IRIS

DE MICHELE, GIUSEPPE

DE MICHELE, GIUSEPPE  

DIPARTIMENTO DI SCIENZE BIOMEDICHE AVANZATE  

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Risultati 1 - 20 di 397 (tempo di esecuzione: 0.032 secondi).
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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.
Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects. 1.1 Articolo in rivista 2009 Vaurs Barrière, C; Deville, M; Sarret, C; Giraud, G; Des Portes, V; Prats Viñas, Jm; DE MICHELE, Giuseppe; Dan, B; Brady, Af; Boespflug Tanguy, O; Touraine, R.
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases. 1.1 Articolo in rivista 2009 Papa, S; Petruzzella, V; Scacco, S; Sardanelli, Am; Iuso, A; Panelli, D; Vitale, R; Trentadue, R; De Rasmo, D; Capitanio, N; Piccoli, Claudia; Papa, F; Scivetti, M; Bertini, E; Rizza, T; DE MICHELE, Giuseppe
Imaging of dopaminergic dysfunction with [123I]FP-CIT SPECT in early-onset parkin disease. 1.1 Articolo in rivista 2004 Varrone, A; Pellecchia, MARIA TERESA; Amboni, Marianna; Sansone, Valeria; Salvatore, Elena; Ghezzi, D; Garavaglia, B; Brice, A; Brunetti, Arturo; Bonavita, Vincenzo; DE MICHELE, Giuseppe; Salvatore, Marco; Pappatà, S; Barone, Paolo
Sex differences in children's spatial and verbal memory span. 1.1 Articolo in rivista 1979 D., Grossi; A., Orsini; C., Monetti; DE MICHELE, Giuseppe
Verbal and spatial memory span in dementia (an experimental study of 185 subjects). 1.1 Articolo in rivista 1978 G., Cantone; A., Orsini; D., Grossi; DE MICHELE, Giuseppe
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case. 1.1 Articolo in rivista 1977 Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele
A refined physical and transcriptional map of the SPG9 locus on 10q23.3[#150]q24.2 1.1 Articolo in rivista 2000 LO NIGRO, C; Cusano, R; Scaranari, M; Cinti, R; Forabosco, P; BRESCIA MORRA, Vincenzo; DE MICHELE, Giuseppe; Santoro, L; Davies, S; Hurst, J; Devoto, M; Ravazzolo, R; Seri, M.
Short-term continuous infusion of apomorphine hydrochloride for treatment of Huntington's chorea: A double blind, randomized cross-over trial 1.1 Articolo in rivista 2007 Vitale, C; Marconi, S; DI MAIO, L; DE MICHELE, Giuseppe; Longo, K; Bonavita, Vincenzo; Barone, Paolo
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. 1.1 Articolo in rivista 2006 Ibanez, P; Lesage, S; Lohmann, E; Thobois, S; DE MICHELE, Giuseppe; Borg, M; Agid, Y; Durr, A; Brice, A; FRENCH PARKINSON'S DISEASE GENETICS STUDY, G. R. O. U. P.
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.
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
Parkin mutations are frequent in patients with isolated early-onset parkinsonism 1.1 Articolo in rivista 2003 Periquet, M; Latouche, M; Lohmann, E; Rawal, N; DE MICHELE, Giuseppe; Ricard, S; Teive, H; Fraix, V; Vidailhet, M; Nicholl, D; Barone, P; Wood, Nw; Raskin, S; Deleuze, Jf; Agid, Y; Durr, A; Brice, A; FRENCH PARKINSON'S DISEASE GENETICS STUDY, Group; EUROPEAN CONSORTIUM ON GENETIC SUSCEPTIBILITY IN PARKINSON'S, Disease
Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23. 1.1 Articolo in rivista 2003 Marconi, R; DE FUSCO, M; Aridon, P; Plewnia, K; Rossi, M; Carapelli, S; Ballabio, Andrea; Morgante, L; Musolino, R; Micieli, G; DE MICHELE, Giuseppe; Casari, G.
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.
Cerebellar ataxia and hypogonadism. A clinicopathological report. 1.1 Articolo in rivista 1990 DE MICHELE, Giuseppe; Filla, Alessandro; D'Armiento, FRANCESCO PAOLO; Striano, Salvatore; Barbieri, F; Salvatore, G; Di Carlo, V; Mansi, D.
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. 1.1 Articolo in rivista 1996 Campuzano, V; Montermini, L; Moltò, Md; Pianese, L; Cossée, M; Cavalcanti, F; Monros, E; Rodius, F; Duclos, F; Monticelli, A; Zara, F; Cañizares, J; Koutnikova, H; Bidichandani, Si; Gellera, C; Brice, A; Trouillas, P; DE MICHELE, Giuseppe; Filla, Alessandro; De Frutos, R; Palau, F; Patel, Pi; Di Donato, S; Mandel, Jl; Cocozza, Sergio; Koenig, M; Pandolfo, M.
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. 1.1 Articolo in rivista 1998 G., Casari; M. D., Fusco; S., Ciarmatori; M., Zeviani; M., Mora; P., Fernandez; DE MICHELE, Giuseppe; Filla, Alessandro; Cocozza, Sergio; R., Marconi; A., Dürr; B., Fontaine; Ballabio, Andrea
Noninvasive assessment of systolic and diastolic function in 50 patients with Friedreich's ataxia. 1.1 Articolo in rivista 1988 Giunta, A; Maione, S; Biagini, R; Filla, Alessandro; DE MICHELE, Giuseppe; Campanella, G.
Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1. 1.1 Articolo in rivista 1998 L., Trojano; Chiacchio, Laura; D., Grossi; A. I., Pisacreta; O., Calabrese; I., Castaldo; DE MICHELE, Giuseppe; Filla, Alessandro