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Journal of Neurology, Neurosurgery, and Psychiatry|August 3, 2023
Nutritional peripheral neuropathiesCaroline Kramarz, Elaine Murphy, Mary M Reilly, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 27, 2011
The distal hereditary motor neuropathiesAlexander M Rossor, Bernadett Kalmar, Linda Greensmith, et al.Practical Neurology|April 23, 2015
A practical approach to the genetic neuropathiesAlexander M Rossor, Matthew R B Evans, Mary M ReillyNature Reviews. Neurology|September 11, 2013
Clinical implications of genetic advances in Charcot-Marie-Tooth diseaseAlexander M Rossor, James M Polke, Henry Houlden, et al.European Journal of Neurology|February 10, 2025
Heterozygous PNPT1 Variants Cause a Sensory Ataxic NeuropathySaif Haddad, Christopher J Record, Eleanor Self, et al.Neurology|February 1, 2019
TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMNAlexander M Rossor, Zane Jaunmuktane, Martin N Rossor, et al.Practical Neurology|January 2, 2019
Diagnosis of amyloid neuropathyMahima Kapoor, Alexander M Rossor, Zane Jaunmuktane, et al.Journal of the Peripheral Nervous System : JPNS|December 1, 2025
ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren SyndromeSaif Haddad, Roy Poh, Jason Hehir, et al.Journal of the Peripheral Nervous System : JPNS|June 3, 2026
Health Equality and Socioeconomic Impact of Hereditary Sensory Neuropathy Type 1 (HSN1) in the UKCaroline Kramarz, Lodina Recica, Jasper Morrow, et al.Muscle & Nerve|March 26, 2016
Plasma neurofilament heavy chain is not a useful biomarker in Charcot-Marie-Tooth diseaseAlexander M Rossor, Ching-Hua Lu, Axel Petzold, et al.Pageof 32