Ultrastructural Distribution of PMP22 in Charcot-Marie-Tooth Disease Type 1A-Reference-Cited by-同舟云学术

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Ultrastructural Distribution of PMP22 in Charcot-Marie-Tooth Disease Type 1A

Published:1996-03 Issue:3 Volume:55 Page:290-299
ISSN:0022-3069
Container-title:Journal of Neuropathology and Experimental Neurology
language:en
Short-container-title:Journal of Neuropathology and Experimental Neurology

Author:

Haney Carol,Snipes G. Jackson,Shooter Eric M.,Suter Ueli,Garcia Carlos,Griffin John W.,Trapp Bruce D.

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://academic.oup.com/jnen/article-pdf/55/3/290/8134568/55-3-290.pdf

Cited by 58 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. A phase 1/2a, open label study to evaluate the safety and efficacy of a plasmid DNA encoding human hepatocyte growth factor in patients with Charcot-Marie-Tooth disease 1A;2024-06-14

2. Dosage effects of PMP22 on nonmyelinating Schwann cells in hereditary neuropathy with liability to pressure palsies;Neuromuscular Disorders;2022-06

3. Colocalization Analysis of Peripheral Myelin Protein-22 and Lamin-B1 in the Schwann Cell Nuclei of Wt and TrJ Mice;Biomolecules;2022-03-16

4. Neuropatie ereditarie da ipersensibilità alla pressione (neuropatia tomaculare o allantoidea);EMC - Neurologia;2018-04

5. A dual role for Integrin α6β4 in modulating hereditary neuropathy with liability to pressure palsies;Journal of Neurochemistry;2018-02-13

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