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Brain : a Journal of Neurology|November 27, 2018
Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 29, 2014
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisV Fridman, B Bundy, M M Reilly, et al.Neurology|October 15, 2020
Idiopathic distal sensory polyneuropathy: ACTTION diagnostic criteriaRoy Freeman, Jennifer S Gewandter, Catharina G Faber, et al.Journal of Clinical Neuromuscular Disease|December 17, 2008
Diagnosis and Treatment of Chronic Immune-mediated NeuropathiesNorman Latov, Kenneth C Gorson, Thomas H Brannagan, 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.Journal of Biotechnology|February 13, 2001
Physiological responses to mixing in large scale bioreactorsS O Enfors, M Jahic, A Rozkov, 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.European Journal of Neurology|February 13, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13Alessandro Bertini, Mary M Reilly, Chiara Pisciotta, et al.Annals of Neurology|October 7, 2022
Disease Progression in Charcot-Marie-Tooth Disease Related to MPZ Mutations: A Longitudinal StudyVera Fridman, Stefan Sillau, Jacob Bockhorst, 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 33