Axonal Charcot–Marie–Tooth disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology
Reference84 articles.
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3. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.;Dyck;Arch Neurol,1968
4. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.;Dyck;Arch Neurol,1968
5. Diagnosis and new treatments in genetic neuropathies.;Reilly;J Neurol Neurosurg Psychiatry,2009
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1. TFG mutation induces haploinsufficiency and drives axonal Charcot–Marie–Tooth disease by causing neurite degeneration;CNS Neuroscience & Therapeutics;2022-08-19
2. SARM1 signaling mechanisms in the injured nervous system;Current Opinion in Neurobiology;2021-08
3. Late adult-onset Hereditary Sensory and Motor Neuropathy due to TECPR2 mutations;Revista Neurociências;2020-10-19
4. Disruption of genes associated with Charcot-Marie-Tooth type 2 lead to common behavioural, cellular and molecular defects in Caenorhabditis elegans;PLOS ONE;2020-04-15
5. Axonal Endoplasmic Reticulum Dynamics and Its Roles in Neurodegeneration;Frontiers in Neuroscience;2020-01-29
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