Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference172 articles.
1. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
2. RELATION OF HEREDITARY PATTERN TO CLINICAL SEVERITY AS ILLUSTRATED BY PERONEAL ATROPHY
3. Widespread expression of the peripheral myelin protein-22 gene (pmp22) in neural and non-neural tissues during murine development
4. HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES. ELECTROPHYSIOLOGICAL AND HISTOPATHOLOGICAL ASPECTS
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1. X-linked Charcot Marie Tooth mutations alter CO2 sensitivity of connexin32 hemichannels;Frontiers in Cellular Neuroscience;2023-12-21
2. Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders;Heliyon;2023-09
3. Comparison of clinical and electrophysiological features of patients with hereditary neuropathy with liability to pressure palsies with or without pain;Journal of the Neurological Sciences;2020-02
4. Aminosalicylic acid reduces ER stress and Schwann cell death induced by MPZ mutations;International Journal of Molecular Medicine;2019-05-02
5. Schwann Cell and the Pathogenesis of Charcot–Marie–Tooth Disease;Advances in Experimental Medicine and Biology;2019
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