Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene-Reference-Cited by-同舟云学术

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Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene

Published:2002-10 Issue:7-8 Volume:12 Page:651-655
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

van de Wetering R.A.C,Gabreëls-Festen A.A.W.M,Timmerman V,Padberg G.W,Gabreëls F.J.M,Mariman E.C.M

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects;Behse;Brain,1972

2. Hereditary neuropathy with liability to pressure palsies: a clinical, electroneurophysiological and morphological study;Verhagen;J Neurol Sci,1993

3. Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion;Gouider;Neurology,1995

4. DNA deletion associated with hereditary neuropathy with liability to pressure palsies;Chance;Cell,1993

5. Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit;Pentao;Nat Genet,1992

Cited by 23 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. Pathology of the peripheral nervous system;Neuroglia;2023

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

3. Hereditary Liability to Pressure Palsies;Neuromuscular Disorders;2017-12-28

4. Hereditary Neuropathy With Liability to Pressure Palsies: Diverse Phenotypes in Childhood;Journal of Clinical Neuromuscular Disease;2016-12

5. Clinical and genetic spectra in a series of Chinese patients with Charcot–Marie–Tooth disease;Clinica Chimica Acta;2015-12

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