Nerve ultrasound depicts peripheral nerve enlargement in patients with genetically distinct Charcot-Marie-Tooth disease-Reference-Cited by-同舟云学术

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Nerve ultrasound depicts peripheral nerve enlargement in patients with genetically distinct Charcot-Marie-Tooth disease

Published:2014-08-04 Issue:4 Volume:86 Page:378-384
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Noto Yu-ichi,Shiga Kensuke,Tsuji Yukiko,Mizuta Ikuko,Higuchi Yujiro,Hashiguchi Akihiro,Takashima Hiroshi,Nakagawa Masanori,Mizuno Toshiki

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference27 articles.

1. The clinical features of hereditary motor and sensory neuropathy types I and II;Harding;Brain,1980

2. CMT1X phenotypes represent loss of GJB1 gene function;Shy;Neurology,2007

3. Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing;Murphy;J Neurol Neurosurg Psychiatry,2012

4. Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients;Hattori;Brain,2003

5. Ultrasound of radial, ulnar, median, and sciatic nerves in healthy subjects and patients with hereditary motor and sensory neuropathies;Heinemeyer;Ultrasound Med Biol,1999

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2. A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian Patient;Journal of Neuromuscular Diseases;2024-01-02

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4. Evaluation of the median nerve by shear wave elastography in patients with Charcot–Marie–Tooth disease type 1A;Medical Ultrasonography;2023-06-26

5. Arg953* mutation in Periaxin causes CMT4F without nerve hypertrophy on ultrasound imaging: A case report and review of the literature;Clinical Neurophysiology;2023-03

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