A Rossor
A Rossor
Unknown affiliation
Verified email at ucl.ac.uk
Cited by
Cited by
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease
D Chan, NC Fox, RI Scahill, WR Crum, JL Whitwell, G Leschziner, ...
Annals of neurology 49 (4), 433-442, 2001
Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing
SM Murphy, M Laura, K Fawcett, A Pandraud, YT Liu, GL Davidson, ...
Journal of Neurology, Neurosurgery & Psychiatry 83 (7), 706-710, 2012
Clinical implications of genetic advances in Charcot–Marie–Tooth disease
AM Rossor, JM Polke, H Houlden, MM Reilly
Nature Reviews Neurology 9 (10), 562, 2013
The distal hereditary motor neuropathies
AM Rossor, B Kalmar, L Greensmith, MM Reilly
Journal of Neurology, Neurosurgery & Psychiatry 83 (1), 6-14, 2012
Intracranial volume and Alzheimer disease: evidence against the cerebral reserve hypothesis
R Jenkins, NC Fox, AM Rossor, RJ Harvey, MN Rossor
Archives of neurology 57 (2), 220-224, 2000
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia
EC Oates, AM Rossor, M Hafezparast, M Gonzalez, F Speziani, ...
The American Journal of Human Genetics 92 (6), 965-973, 2013
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy
M Scoto, AM Rossor, MB Harms, S Cirak, M Calissano, S Robb, ...
Neurology 84 (7), 668-679, 2015
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia
A Cortese, R Simone, R Sullivan, J Vandrovcova, H Tariq, WY Yau, ...
Nature genetics 51 (4), 649-658, 2019
A practical approach to the genetic neuropathies
AM Rossor, MRB Evans, MM Reilly
Practical neurology 15 (3), 187-198, 2015
Recent advances in the genetic neuropathies
AM Rossor, PJ Tomaselli, MM Reilly
Current opinion in neurology 29 (5), 537, 2016
BAG3 mutations: another cause of giant axonal neuropathy
F Jaffer, SM Murphy, M Scoto, E Healy, AM Rossor, S Brandner, ...
Journal of the Peripheral Nervous System 17 (2), 210-216, 2012
Plasma neurofilament light chain concentration in the inherited peripheral neuropathies
Å Sandelius, H Zetterberg, K Blennow, R Adiutori, A Malaspina, M Laura, ...
Neurology 90 (6), e518-e524, 2018
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2
AM Rossor, EC Oates, HK Salter, Y Liu, SM Murphy, R Schule, ...
Brain 138 (2), 293-310, 2015
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies
E Burnor, L Yang, H Zhou, KR Patterson, C Quinn, MM Reilly, AM Rossor, ...
Neurology 90 (1), e31-e38, 2018
Clinical and genetic characterization of leukoencephalopathies in adults
DS Lynch, A Rodrigues Brandão de Paiva, WJ Zhang, E Bugiardini, ...
Brain 140 (5), 1204-1211, 2017
Left ventricular apical ballooning (takotsubo cardiomyopathy) in thyrotoxicosis
AM Rossor, SHS Pearce, PC Adams
Thyroid 17 (2), 181-182, 2007
A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance
CJ Sumner, C d’Ydewalle, J Wooley, KA Fawcett, D Hernandez, ...
The American Journal of Human Genetics 93 (5), 976-983, 2013
Rapidly progressive asymmetrical weakness in Charcot–Marie–Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathy
E Cottenie, MP Menezes, AM Rossor, JM Morrow, TA Yousry, DJ Dick, ...
Neuromuscular Disorders 23 (5), 399-403, 2013
Axonal transport and neurological disease
JN Sleigh, AM Rossor, AD Fellows, AP Tosolini, G Schiavo
Nature Reviews Neurology, 1-13, 2019
Peripheral neuropathy in complex inherited diseases: an approach to diagnosis
AM Rossor, AS Carr, H Devine, H Chandrashekar, AL Pelayo-Negro, ...
Journal of Neurology, Neurosurgery & Psychiatry 88 (10), 846-863, 2017
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