alessandro filla
alessandro filla
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TitleCited byYear
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion
V Campuzano, L Montermini, MD Moltò, L Pianese, M Cossée, ...
Science 271 (5254), 1423-1427, 1996
Association between early-onset Parkinson's disease and mutations in the parkin gene
CB Lücking, A Dürr, V Bonifati, J Vaughan, G De Michele, T Gasser, ...
New England Journal of Medicine 342 (21), 1560-1567, 2000
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome
P Trouillas, T Takayanagi, M Hallett, RD Currier, SH Subramony, ...
Journal of the neurological sciences 145 (2), 205-211, 1997
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
G Casari, M De Fusco, S Ciarmatori, M Zeviani, M Mora, P Fernandez, ...
Cell 93 (6), 973-983, 1998
A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe
N Abbas, CB Lücking, S Ricard, A Dürr, V Bonifati, G De Michele, ...
Human molecular genetics 8 (4), 567-574, 1999
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.
A Filla, G De Michele, F Cavalcanti, L Pianese, A Monticelli, ...
American journal of human genetics 59 (3), 554, 1996
Multiple system atrophy
GK Wenning, C Colosimo, F Geser, W Poewe
The Lancet Neurology 3 (2), 93-103, 2004
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes
M Cossée, A Dürr, M Schmitt, N Dahl, P Trouillas, P Allinson, M Kostrzewa, ...
Annals of Neurology: Official Journal of the American Neurological …, 1999
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum
G Stevanin, FM Santorelli, H Azzedine, P Coutinho, J Chomilier, ...
Nature genetics 39 (3), 366, 2007
The Friedreich ataxia GAA triplet repeat: premutation and normal alleles
L Montermini, E Andermann, M Labuda, A Richter, M Pandolfo, ...
Human molecular genetics 6 (8), 1261-1266, 1997
Safety, tolerability, and efficacy of TEV-48125 for preventive treatment of high-frequency episodic migraine: a multicentre, randomised, double-blind, placebo-controlled, phase …
ME Bigal, DW Dodick, AM Rapoport, SD Silberstein, Y Ma, R Yang, ...
The Lancet Neurology 14 (11), 1081-1090, 2015
Environmental and genetic risk factors in Parkinson's disease: a case–control study in southern Italy
G De Michele, A Filla, G Volpe, V De Marco, A Gogliettino, G Ambrosio, ...
Movement disorders: official journal of the Movement Disorder Society 11 (1 …, 1996
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, ...
Neurology 71 (13), 982-989, 2008
Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
Multiple-System Atrophy Research Collaboration
New England Journal of Medicine 369 (3), 233-244, 2013
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage
A Suraweera, OJ Becherel, P Chen, N Rundle, R Woods, J Nakamura, ...
The Journal of cell biology 177 (6), 969-979, 2007
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
M Muona, SF Berkovic, LM Dibbens, KL Oliver, S Maljevic, MA Bayly, ...
Nature genetics 47 (1), 39, 2015
Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features
MT Pellecchia, R Scala, A Filla, G De Michele, C Ciacci, P Barone
Journal of Neurology, Neurosurgery & Psychiatry 66 (1), 32-35, 1999
PARK6‐linked parkinsonism occurs in several European families
EM Valente, F Brancati, A Ferraris, EA Graham, MB Davis, MMB Breteler, ...
Annals of Neurology: Official Journal of the American Neurological …, 2002
Clinical and neurological abnormalities in adult celiac disease
G Cicarelli, G Della Rocca, M Amboni, C Ciacci, G Mazzacca, A Filla, ...
Neurological Sciences 24 (5), 311-317, 2003
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24. 3
G De Michele, M De Fusco, F Cavalcanti, A Filla, R Marconi, G Volpe, ...
The American Journal of Human Genetics 63 (1), 135-139, 1998
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