Distal and scapuloperoneal distributions of muscle involvement occurring within a family with type I hereditary motor and sensory neuropathy-Reference-Cited by-同舟云学术

Distal and scapuloperoneal distributions of muscle involvement occurring within a family with type I hereditary motor and sensory neuropathy

Published:1980-09 Issue:1 Volume:224 Page:17-23
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J. Neurol.

Author:

Harding A. E.,Thomas P. K.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/BF00313203.pdf

Reference15 articles.

1. Brust JCM, Lovelace RE, Devi S (1978) Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome. Acta Neurol Scand 58: Supplement 68:1?142

2. Davidenkow S (1972) Über die neurotische Muskelatrophie Charcot-Marie. Klinisch-genetische Studien. Z ges Neurol Psychiat 107:259?320

3. Davidenkow S (1939) Scapuloperoneal amyotrophy. Arch Neurol Psychiat (Chic) 41:694?701

4. Dyck PJ, Lambert EH (1968) Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic and electrophysiologic findings in hereditary polyneuropathy. Arch Neurol (Chic) 18:603?618

5. Dyck PJ, Lambert EH (1968) Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic and electrophysiologic findings in various neuronal degenerations. Arch Neurol (Chic) 18:619?625

Cited by 21 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. Davidenkow syndrome: A phenotypic variant of hereditary neuropathy with liability to pressure palsies;Muscle & Nerve;2017-10-24

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

3. Reliability and validity of the CMT neuropathy score as a measure of disability;Neurology;2005-04-11

4. Neuropathic scapuloperoneal syndrome (Davidenkow's syndrome) with chromosome 17p11.2 deletion;Muscle & Nerve;2005

5. Hereditary Motor and Sensory Neuropathies Involving Altered Dosage or Mutation of PMP22: The CMT1A Duplication and HNPP Deletion;Peripheral Neuropathy;2005