Charcot-Marie-Tooth disease: Genetic and clinical spectrum in a Spanish clinical series-Reference-Cited by-同舟云学术

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Charcot-Marie-Tooth disease: Genetic and clinical spectrum in a Spanish clinical series

Published:2013-09-27 Issue:18 Volume:81 Page:1617-1625
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Sivera R.,Sevilla T.,Vilchez J. J.,Martinez-Rubio D.,Chumillas M. J.,Vazquez J. F.,Muelas N.,Bataller L.,Millan J. M.,Palau F.,Espinos C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 118 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. Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy;Journal of Neurology, Neurosurgery & Psychiatry;2024-06-05

2. Genetic and clinical profile of 15 Chinese families with GDAP1‐related Charcot–Marie–Tooth disease and identification of H256R as a frequent mutation;Journal of the Peripheral Nervous System;2024-05-05

3. Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth disease;Neurología (English Edition);2024-03

4. Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian children;Journal of the Peripheral Nervous System;2024-02-20

5. Neurofilaments in health and Charcot-Marie-Tooth disease;Frontiers in Cell and Developmental Biology;2023-12-18

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