IRIS

DE MICHELE, GIUSEPPE

DE MICHELE, GIUSEPPE  

DIPARTIMENTO DI SCIENZE BIOMEDICHE AVANZATE  

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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
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.
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.
PARK11 is not linked with Parkinson's disease in European families. 1.1 Articolo in rivista 2005 Prestel, J; Sharma, M; Leitner, P; Zimprich, A; Vaughan, Jr; Durr, A; Bonifati, V; DE MICHELE, Giuseppe; Hanagasi, Ha; Farrer, M; Hofer, A; Asmus, F; Volpe, G; Meco, G; Brice, A; Wood, Nw; MULLER MYHSOK, B; Gasser, T.
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.
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
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
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism 1.1 Articolo in rivista 1998 Lücking, Cb; Abbas, N; Dürr, A; Bonifati, V; Bonnet, Am; DE BROUCKER, T; DE MICHELE, Giuseppe; Wood, Nw; Agid, Y; Brice, A.
Genetic mapping of an Italian large pedigree of a new syndrome showing bilateral cataract, gastroesophageal reflux and spastic paraparesis with amyotrophy 1.1 Articolo in rivista 1999 Seri, M; Cusano, R; Forabosco, P; Cinti, R; Caroli, F; Picco, P; Bini, R; BRESCIA MORRA, Vincenzo; DE MICHELE, Giuseppe; Lerone, M; Silengo, M; Pela, I; Borrone, C; Romeo, G; Devoto, M.
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.
Ambulatoy 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, L; Nicolai, E; DE MICHELE, Giuseppe; Campanella, G; Salvatore, M; Postiglione, A. .
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.
Early-onset cerebellar ataxia with retained tendon reflexes 2.1 Contributo in volume (Capitolo o Saggio) 2000 Filla, Alessandro; DE MICHELE, Giuseppe
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-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, Lucio; Davies, S; Hurst, J; Devoto, M; Ravazzolo, R; Seri, M.
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.
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism 1.1 Articolo in rivista 2003 Ibanez, P; DE MICHELE, Giuseppe; Bonifati, V; Lohmann, E; Thobois, S; Pollak, P; Agid, Y; Heutink, P; Durr, A; Brice, A; FRENCH PARKINSON'S DISEASE GENETICS STUDY, Group
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.
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.
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.
How much phenotypic variation can be attributed to parkin genotype? 1.1 Articolo in rivista 2003 Lohmann, E; Periquet, M; Bonifati, V; Wood, Nw; DE MICHELE, Giuseppe; Bonnet, Am; Fraix, V; Broussolle, E; Horstink, Mw; Vidailhet, M; Verpillat, P; Gasser, T; Nicholl, D; Teive, H; Raskin, S; Rascol, O; Destee, A; Ruberg, M; Gasparini, F; Meco, G; Agid, Y; Durr, A; Brice, A; FRENCH PARKINSON'S DISEASE GENETICS STUDY, Group; EUROPEAN CONSORTIUM ON GENETIC SUSCEPTIBILITY IN PARKINSON'S, Disease