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European Journal of Neurology|August 16, 2012
EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementiaS Sorbi, J Hort, T Erkinjuntti, et al.Annals of Neurology|December 16, 2000
Pick's disease is associated with mutations in the tau geneS Pickering-Brown, M Baker, S H Yen, et al.European Journal of Neurology|September 29, 2023
Mutations in alpha-B-crystallin cause autosomal dominant axonal Charcot-Marie-Tooth disease with congenital cataractsAndrea Cortese, Riccardo Currò, Riccardo Ronco, et al.Dementia and Geriatric Cognitive Disorders|August 7, 1999
Molecular genetic characterisation of frontotemporal dementia on chromosome 3A Ashworth, S Lloyd, J Brown, et al.Neurology|May 25, 2021
MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1AHongge Wang, Matthew Davison, Kathryn Wang, et al.Neurology|August 4, 2017
Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)Francis B Panosyan, Matilde Laura, Alexander M Rossor, et al.Journal of the Peripheral Nervous System : JPNS|July 15, 2026
VRK1-Related Motor Neuropathy With Upper Motor Neuron Signs and Selective Muscle InvolvementManoella Guerra de Albuquerque Bueno, Diogo Fernandes Dos Santos, Alexander M Rossor, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testingSinead M Murphy, Matilde Laura, Katherine Fawcett, et al.Plos Genetics|November 9, 2022
A new mouse model of Charcot-Marie-Tooth 2J neuropathy replicates human axonopathy and suggest alteration in axo-glia communicationGhjuvan'Ghjacumu Shackleford, Leandro N Marziali, Yo Sasaki, 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.Pageof 15