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Neurology|June 28, 2023
Association of Body Mass Index With Disease Progression in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Kayla M D Cornett, Sarah P Garnett, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2023
Quantitative MRI outcome measures in CMT1A using automated lower limb muscle segmentationLuke F O'Donnell, Menelaos Pipis, John S Thornton, et al.
Muscle & Nerve|July 23, 2016
Content validity of symptom-based measures for diabetic, chemotherapy, and HIV peripheral neuropathyJennifer S Gewandter, Laurie Burke, Guido Cavaletti, et al.
American Journal of Human Genetics|September 6, 2014
Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathyDavid N Herrmann, Rita Horvath, Janet E Sowden, et al.
Annals of Clinical and Translational Neurology|August 8, 2020
Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedSKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Annals of Neurology|August 11, 2017
Natural history of Charcot-Marie-Tooth disease during childhoodKayla M D Cornett, Manoj P Menezes, Rosemary R Shy, et al.
Muscle & Nerve|June 21, 2017
Prevalence and orthopedic management of foot and ankle deformities in Charcot-Marie-Tooth diseaseMatilde Laurá, Dishan Singh, Gita Ramdharry, et al.
Brain : a Journal of Neurology|June 25, 2024
TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestationsGage P Kosmanopoulos, Jack K Donohue, Maya Hoke, et al.
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