Centrally involved X-linked Charcot-Marie-Tooth disease presenting as a stroke-mimic
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),Neurology (clinical)
Reference7 articles.
1. Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
2. The CNS phenotype of X-linked Charcot-Marie-Tooth disease: More than a peripheral problem
3. The Central Nervous System Phenotype of X-Linked Charcot-Marie-Tooth Disease
4. Episodic neurological dysfunction in hereditary peripheral neuropathy;Kulkarni;Ann Indian Acad Neurol,2015
5. Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease
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1. Charcot-Marie-Tooth Disease;Reference Module in Neuroscience and Biobehavioral Psychology;2024
2. Pregnancy as trigger of central nervous system dysfunction in type 1 X‐linked Charcot–Marie–Tooth disease;Muscle & Nerve;2023-08-10
3. Systematic review of CMTX1 patients with episodic neurological dysfunction;Annals of Clinical and Translational Neurology;2020-12-12
4. Recurrent episodes of reversible posterior leukoencephalopathy in three Chinese families with GJB1 mutations in X-linked Charcot-Marie-tooth type 1 disease: cases report;BMC Neurology;2019-12
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