The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies part 3. Clinical, electrophysiological and pathological correlations

Journal of the Neurological Sciences

Volumn 32, Issue 1, 1977, Pages 123-136

  Bradley, W G ^a,b   Madrid, R ^a,b   Davis, C J F ^a,b  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b NEWCASTLE GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; MAJOR CLINICAL STUDY; MOTOR NERVE CONDUCTION;

ADOLESCENT; ADULT; AGE FACTORS; AGED; AXONS; CHILD; DEMYELINATING DISEASES; FEMALE; HUMAN; MALE; MEDIAN NERVE; MIDDLE AGE; MUSCULAR ATROPHY; MYELIN SHEATH; NEURAL CONDUCTION; SYNDROME;

EID: 0017374733     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-510X(77)90043-0     Document Type: Article

References (16)

1. Electromyographic studies in peroneal muscular atrophy — Charcot-Marie-Tooth disease
2. Peroneal muscular atrophy and related disorders, Part 2 (Histological findings in sural nerves)
3. Peroneal muscular atrophy and related disorders, Part 1 (Clinical manifestations as related to biopsy findings, nerve conduction and electromyography)
4. Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory and autonomic neurons
5. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy, Part 1 (Neurologic, genetic and electrophysiological findings in hereditary polyneuropathies)
6. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy, Part 2 (Neurologic, genetic and electrophysiological findings in various neuronal degenerations)
7. Charcot-Marie-Tooth disease — nerve conduction and clinical studies of a large kinship
8. Nerve conduction studies in Charcot-Marie-Tooth disease
9. The peroneal muscular atrophy syndrome — Clinical, genetic, electrophysiological and nerve biopsy studies, Part 2 (Observations on pathological changes in sural nerve biopsies)
10. Nerve conduction and other studies in families with Charcot-Marie-Tooth disease
11. Wide spectrum of motor conduction velocity in Charcot-Marie-Tooth disease — An anatomico-physiological interpretation
12. Motor nerve conduction velocity in peroneal muscular atrophy — Evidence for genetic heterogeneity
13. Hereditary motor and sensory polyneuropathy (Peroneal muscular atrophy)