Aldo Quattrone
Aldo Quattrone
Verified email at unicz.it
Title
Cited by
Cited by
Year
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
S ZŘchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ...
Nature genetics 36 (5), 449-451, 2004
15102004
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
13952009
Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease
DM Maraganore, M De Andrade, A Elbaz, MJ Farrer, JP Ioannidis, ...
Jama 296 (6), 661-670, 2006
5132006
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
A Bolino, M Muglia, FL Conforti, E LeGuern, MAM Salih, DM Georgiou, ...
Nature genetics 25 (1), 17-19, 2000
5022000
The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy
M De Fusco, A Becchetti, A Patrignani, G Annesi, A Gambardella, ...
Nature genetics 26 (3), 275-276, 2000
5002000
The challenge of mapping the human connectome based on diffusion tractography
KH Maier-Hein, PF Neher, JC Houde, MA C˘tÚ, E Garyfallidis, J Zhong, ...
Nature communications 8 (1), 1-13, 2017
3852017
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
B Jones, EL Jones, SA Bonney, HN Patel, AR Mensenkamp, ...
Nature genetics 34 (1), 29-31, 2003
3642003
MR Imaging Index for Differentiation of Progressive Supranuclear Palsy from Parkinson Disease and the Parkinson Variant of Multiple System Atrophy1
A Quattrone, G Nicoletti, D Messina, F Fera, F Condino, P Pugliese, ...
Radiology 246 (1), 214-221, 2008
2922008
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ...
JAMA neurology 70 (6), 727-735, 2013
2852013
Manometry combined with cervical puncture in idiopathic intracranial hypertension
JO King, PJ Mitchell, KR Thomson, BM Tress
Neurology 58 (1), 26-30, 2002
2762002
UCHL1 is a Parkinson's disease susceptibility gene
DM Maraganore, TG Lesnick, A Elbaz, MC Chartier‐Harlin, T Gasser, ...
Annals of neurology 55 (4), 512-521, 2004
2742004
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ...
The Lancet Neurology 10 (10), 898-908, 2011
2312011
Apparent diffusion coefficient measurements of the middle cerebellar peduncle differentiate the Parkinson variant of MSA from Parkinson's disease and progressive supranuclear palsy
G Nicoletti, R Lodi, F Condino, C Tonon, F Fera, E Malucelli, D Manners, ...
Brain 129 (10), 2679-2687, 2006
2182006
Quetiapine and clozapine in parkinsonian patients with dopaminergic psychosis
L Morgante, A Epifanio, E Spina, M Zappia, AE Di Rosa, R Marconi, ...
Clinical neuropharmacology 27 (4), 153-156, 2004
2162004
Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial
D Pareyson, MM Reilly, A Schenone, GM Fabrizi, T Cavallaro, L Santoro, ...
The Lancet Neurology 10 (4), 320-328, 2011
2052011
Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early‐Onset Parkinsonism
M Quadri, M Fang, M Picillo, S Olgiati, GJ Breedveld, J Graafland, B Wu, ...
Human mutation 34 (9), 1208-1215, 2013
2012013
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study
M Zappia, G Annesi, G Nicoletti, G Arabia, F Annesi, D Messina, ...
Archives of neurology 62 (4), 601-605, 2005
2012005
Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivity
L Passamonti, F Fera, A Magariello, A Cerasa, MC Gioia, M Muglia, ...
Biological psychiatry 59 (4), 334-340, 2006
1862006
Identification of an Nav1. 1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures
M Mantegazza, A Gambardella, R Rusconi, E Schiavon, F Annesi, ...
Proceedings of the National Academy of Sciences 102 (50), 18177-18182, 2005
1862005
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
A Chi˛, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ...
Brain 135 (3), 784-793, 2012
1832012
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