IRIS

DE MICHELE, GIUSEPPE

DE MICHELE, GIUSEPPE  

DIPARTIMENTO DI SCIENZE BIOMEDICHE AVANZATE  

Mostra records
Risultati 1 - 20 di 407 (tempo di esecuzione: 0.037 secondi).
Titolo Tipologia Data di pubblicazione Autore(i) File
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.
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.
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.
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.
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
Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy. 1.1 Articolo in rivista 1992 Filla, Alessandro; DE MICHELE, Giuseppe; Marconi, R; Bucci, Luigi; Carillo, C; Castellano, Ae; Iorio, L; Kniahynicki, C; Rossi, F; Campanella, G.
Cerebellar ataxia and hypogonadism. Description of 4 cases. 1.1 Articolo in rivista 1987 DE MICHELE, Giuseppe; Filla, Alessandro; Striano, Salvatore; L., Iorio; B., Merola; M. D., Rosa; G., Lombardi; G., Campanella
Extrapyramidal side-effects of flunarizine. 1.1 Articolo in rivista 1987 DE MICHELE, Giuseppe; Filla, Alessandro; N., Coppola; D., Mansi; B., Morra; G. A., Buscaino
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.
Sexual behaviour in untreated and treated coeliac patients. 1.1 Articolo in rivista 1998 Ciacci, Carolina; A., De Rosa; DE MICHELE, Giuseppe; G., Savino; A., Squillante; Iovino, Paola; F., Sabbatini; G., Mazzacca
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
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
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
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.
Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix-Saguenay 1.1 Articolo in rivista 2008 Garcia, A; Criscuolo, C; DE MICHELE, Giuseppe; Berciano, J.
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.
Etiology of Parkinson's disease. The role of environment and heredity. 1.1 Articolo in rivista 1996 DE MICHELE, Giuseppe; Filla, Alessandro; G., Volpe; A., Gogliettino; G., Ambrosio; G., Campanella
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms. 1.1 Articolo in rivista 2001 N., Vanacore; V., Bonifati; C., Colosimo; G., Fabbrini; DE MICHELE, Giuseppe; R., Marconi; D., Nicholl; N., Locuratolo; S., Romano; G., Talarico; F., Stocchi; U., Bonuccelli; P., Lamberti; P., Vieregge; G., Meco; E. S., Group