DE MICHELE, GIUSEPPE

DE MICHELE, GIUSEPPE  

Dipartimento di Scienze biomediche avanzate  

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A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxia. 1-gen-1993 Filla, Alessandro; DE MICHELE, Giuseppe; Orefice, Giuseppe; F., Santorelli; L., Trombetta; S., Banfi; F., Squitieri; G., Napolitano; D., Puma; G., Campanella
A double-blind, cross-over trial with madopar HBS in patients with Parkinson's disease. 1-gen-1989 DE MICHELE, Giuseppe; A., Mengano; Filla, Alessandro; L., Trombetta; G., Campanella
A genetic study of Parkinson's disease. 1-gen-1995 DE MICHELE, Giuseppe; Filla, Alessandro; R., Marconi; G., Volpe; A., D'Alessio; R., Scala; G., Ambrosio; G., Campanella
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 1-gen-1998 DE MICHELE, Giuseppe; DE FUSCO, M; Cavalcanti, F; Filla, Alessandro; Marconi, R; Volpe, G; Monticelli, A; Ballabio, Andrea; Casari, G; Cocozza, Sergio
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 1-gen-1998 DE MICHELE, Giuseppe; De Fusco, M; Cavalcanti, F; Filla, Alessandro; Marconi, R; Volpe, G; Monticelli, A; Ballabio, Andrea; Casari, G; Cocozza, Sergio
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. . 1-gen-1998 DE MICHELE, Giuseppe; DE FUSCO, M.; Cavalcanti, F.; Filla, Alessandro; Marconi, R.; Volpe, G.; Monticelli, A.; Ballabio, Andrea; Casari, G.; Casari, G.; Cocozza, Sergio
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 1-gen-2007 A. D., Rosa; C., Carducci; I., Antonozzi; T., Giovanniello; E., Xhoxhi; C., Criscuolo; V., Menchise; Striano, Salvatore; Filla, Alessandro; Michele, G. D.
A particular mechanism for the retrieval of the spatial trace in dementia. An Experimental study of 198 subjects. 1-gen-1979 A., Orsini; D., Grossi; DE MICHELE, Giuseppe
A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3. 1-gen-2012 Filla, Alessandro; Sacca', Francesco; DE MICHELE, Giuseppe
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2. 1-gen-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.
A refined physical and transcriptional map of the SPG9 locus on 10q23.3[#150]q24.2 1-gen-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.
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. 1-gen-1999 N., Abbas; C. B., Lücking; S., Ricard; A., Dürr; V., Bonifati; DE MICHELE, Giuseppe; S., Bouley; J. R., Vaughan; T., Gasser; R., Marconi; E., Broussolle; C., Brefel Courbon; B. S., Harhangi; B. A., Oostra; E., Fabrizio; G. A., Böhme; L., Pradier; N. W., Wood; Filla, Alessandro; G., Meco; P., Denefle; Y., Agid; A., Brice
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 1-gen-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
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 1-gen-2000 Filla, Alessandro; DE MICHELE, Giuseppe; Coppola, G; Federico, A; Vita, G; Toscano, A; Uncini, A; Pisanelli, P; Barone, P; Scarano, V; Perretti, A; Santoro, Lucio; Monticelli, A; Cavalcanti, F; Caruso, G; Cocozza, Sergio
Adult normative values for the PATA Rate Test 1-gen-2018 Pane, Chiara; Costabile, Teresa; Salvati, Adriana; Aurisicchio, Dalila Luisa; Abate, Filomena; Liguori, Angese; Paciello, Francesca; Peluso, Silvio; Manganelli, Fiore; De Michele, Giuseppe; Filla, Alessandro; Saccà, Francesco
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy. 1-gen-2001 Barbieri, F; Pellecchia, Mt; Esposito, E; DI STASIO, E; Castaldo, I; Santorelli, F; Perretti, A; Santoro, Lucio; DE MICHELE, Giuseppe
Age of onset, sex, and cardiomyopathy as predictors of disability and survival in Friedreich's disease: a retrospective study on 119 patients. 1-gen-1996 DE MICHELE, Giuseppe; F., Perrone; Filla, Alessandro; E., Mirante; Giordano, Maristella; DE PLACIDO, Sabino; G., Campanella
ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism 1-gen-2015 Panza, Emanuele; Escamilla Honrubia, Juan M; Marco Marín, Clara; Gougeard, Nadine; DE MICHELE, Giuseppe; BRESCIA MORRA, Vincenzo; Liguori, Rocco; Salviati, Leonardo; Donati, Maria Alice; Cusano, Roberto; Pippucci, Tommaso; Ravazzolo, Roberto; Németh, Andrea H; Smithson, Sarah; Davies, Sally; Hurst, Jane A; Bordo, Domenico; Rubio, Vicente; Seri, Marco
Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations 1-gen-2018 Fasano, Dominga; Parisi, Silvia; Pierantoni, Giovanna Maria; De Rosa, Anna; Picillo, Marina; Amodio, Giuseppina; Pellecchia, Maria Teresa; Barone, Paolo; Moltedo, Ornella; Bonifati, Vincenzo; De Michele, Giuseppe; Nitsch, Lucio; Remondelli, Paolo; Criscuolo, Chiara; Paladino, Simona
Alteration of endosomal trafficking is associated with neurodegenerative diseases 1-gen-2018 Fasano, Dominga; Zerillo, Lucrezia; Pierantoni, GIOVANNA MARIA; DE ROSA, Anna; Picillo, Marina; Amodio, Giuseppina; Pellecchia, MARIA TERESA; Barone, Paolo; DE MICHELE, Giuseppe; Sarnataro, Daniela; Nitsch, Lucio; Remondelli, Paolo; Criscuolo, Chiara; Paladino, Simona