Initial semeiology in children with Charcot-Marie-Tooth disease 1A duplication-Reference-Cited by-同舟云学术

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Initial semeiology in children with Charcot-Marie-Tooth disease 1A duplication

Published:2002-12-06 Issue:1 Volume:27 Page:34-39
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Berciano José,García Antonio,Combarros Onofre

Funder

Fundación “La Caixa”

Fondo de Investigación Sanitaria

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference27 articles.

1. The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy;Berciano;Muscle Nerve,1989

2. Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot-Marie-Tooth disease 1A duplication;Berciano;Neuromuscul Disord,2000

3. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases;Birouk;Brain,1997

4. Dominantly inherited motor and sensory neuropathy type I. Genetic, clinical, electrophysiological and pathological features in four families;Combarros;J Neurol Sci,1986

5. Prevalence of hereditary motor and sensory neuropathy in Cantabria;Combarros;Acta Neurol Scand,1986

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4. Postural instability in Charcot-Marie-Tooth 1A disease;Gait & Posture;2016-09

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