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Journal of the Neurological Sciences|June 2, 2017
In-vivo reflectance confocal microscopy of Meissner's corpuscles in diabetic distal symmetric polyneuropathyPeter D Creigh, Michael P McDermott, Janet E Sowden, et al.Journal of Clinical Neuromuscular Disease|August 23, 2013
Patient identification of the symptomatic impact of charcot-marie-tooth disease type 1ANicholas E Johnson, Chad R Heatwole, Michele Ferguson, et al.Annals of Clinical and Translational Neurology|August 16, 2019
Measuring peripheral nerve involvement in Friedreich's ataxiaPeter D Creigh, Joan Mountain, Janet E Sowden, et al.Frontiers in Neurology|July 14, 2022
Accelerate Clinical Trials in Charcot-Marie-Tooth Disease (ACT-CMT): A Protocol to Address Clinical Trial Readiness in CMT1AKaty Eichinger, Janet E Sowden, Joshua Burns, et al.Neurology|November 1, 2015
Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndromeRoger G Whittaker, David N Herrmann, Boglarka Bansagi, et al.Journal of the Peripheral Nervous System : JPNS|August 27, 2020
Reliability of the Charcot-Marie-Tooth functional outcome measurePaula Bray, Kayla M D Cornett, Timothy Estilow, 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.Neurology|September 8, 2021
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Sarah P Garnett, Kayla M D Cornett, et al.American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.Brain : a Journal of Neurology|December 16, 2014
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2Alexander M Rossor, Emily C Oates, Hannah K Salter, et al.Pageof 2