IRIS

FILLA, ALESSANDRO

FILLA, ALESSANDRO  

DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE  

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Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 1.1 Articolo in rivista 2000 Filla, Alessandro; DE MICHELE, Giuseppe; Coppola, G; Federico, A; Vita, G; Toscano, A; Uncini, A; Pisanelli, P; Barone, P; Scarano, V; Perretti, A; Cocozza, Sergio
Early onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q. 1.1 Articolo in rivista 1995 Palau, F; DE MICHELE, Giuseppe; Vilchez, J; Pandolfo, M; Monrs, E; Cocozza, Sergio; Smeyers, P; LOPEZ ARLANDIS, J; Campanella, G; DI DONATO, S; Filla, Alessandro
Cerebellar blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients. 1.1 Articolo in rivista 1998 DE MICHELE, Giuseppe; Mainenti, Pp; Soricelli, A; DI SALLE, F; Salvatore, Elena; Longobardi, Mr; Postiglione, A; Salvatore, M; Filla, Alessandro
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families 1.1 Articolo in rivista 2000 Filla, Alessandro; Mariotti, C; Caruso, G; Coppola, G; Cocozza, Sergio; Castaldo, I; Calabrese, O; Salvatore, Elena; DE MICHELE, Giuseppe; Riggio, Mc; Pareyson, D; Gellera, C; DI DONATO, S.
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. 1.1 Articolo in rivista 2002 Martinez, M; Brice, A; Vaughan, Jr; Zimprich, A; Breteler, Mm; Meco, G; Filla, Alessandro; Farrer, Mj; Betard, C; Singleton, A; Hardy, J; DE MICHELE, Giuseppe; Bonifati, V; Oostra, Ba; Gasser, T; Wood, Nw; Durr, A.
Early-onset cerebellar ataxia with retained tendon reflexes. 1.1 Articolo in rivista 2000 Filla, Alessandro; DE MICHELE, Giuseppe
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family 1.1 Articolo in rivista 2003 DE MICHELE, Giuseppe; Pocchiari, M; Petraroli, R; Manfredi, M; Caneve, G; Coppola, G; Casali, C; Sacca', Francesco; Berardelli, A; Barbieri, Fabrizio; Ghetti, B; Filla, Alessandro
Electrophysiologic characterization in spinocerebellar ataxia 17 1.1 Articolo in rivista 2006 Manganelli, F.; Perretti, ANNA CARMELA AGNESE; Nolano, M.; Lanzillo, B.; Bruni, A. C.; DE MICHELE, Giuseppe; Filla, Alessandro; Santoro, L.
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype 1.1 Articolo in rivista 2005 Criscuolo, C; Mancini, P; Sacca', Francesco; DE MICHELE, Giuseppe; Monticelli, A; Santoro, Lucio; Scarano, V; Banfi, S; Filla, Alessandro
Neurophysiological Evidence of Corticospinal Tract Abnormality in Patients with Parkin Mutations 1.1 Articolo in rivista 2005 DE ROSA, A.; Volpe, G.; Marcantonio, L.; Santoro, L.; Brice, A.; Filla, Alessandro; Perretti, ANNA CARMELA AGNESE; DE MICHELE, Giuseppe
Ataxia with oculomotor apraxia type 1 in southern italy: late onset and variable phenotype. 1.1 Articolo in rivista 2004 Criscuolo, Chiara; Mancini, Pietro; Sacca', Francesco; DE MICHELE, Giuseppe; Monticelli, A; Santoro, Lucio; Scarano, Valentina; Banfi, S; Filla, Alessandro
Serum transferrin receptor levels in Friedreich's and other degenerative ataxias. 1.1 Articolo in rivista 2001 Scarano, V; DE CRISTOFARO, T; DE MICHELE, Giuseppe; Salvatore, Elena; DE BIASE, I; Monticelli, A; Filla, Alessandro; Cocozza, Sergio
Intergenerational instability and marked anticipation in SCA-17. 1.1 Articolo in rivista 2003 Maltecca, F; Filla, Alessandro; Castaldo, I; Coppola, G; Fragassi, Na; Carella, M; Bruni, A; Cocozza, Sergio; Casari, G; Servadio, A; DE MICHELE, Giuseppe
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 1.1 Articolo in rivista 1998 DE MICHELE, Giuseppe; DE FUSCO, M; Cavalcanti, F; Filla, Alessandro; Marconi, R; Volpe, G; Monticelli, A; Ballabio, Andrea; Casari, G; Cocozza, Sergio
SPINOCEREBELLAR ATAXIA 2: A BRAIN DIFFUSION-WEIGHTED MRI STUDY 4.1 Articoli in Atti di convegno 2006 Salvatore, Elena; Mollica, C; Ianniciello, M; Varrone, A; Sansone, V; Salvatore, M; DE MICHELE, Giuseppe; Filla, Alessandro; Pappata, S.
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.
Paroxysmal dystonia in Behcet's disease. 1.1 Articolo in rivista 1999 Pellecchia, Mt; Cuomo, T; Striano, Salvatore; Filla, Alessandro; Barone, P.
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells. 1.1 Articolo in rivista 2002 L., Pianese; L., Busino; I., DE BIASE; T., DE CRISTOFORO; M. S., LO CASALE; P., Giuliano; A., Monticelli; Turano, Mimmo; C., Criscuolo; Filla, Alessandro; S. VARRONE AND S., Cocozza
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease 1.1 Articolo in rivista 1998 Casari, G; DE FUSCO, M; Ciarmatori, S; Zeviani, M; Mora, M; Fernandez, P; DE MICHELE, Giuseppe; Filla, Alessandro; Cocozza, Sergio; Marconi, R; Durr, A; Fontaine, B; Ballabio, Andrea
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, A; Lanzillo, B; Coppola, G; DE JOANNA, G; Manganelli, F; Cocozza, Sergio; DE MICHELE, Giuseppe; Filla, Alessandro; Caruso, G.