Myology: Basic and Clinical, Volume 2 |
Contents
Contributors xiii | 1121 |
GENERAL APPROACHES TO NEUROMUSCULAR DISEASES | 1122 |
Neuromuscular Transmission 442 | 1124 |
Copyright | |
42 other sections not shown
Common terms and phrases
abnormal acid maltase Acta activity acute adult affected analysis Ann Neurol antibodies antigen Arch Neurol associated atrophy biochemical Brain calcium cardiac carnitine cells childhood chromosome chronic Clin clinical features congenital muscular dystrophy CPT deficiency creatine kinase decreased deletion dermatomyositis detected diagnosis disease disorder distal myopathy Duchenne dystrophy Duchenne muscular dystrophy dystro dystrophin gene Engel enzyme exon filaments glycogen Hum Genet human hyperkalemic hypokalemic periodic paralysis inclusion body myositis increased infection inflammatory myopathies influenza involvement lesions limb girdle lipid liver lymphocytes membrane metabolic mitochondria mitochondrial molecular muscle biopsy muscle fibers Muscle Nerve muscle weakness mutation myalgia myofibrils myoglobinuria myotonia myotonic dystrophy necrosis necrotic fibers nemaline Neurol Sci Neurology neuromuscular Neuropathol normal occur onset pathological patients percent periodic paralysis plasma polymyositis potassium protein receptor reported serum CK skeletal muscle studies symptoms syndrome therapy tients tion type 1 fibers ultrastructural vacuoles viral virus X-linked