Neuropathy progression in Charcot-Marie-Tooth disease type 1A-Reference-Cited by-同舟云学术

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Neuropathy progression in Charcot-Marie-Tooth disease type 1A

Published:2008-01-28 Issue:5 Volume:70 Page:378-383
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Shy M. E.,Chen L.,Swan E. R.,Taube R.,Krajewski K. M.,Herrmann D.,Lewis R. A.,McDermott M. P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 106 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. Clinical spectrum and frequency of Charcot–Marie–Tooth disease in Italy: Data from the National CMT Registry;European Journal of Neurology;2023-05-26

3. The systemic inhibition of the terminal complement system reduces neuroinflammation but does not improve motor function in mouse models of CMT1A with overexpressed PMP22;Current Research in Neurobiology;2023

4. Magnetic resonance imaging-based lower limb muscle evaluation in Charcot-Marie-Tooth disease type 1A patients and its correlation with clinical data;Scientific Reports;2022-10-05

5. Candidate imaging biomarkers for PMP22 ‐related inherited neuropathies;Annals of Clinical and Translational Neurology;2022-06-03

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