The devastating combination of Charcot-Marie-Tooth disease and facioscapulohumeral muscular dystrophy-Reference-Cited by-同舟云学术

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The devastating combination of Charcot-Marie-Tooth disease and facioscapulohumeral muscular dystrophy

Published:1998-06 Issue:6 Volume:21 Page:788-791
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

B�tefisch Cathrin M.,Lang David F.,Gutmann Ludwig

Publisher

Wiley

Subject

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

Reference20 articles.

1. : Diseases of skeletal muscle, in (eds): Pathology of Skeletal Muscle, 1st ed. New York, Churchill Livingstone, New York, 1984, pp 507-508.

2. : Hereditary motor and sensory neuropathies, in (eds): Peripheral Neuropathy, 3rd ed. Philadelphia, Saunders, 1993, vol 2, p 11026.

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unveiling a Rare Coexistence: Duchenne Muscular Dystrophy with Charcot–Marie–Tooth Disease Type 1A Presentation;Annals of Indian Academy of Neurology;2024-02-28

2. Charcot-Marie-Tooth Disease Type 1A Diagnosed Based on Abnormalities in a Nerve Conduction Study in a Patient with Myotonic Dystrophy Type 1: A Case Report;Jouranl of Korean Association of EMG Electrodiagnostic Medicine;2018-12

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

4. Coincidence of hereditary motor and sensory neuropathy type 1A and limb lumbo-muscular dystrophy type 2A;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2018

5. Towards a functional pathology of hereditary neuropathies;Acta Neuropathologica;2016-11-28

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