Disorders of Voluntary MuscleJohn Nicholas Walton |
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Page 776
... CLINICAL FEATURES OF THE MOTOR NEURONE DISEASES Whatever the cause of the muscular atrophy , the presenting clinical features are easily recognisable . The patient complains of weakness , wasting and often of sensible flickerings in the ...
... CLINICAL FEATURES OF THE MOTOR NEURONE DISEASES Whatever the cause of the muscular atrophy , the presenting clinical features are easily recognisable . The patient complains of weakness , wasting and often of sensible flickerings in the ...
Page 887
... clinical and radiological characteristics ( Spillane , Pallis and Jones , 1957 ) . The association between syringomyelia and these anomalies is well known , but more recently ( Gardner , 1965 ; Appleby , Foster , Hankinson and Hudgson ...
... clinical and radiological characteristics ( Spillane , Pallis and Jones , 1957 ) . The association between syringomyelia and these anomalies is well known , but more recently ( Gardner , 1965 ; Appleby , Foster , Hankinson and Hudgson ...
Page 1003
John Nicholas Walton. CHAPTER 28 Clinical Electromyography A. T. Richardson and D. D. Barwick INTRODUCTION TECHNIQUE OF CLINICAL ELECTROMYOGRAPHY THE PHYSIOLOGICAL BASIS OF ELECTROMYOGRAPHY The Motor Unit THE POTENTIALS STUDIED IN CLINICAL ...
John Nicholas Walton. CHAPTER 28 Clinical Electromyography A. T. Richardson and D. D. Barwick INTRODUCTION TECHNIQUE OF CLINICAL ELECTROMYOGRAPHY THE PHYSIOLOGICAL BASIS OF ELECTROMYOGRAPHY The Motor Unit THE POTENTIALS STUDIED IN CLINICAL ...
Contents
Chapter Page | 1 |
Pathological Reactions of the Skeletal Muscle Fibre in | 168 |
The Pathology of Peripheral Nerve Disease W G Bradley | 234 |
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abnormal acid Acta action activity affected Amer animals appears Arch associated axonal Biochem Biol biopsy Brain cause cells cent changes Chapter characteristic clinical condition conduction contraction creatine culture cytoplasm defect deficiency degeneration demonstrated denervation described disease disorders Duchenne early electron end-plate enzyme evidence factors Figure findings function genetic glycogen histochemical human hypothyroidism increased indicate involvement later lesions levels limb Lond membrane microscopic motor muscle fibres muscular atrophy muscular dystrophy myasthenia gravis myopathy myosin Nature nerve Neurol Neurology neuromuscular neuropathy normal nuclei observed occur onset pain paralysis pathological patients periodic peripheral nerve polymyositis possible potential present Proc produced progressive protein Psychiat rare reaction recent reported response seen sensory serum severe shown similar skeletal muscle spinal stages stimulation structure studies suggested symptoms syndrome terminal tissue tubocurarine units usually Walton weakness