A Schapira
A Schapira
University College London, Royal Free
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, K Abdelmohsen, A Abe, MJ Abedin, H Abeliovich, ...
Autophagy 12 (1), 1-222, 2016
63962016
Non-motor symptoms of Parkinson's disease: diagnosis and management
KR Chaudhuri, DG Healy, AHV Schapira
The Lancet Neurology 5 (3), 235-245, 2006
23382006
Mitochondrial complex I deficiency in Parkinson's disease
AHV Schapira, JM Cooper, D Dexter, JB Clark, P Jenner, CD Marsden
Journal of neurochemistry 54 (3), 823-827, 1990
19891990
Mitochondrial complex I deficiency in Parkinson's disease
AHV Schapira, JM Cooper, D Dexter, P Jenner, JB Clark, CD Marsden
The Lancet 333 (8649), 1269, 1989
13791989
Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide: implications for neurodegenerative diseases
MWJ Cleeter, JM Cooper, VM Darley-Usmar, S Moncada, AHV Schapira
FEBS letters 345 (1), 50-54, 1994
13761994
Non-motor symptoms of Parkinson's disease: dopaminergic pathophysiology and treatment
KR Chaudhuri, AHV Schapira
The Lancet Neurology 8 (5), 464-474, 2009
13562009
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ...
The Lancet Neurology 7 (7), 583-590, 2008
10642008
Mitochondrial disease
AHV Schapira
The Lancet 368 (9529), 70-82, 2006
10482006
International multicenter pilot study of the first comprehensive self‐completed nonmotor symptoms questionnaire for Parkinson's disease: the NMSQuest study
KR Chaudhuri, P Martinez‐Martin, AHV Schapira, F Stocchi, K Sethi, ...
Movement disorders: official journal of the Movement Disorder Society 21 (7 …, 2006
8402006
Mitochondria in the aetiology and pathogenesis of Parkinson's disease
AHV Schapira
The Lancet Neurology 7 (1), 97-109, 2008
7802008
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy
ME Gegg, JM Cooper, KY Chau, M Rojo, AHV Schapira, JW Taanman
Human molecular genetics 19 (24), 4861-4870, 2010
7302010
Mitochondrial defect in Huntington's disease caudate nucleus
M Gu, MT Gash, VM Mann, F Javoy‐Agid, JM Cooper, AHV Schapira
Annals of Neurology: Official Journal of the American Neurological …, 1996
7301996
Missing pieces in the Parkinson's disease puzzle
JA Obeso, MC Rodriguez-Oroz, CG Goetz, C Marin, JH Kordower, ...
Nature medicine 16 (6), 653-661, 2010
7182010
Anatomic and Disease Specificity of NADH CoQ1 Reductase (Complex I) Deficiency in Parkinson's Disease
AHV Schapira, VM Mann, JM Cooper, D Dexter, SE Daniel, P Jenner, ...
Journal of neurochemistry 55 (6), 2142-2145, 1990
7171990
Mitochondrial encephalomyopathies
S DiMauro, CT Moraes
Archives of Neurology 50 (11), 1197-1208, 1993
6441993
The metric properties of a novel non‐motor symptoms scale for Parkinson's disease: results from an international pilot study
KR Chaudhuri, P Martinez‐Martin, RG Brown, K Sethi, F Stocchi, P Odin, ...
Movement disorders 22 (13), 1901-1911, 2007
6252007
Oxidative stress as a cause of nigral cell death in Parkinson's disease and incidental Lewy body disease
P Jenner, DT Dexter, J Sian, AHV Schapira, CD Marsden
Annals of Neurology: Official Journal of the American Neurological …, 1992
5681992
Etiology and pathogenesis of Parkinson's disease
AH Schapira, P Jenner
Movement disorders 26 (6), 1049-1055, 2011
5312011
Prevalence of nonmotor symptoms in Parkinson's disease in an international setting; study using nonmotor symptoms questionnaire in 545 patients
P Martinez‐Martin, AHV Schapira, F Stocchi, K Sethi, P Odin, G MacPhee, ...
Movement disorders: official journal of the Movement Disorder Society 22 (11 …, 2007
5312007
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
CAD Smith, CR Wolf, AC Gough, NK Spurr, PN Leigh, BA Summers, ...
The Lancet 339 (8806), 1375-1377, 1992
4981992
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