Evaluation and Treatment of Myopathies
F.A. Davis, 1995 - Maladies neuromusculaires - 434 pages
Evaluation and Treatment of Myopathies provides practical information on muscle disease, emphasizing clinical features and diagnostic approaches, and highlighting the latest information on treatment.
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VOLUNTARY CONTROL OF MOTOR UNIT
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abnormalities Ann Neurol Arch Neurol associated atrophy autosomal dominant autosomal recessive cardiac carnitine cause cells central core disease centronuclear centronuclear myopathy chromosome chronic CK level Clin CLINICAL FEATURES congenital myopathy connective tissue defect deficiency dermatomyositis diagnosis disorders Duchenne dystrophy effect elevated Engl enzyme exercise fatigue gene genetic glycogen Griggs RC hyperkalemia hypokalemic periodic paralysis inclusion body myositis increased inflammatory myopathy kinase LABORATORY FEATURES limb-girdle malignant hyperthermia McArdle's disease membrane ment metabolic mitochondrial myopathies motor unit potentials mtDNA muscle biopsy muscle disease muscle fibers Muscle Nerve muscle pain muscle weakness muscular dys muscular dystrophy mutation myalgia myoglobinuria myotonia congenita myotonic dystrophy nemaline Neurol Sci Neurology neuromuscular disease neuropathy normal occur opathy paramyotonia PATHOGENESIS patients periodic paralysis peripheral polymyositis potassium prednisone protein proximal weakness renal respiratory result skeletal muscle studies symptoms syndrome Table tients tion treatment type 1 fibers usually