Hereditary distal spinal muscular atrophy: A report on 34 cases and a review of the literature☆
References (25)
- et al.
Benign spinal muscular atrophy arising in childhood and adolescence
J. neurol. Sci.
(1967) - et al.
Hereditary motor peripheral neuropathy affecting the arms
J. neurol. Sci.
(1976) - et al.
Chronic neurogenic muscle atrophies of infancy Their nosological relationship with Werdnig-Hoffmann's disease
J. neurol. Sci.
(1966) - et al.
Chronic spinal muscular atrophy in adults, Part 1 (The Kugelberg-Welander syndrome)
J. neurol. Sci.
(1969) - et al.
Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome
Acta neurol. scand.
(1978) - et al.
Peroneal muscular atrophy and related disorders, Part 1 (Clinical manifestations as related with biopsy findings, nerve conduction and electromyography)
Brain
(1976) - et al.
The peroneal muscular atrophy syndrome — Clinical, genetic, electrophysiological and nerve biopsy studies
J. Génét. hum.
(1978) - et al.
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy, Part 1 (Neurologic, genetic and electrophysiological findings in hereditary polyneuropathy)
Arch. Neurol. (Chic.)
(1968) - et al.
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy, Part 2 (Neurologic, genetic and electrophysiological findings in various neuronal degenerations)
Arch. Neurol. (Chic.)
(1968) Review: The nosology of the spinal muscular atrophies
J. med. Genet.
(1971)
Methodology in Medical Genetics
Neurogenic atrophy simulating facioscapulohumeral dystrophy
Arch. Neurol. (Chic.)
(1967)
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Financial support from the Friedreich's Ataxia Group is gratefully acknowledged.
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Present address: MRC Clinical Genetics Unit, Institute of Child Health, London, Great Britain.
Copyright © 1980 Published by Elsevier B.V.