The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Neurology (clinical),Neurology,Sensory Systems
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4. Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth disease;Bergamin;Neuromolecular Med,2014
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1. Myelin protein zero mutation‐related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort;Brain Pathology;2023-08-15
2. Evaluation of the median nerve by shear wave elastography in patients with Charcot–Marie–Tooth disease type 1A;Medical Ultrasonography;2023-06-26
3. Arg953* mutation in Periaxin causes CMT4F without nerve hypertrophy on ultrasound imaging: A case report and review of the literature;Clinical Neurophysiology;2023-03
4. Nerve Sonography in Charcot–Marie–Tooth Disease: A Systematic Review and Meta-analysis of 6061 Measured Nerves;Ultrasound in Medicine & Biology;2022-08
5. Clinicopathological features in two families with MARS ‐related Charcot–Marie–Tooth disease;Neuropathology;2022-06-20
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