FILLA, ALESSANDRO

FILLA, ALESSANDRO  

DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE  

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Influence of GAA expansion size and disease duration on Central Nervous System impairment in Friedreich's Ataxia. Contribution to the understanding of the pathophysiology of the disease 1.1 Articolo in rivista 2000 Santoro, L.; Perretti, ANNA CARMELA AGNESE; Lanzillo, B.; Coppola, G.; DE JOANNA, G.; Manganelli, F.; Cocozza, Sergio; DE MICHELE, Giuseppe; Filla, Alessandro; Caruso, G.
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients 1.1 Articolo in rivista 1996 Perretti, ANNA CARMELA AGNESE; Santoro, L.; Lanzillo, B.; Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, F.; Martino, G.; Ragno, M.; Cocozza, Sergio; Caruso, G.
DNA damage induced by polyglutamine-expanded proteins. 1.1 Articolo in rivista 2003 Giuliano, P; Affaitati, A; Pizzulo, Gm; Feliciello, A; Criscuolo, C; DE MICHELE, Giuseppe; Filla, Alessandro; Avvedimento, VITTORIO ENRICO; Varrone, S.
Paroxysmal dystonia in Behcet's disease. 1.1 Articolo in rivista 1999 Pellecchia, Mt; Cuomo, T; Striano, Salvatore; Filla, Alessandro; Barone, P.
Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus 1.1 Articolo in rivista 1994 De, Michele; Filla, Alessandro; Cavalcanti, F; Varrone, Stelio
Early-onset inherited ataxia 2.1 Contributo in volume (Capitolo o Saggio) 2002 DE MICHELE, Giuseppe; Filla, Alessandro
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 1.1 Articolo in rivista 2002 Pianese, L; Busino, L; DE BIASE, I; DE CRISTOFARO, T; LO CASALE, Ms; Giuliano, P; Turano, M; Criscuolo, C; Filla, Alessandro; Varrone, Stelio; Cocozza, Sergio
Friedreich's disease. A linkage study in southern andcentral Italy. 1.1 Articolo in rivista 1994 Cavalcanti, F.; Cocozza, Sergio; Filla, Alessandro; Varrone, Stelio
Early-onset cerebellar ataxia with retained tendon reflexes 2.1 Contributo in volume (Capitolo o Saggio) 2000 Filla, Alessandro; DE MICHELE, Giuseppe
Genetic abnormalities in Friedreich's ataxia. 1.1 Articolo in rivista 1997 Filla, Alessandro; DE MICHELE, Giuseppe; Cocozza, Sergio
Effects of tartrate thyrotropin-releasing hormone treatment on serum thyrotropin, free triiodothyronine, free thyroxine and prolactin levels in patients with spinocerebellar degeneration 1.1 Articolo in rivista 1992 Merola, Bartolomeo; Colao, Annamaria; DI RENZO, GIANFRANCO MARIA LUIGI; Filla, Alessandro; G., Campanella; Lombardi, Gaetano
Ictus ischemico 2.1 Contributo in volume (Capitolo o Saggio) 2012 Filla, Alessandro; Caranci, Ferdinando; S., Peluso
Is early onset cerebellar ataxia with retained tendon reflexes identifiable by electrophysiologic and hystologic profile? A comparison with Friedreich's ataxia 1.1 Articolo in rivista 1992 Santoro, Lucio; Perretti, A.; Filla, Alessandro; DE MICHELE, Giuseppe; Lanzillo, B.; Barbieri, F.; Crisci, C.; Caruso, G.
Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity. 1.1 Articolo in rivista 1993 G., Sirugo; Cocozza, Sergio; A., Brice; F., Cavalcanti; DE MICHELE, Giuseppe; I., Dones; Filla, Alessandro; M., Koenig; D., Lorenzetti; A., Monticelli
Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data. 1.1 Articolo in rivista 2013 Jacobi, H; Reetz, K; du Montcel, St; Bauer, P; Mariotti, C; Nanetti, L; Rakowicz, M; Sulek, A; Durr, A; Charles, P; Filla, Alessandro; Antenora, A; Sch?ls, L; Schicks, J; Infante, J; Kang, Js; Timmann, D; Di Fabio, R; Masciullo, M; Baliko, L; Melegh, B; Boesch, S; B?rk, K; Peltz, A; Schulz, Jb; Dufaure Gar?, I; Klockgether, T.
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes. 1.1 Articolo in rivista 1996 Filla, Alessandro; DE MICHELE, Giuseppe; Campanella, G; Perretti, A; Santoro, Lucio; Serlenga, L; Ragno, M; Calabrese, O; Castaldo, I; De Joanna, G; Cocozza, Sergio
Overview of autosomal recessive ataxias. 2.1 Contributo in volume (Capitolo o Saggio) 2012 Filla, Alessandro; DE MICHELE, Giuseppe
Depression comorbidity in spinocerebellar ataxia. 1.1 Articolo in rivista 2011 Schmitz Hübsch, T; Coudert, M; Tezenas du Montcel, S; Giunti, P; Labrum, R; Dürr, A; Ribai, P; Charles, P; Linnemann, C; Schöls, L; Rakowicz, M; Rola, R; Zdzienicka, E; Fancellu, R; Mariotti, C; Baliko, L; Melegh, B; Filla, Alessandro; Salvatore, Elena; van de Warrenburg, Bp; Szymanski, S; Infante, J; Timmann, D; Boesch, S; Depondt, C; Kang, Js; Schulz, Jb; Klopstock, T; Lossnitzer, N; Löwe, B; Frick, C; Rottländer, D; Schlaepfer, Te; Klockgether, T.
Evidence of a genetic marker associated with early onset in Friedreich's ataxia 1.1 Articolo in rivista 1993 Cocozza, Sergio; A., Antonelli; G., Campanella; F., Cavalcanti; DE MICHELE, Giuseppe; S., Di Donato; Filla, Alessandro; A., Monticelli; L., Pianese; A., Piccinelli
A Novel PSEN1 Mutation in a Patient with Sporadic Early-Onset Alzheimer's Disease and Prominent Cerebellar Ataxia. 1.1 Articolo in rivista 2014 Testi, S; Peluso, Silvio; Fabrizi, Gm; Antenora, Antonella; Russo, Cv; Pappat?, S; Padovani, A; Ferrarini, M; Filla, Alessandro