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DE MICHELE, GIUSEPPE

DE MICHELE, GIUSEPPE  

DIPARTIMENTO DI SCIENZE BIOMEDICHE AVANZATE  

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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.
POEMS syndrome: clinical, pathological and immunological study of a case 1.1 Articolo in rivista 1994 Orefice, G; BRESCIA MORRA, Vincenzo; DE MICHELE, Giuseppe; Fusco, C; Borgia, G; Cerini, R; Barbieri, F.
Ambulatory monitoring of left ventricular function in patients with Parkinson's disease and postural hypotension 1.1 Articolo in rivista 1994 Nappi, A; Cuocolo, A; Iazzetta, N; Ferrara, LIBERATO ALDO; Marotta, T; Pace, Leonardo; Nicolai, E; DE MICHELE, Giuseppe; Campanella, G; Salvatore, M.
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
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
Association between early-onset Parkinson's disease and parkin gene mutations 1.1 Articolo in rivista 2000 Lücking, Cb; Dürr, A; Bonifati, V; Vaughan, J; DE MICHELE, Giuseppe; Gasser, T; Harhangi, Bs; Meco, G; Denèfle, P; Wood, Nw; Agid, Y; Brice, A.
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy 1.1 Articolo in rivista 2000 Barbieri, F.; Pellecchia, M. T.; Esposito, E.; DI STASIO, E.; Castaldo, I.; Santorelli, F.; Perretti, ANNA CARMELA AGNESE; Santoro, L.; DE MICHELE, Giuseppe
The Sepiapterin Reductase Gene Region Reveals Association in the PARK3 locus: Analysis of Familial and Sporadic Parkinson Disease in European Populations. 1.1 Articolo in rivista 2006 Sharma, M; Mueller, Jc; Zimprich, A; Lichtner, P; Hofer, A; Leitner, P; Maass, S; Berg, D; Durr, A; Bonifati, V; DE MICHELE, Giuseppe; Oostra, B; Brice, A; Wood, Nw; Myhsok, Bm; Gasser, T.
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
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.
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.