Clinical predominance of proximal upper limb weakness in CMT1A syndrome-Reference-Cited by-同舟云学术

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Clinical predominance of proximal upper limb weakness in CMT1A syndrome

Published:2000 Issue:8 Volume:23 Page:1243-1249
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Auer-Grumbach Michaela,Wagner Klaus,Strasser-Fuchs Siegrid,L�scher Wolfgang N.,Fazekas Franz,Millner Michael,Hartung Hans-Peter

Publisher

Wiley

Subject

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

Reference27 articles.

1. Electromyography in clinical practice. 3rd ed. New York: Churchill Livingstone; 1998.

2. Roussy–Lévy syndrome is a phenotypic variant of Charcot–Marie–Tooth syndrome IA associated with a duplication on chromosome 17p11.2

3. Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

4. Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

5. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

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2. A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy;Chinese Medical Journal;2018-09-20

3. Ulnar Nerve Tendon Transfers for Pinch;Hand Clinics;2016-08

4. Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for “double trouble” overlapping syndromes;BMC Medical Genetics;2013-09-16

5. Charcot-Marie-Tooth Diseases;Neuromuscular Disorders in Clinical Practice;2013-04-26

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