A Clinician's View of Neuromuscular Diseases |
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Page 222
... laboratory studies , 183-184 provocative factors , 183 treatment , 184 secondary , 185 Hypoparathyroidism , 180 Hypothyroidism , 179 Hypotonia , 15-16 cerebral , 201 congenital , 200-203 benign , 201 with type 1 fiber predominance , 201 ...
... laboratory studies , 183-184 provocative factors , 183 treatment , 184 secondary , 185 Hypoparathyroidism , 180 Hypothyroidism , 179 Hypotonia , 15-16 cerebral , 201 congenital , 200-203 benign , 201 with type 1 fiber predominance , 201 ...
Page 223
... laboratory studies , 78-80 pathology and etiology , 80-83 thyroid disorders and , 76 treatment , 83-87 Myasthenic crisis , 86 Myasthenic syndrome , 89-91 Myelin , 58 Myoedema , 17 , 179 Myoglobin , 173 Myoglobinuria , 159 , 162 , 164 ...
... laboratory studies , 78-80 pathology and etiology , 80-83 thyroid disorders and , 76 treatment , 83-87 Myasthenic crisis , 86 Myasthenic syndrome , 89-91 Myelin , 58 Myoedema , 17 , 179 Myoglobin , 173 Myoglobinuria , 159 , 162 , 164 ...
Page 225
... laboratory studies , 37 treatment , 38 chronic infantile , 38-41 clinical aspects , 38-40 laboratory studies , 40-41 intermediate , see Spinal muscular atrophy , chronic infantile juvenile , 41-43 clinical aspects , 41-42 differential ...
... laboratory studies , 37 treatment , 38 chronic infantile , 38-41 clinical aspects , 38-40 laboratory studies , 40-41 intermediate , see Spinal muscular atrophy , chronic infantile juvenile , 41-43 clinical aspects , 41-42 differential ...
Contents
Chapter 5 MUSCULAR DYSTROPHIES | 95 |
Chapter 6 MYOTONIA | 125 |
Chapter 7 INFLAMMATORY MYOPATHIES | 138 |
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abnormal acid activity acute appearance Arch arms associated attack become begins body carriers cause cells changes characteristic child clinical common creatine decreased deficiency demonstrate described detected develop diagnosis difficulty Duchenne's early effect elevation Engel enzyme evaluation evidence examination exercise fasciculations fibers Figure findings foot frequently function give glucose groups hand helpful illness increased inherited involved knee known Laboratory later legs less levels limb medication membrane mild motor neuron disease movement muscle biopsy muscle fibers muscular dystrophy myasthenia gravis myopathy myotonia nerve neuromuscular neuropathy normal noted noticed occur pain paralysis particularly patients perhaps period peripheral polymyositis position possible potentials present probably produced progressive proximal rare reported respiratory response rest seems seen serum severe shoulder showed side signs similar spinal muscular atrophy strength studies suggested symptoms syndrome treatment Type usually variety walk wasting weakness