Tamas Revesz
Tamas Revesz
Emeritus Professor of Neuropathology, UCL Queen Square Institute of Neurology, Univ Coll London
Verified email at
Cited by
Cited by
Second consensus statement on the diagnosis of multiple system atrophy
S Gilman, GK Wenning, PA Low, DJ Brooks, CJ Mathias, JQ Trojanowski, ...
Neurology 71 (9), 670-676, 2008
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
JY Li, E Englund, JL Holton, D Soulet, P Hagell, AJ Lees, T Lashley, ...
Nature medicine 14 (5), 501-503, 2008
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ...
Acta neuropathologica 119 (1), 1-4, 2010
Cortical lesions in multiple sclerosis
D Kidd, F Barkhof, R McConnell, PR Algra, IV Allen, T Revesz
Brain 122 (1), 17-26, 1999
A common LRRK2 mutation in idiopathic Parkinson's disease
WP Gilks, PM Abou-Sleiman, S Gandhi, S Jain, A Singleton, AJ Lees, ...
The Lancet 365 (9457), 415-416, 2005
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
DR Williams, R de Silva, DC Paviour, A Pittman, HC Watt, L Kilford, ...
Brain 128 (6), 1247-1258, 2005
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
J Neumann, J Bras, E Deas, SS O'Sullivan, L Parkkinen, RH Lachmann, ...
Brain 132 (7), 1783-1794, 2009
Lewy-and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?
Y Compta, L Parkkinen, SS O'Sullivan, J Vandrovcova, JL Holton, ...
Brain 134 (5), 1493-1505, 2011
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
R Bandopadhyay, AE Kingsbury, MR Cookson, AR Reid, IM Evans, ...
Brain 127 (2), 420-430, 2004
A stop-codon mutation in the BRI gene associated with familial British dementia
R Vidal, B Frangione, A Rostagno, S Mead, T Révész, G Plant, J Ghiso
Nature 399 (6738), 776-781, 1999
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, P Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699-705, 2011
A clinico-pathological study of subtypes in Parkinson's disease
M Selikhova, DR Williams, PA Kempster, JL Holton, T Revesz, AJ Lees
Brain 132 (11), 2947-2957, 2009
The heritability and genetics of frontotemporal lobar degeneration
JD Rohrer, R Guerreiro, J Vandrovcova, J Uphill, D Reiman, J Beck, ...
Neurology 73 (18), 1451-1456, 2009
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations
T Ozawa, D Paviour, NP Quinn, KA Josephs, H Sangha, L Kilford, ...
Brain 127 (12), 2657-2671, 2004
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ...
Acta neuropathologica 117 (1), 15-18, 2009
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
CJ Mahoney, J Beck, JD Rohrer, T Lashley, K Mok, T Shakespeare, ...
Brain 135 (3), 736-750, 2012
Relationships between age and late progression of Parkinson’s disease: a clinico-pathological study
PA Kempster, SS O’Sullivan, JL Holton, T Revesz, AJ Lees
Brain 133 (6), 1755-1762, 2010
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy?
AP Kiely, YT Asi, E Kara, P Limousin, H Ling, P Lewis, C Proukakis, ...
Acta neuropathologica 125 (5), 753-769, 2013
Clinicopathological investigation of vascular parkinsonism, including clinical criteria for diagnosis
JCM Zijlmans, SE Daniel, AJ Hughes, T Révész, AJ Lees
Movement disorders: official journal of the Movement Disorder Society 19 (6 …, 2004
Neuropathology underlying clinical variability in patients with synucleinopathies
GM Halliday, JL Holton, T Revesz, DW Dickson
Acta neuropathologica 122 (2), 187-204, 2011
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