michelangelo mancuso
michelangelo mancuso
Neurological Clinic, AOUP & University of Pisa, Italy
Verified email at ao-pisa.toscana.it
TitleCited byYear
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
D Harold, R Abraham, P Hollingworth, R Sims, A Gerrish, ML Hamshere, ...
Nature genetics 41 (10), 1088, 2009
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452, 2013
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429, 2011
Mitochondrial diseases
S DiMauro
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1658 (1-2), 80-88, 2004
APOE and Alzheimer disease: a major gene with semi-dominant inheritance
E Genin, D Hannequin, D Wallon, K Sleegers, M Hiltunen, O Combarros, ...
Molecular psychiatry 16 (9), 903, 2011
Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer’s disease
F Bosetti, F Brizzi, S Barogi, M Mancuso, G Siciliano, EA Tendi, L Murri, ...
Neurobiology of aging 23 (3), 371-376, 2002
European Alzheimer’s Disease Initiative Investigators. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer’s disease
JC Lambert, S Heath, G Even, D Campion, K Sleegers, M Hiltunen, ...
Nat Genet 41 (10), 1094-1099, 2009
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)
G Meola, V Sansone, D Perani, S Scarone, S Cappa, C Dragoni, ...
Neuromuscular Disorders 13 (10), 813-821, 2003
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373, 2017
Early‐onset familial parkinsonism due to POLG mutations
G Davidzon, P Greene, M Mancuso, KJ Klos, JE Ahlskog, M Hirano, ...
Annals of Neurology: Official Journal of the American Neurological†…, 2006
Mitochondrial dysfunction, oxidative stress and neurodegeneration
M Mancuso, F Coppede, L Migliore, G Siciliano, L Murri
Journal of Alzheimer's Disease 10 (1), 59-73, 2006
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
L Corrado, R Del Bo, B Castellotti, A Ratti, C Cereda, S Penco, G Sorarý, ...
Journal of medical genetics 47 (3), 190-194, 2010
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA
M Mancuso, L Salviati, S Sacconi, D Otaegui, P Camano, A Marina, ...
Neurology 59 (8), 1197-1202, 2002
Mitochondria and neurodegeneration
L Petrozzi, G Ricci, NJ Giglioli, G Siciliano, M Mancuso
Bioscience reports 27 (1-3), 87-104, 2007
European Alzheimer’s Disease Initiative (EADI); Genetic and Environmental Risk in Alzheimer’s Disease; Alzheimer’s Disease Genetic Consortium; Cohorts for Heart and Aging†…
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nat Genet 45 (12), 1452-1458, 2013
Mitochondrial DNA depletion and dGK gene mutations
L Salviati, S Sacconi, M Mancuso, D Otaegui, P Camano, A Marina, ...
Annals of neurology 52 (3), 311-317, 2002
Coenzyme Q10 in neuromuscular and neurodegenerative disorders
M Mancuso, D Orsucci, L Volpi, V Calsolaro, G Siciliano
Current drug targets 11 (1), 111-121, 2010
POLG mutations and Alpers syndrome
G Davidzon, M Mancuso, S Ferraris, C Quinzii, M Hirano, HL Peters, ...
Annals of Neurology: Official Journal of the American Neurological†…, 2005
Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights
M Mancuso, G Davidzon, RM Kurlan, R Tawil, E Bonilla, S Di Mauro, ...
Journal of Neuropathology & Experimental Neurology 64 (4), 280-294, 2005
Phenotypic heterogeneity of the 8344A> G mtDNA “MERRF” mutation
M Mancuso, D Orsucci, C Angelini, E Bertini, V Carelli, GP Comi, C Minetti, ...
Neurology 80 (22), 2049-2054, 2013
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