Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation-Reference-Cited by-同舟云学术

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Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation

Published:1998-08-01 Issue:8 Volume:121 Page:1451-1458
ISSN:1460-2156
Container-title:Brain
language:
Short-container-title:

Author:

Lenssen P.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/121/8/1451/17862263/1211451.pdf

Cited by 83 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. Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion;Neurología (English Edition);2021-04

2. New evidence for secondary axonal degeneration in demyelinating neuropathies;Neuroscience Letters;2021-01

3. An 18-year-old man of hereditary neuropathy with liability to pressure palsies presenting with bilateral brachial plexopathy during military training;Rinsho Shinkeigaku;2021

4. A New Point Mutation in the PMP22 Gene in a Family Suffering From Atypical HNPP;Journal of Neuromuscular Diseases;2020-09-18

5. Yield of the PMP22 deletion analysis in patients with compression neuropathies;Journal of Neurology;2020-07-08

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