipid storage liver malignant hyperthermia McArdle's disease membrane metabolism microscopic mitochondrial muscle biopsy muscle fibers muscle weakness myofibrils myoglobin myoglobinuria myopathy myositis myotonia myotonic dystrophy necrosis necrotic nemaline Neurol Sci Neurology neuromuscular normal observed onset oxidation pathological patients Pediatr percent periodic paralysis phosphorylase plasma polymyositis potassium progressive protein pyruvate renal reported respiratory Reye syndrome sarcoplasmic serum CK skeletal muscle studies symptoms syndrome tients tion tissue ultrastructural vacuoles viral virus