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Neuromuscular Disorders : NMD|November 7, 2016
Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 geneAlexander M Rossor, Jasper M Morrow, James M Polke, et al.Practical Neurology|November 20, 2025
Severe lupus vasculitic neuropathyApoorva Anil Kumar, Victor Jia Wei Zhang, Carine J Moezinia, et al.Neuromuscular Disorders : NMD|November 3, 2018
IGHMBP2 mutation associated with organ-specific autonomic dysfunctionPedro J Tomaselli, Alejandro Horga, Alexander M Rossor, et al.Neurology|December 1, 1996
A multicenter double-blind study of controlled-release physostigmine for the treatment of symptoms secondary to Alzheimer's disease. Physostigmine Study GroupL J Thal, G Schwartz, M Sano, et al.Archives of Neurology|December 26, 2001
Current concepts in mild cognitive impairmentR C Petersen, R Doody, A Kurz, et al.Journal of the Peripheral Nervous System : JPNS|June 28, 2012
BAG3 mutations: another cause of giant axonal neuropathyFatima Jaffer, Sinéad M Murphy, Mariacristina Scoto, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 11, 2017
Peripheral neuropathy in complex inherited diseases: an approach to diagnosisAlexander M Rossor, Aisling S Carr, Helen Devine, et al.Journal of the Peripheral Nervous System : JPNS|June 28, 2012
A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2Alexander M Rossor, Gabrielle L Davidson, Julian Blake, et al.Neurology|January 6, 2009
Microglial activation and amyloid deposition in mild cognitive impairment: a PET studyA Okello, P Edison, H A Archer, et al.Journal of the Peripheral Nervous System : JPNS|December 22, 2023
Digenic FLNA and UCHL1 variants resulting in a complex phenotypeHelena F Pernice, Luke F O'Donnell, Alexander M Rossor, et al.Pageof 15