DE MICHELE, GIUSEPPE

DE MICHELE, GIUSEPPE  

DIPARTIMENTO DI SCIENZE BIOMEDICHE AVANZATE  

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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
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.
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
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.
Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia. 1.1 Articolo in rivista 2010 Pagani, E; Ginestroni, A; Della Nave, R; Agosta, F; Salvi, F; DE MICHELE, Giuseppe; Piacentini, S; Filippi, M; Mascalchi, 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
Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease. 1.1 Articolo in rivista 2009 Aziz, Na; Jurgens, Ck; Landwehrmeyer, Gb; EHDN Registry Study, Group; van Roon Mom, Wm; van Ommen, Gj; Stijnen, T; Bachoud Levi AC, Roos R. A.; Bentivoglio, Ar; Biunno, I; Bonelli, R; Burgunder, Jm; Dunnett, Sb; Ferreira, J; Handley, Oj; Heiberg, A; Illmann, T; Landwehrmeyer, Gb; Levey, J; Nielsen, Je; Päivärinta, M; Roos, Ra; Rojo Sebastian, A; Tabrizi, Sj; Vandenberghe, W; Verellen Dumoulin, C; Zaremba, J; Uhrova, T; Wahlstrom, J; Schwenke, C; Orth, M; Illmann, T; Wallner, M; Barth, K; Bascunana Garde, M; Ros, R; Ecker, D; Handley, Oj; Heinonen, N; Held, C; Laura, M; Martinez Descals, A; Mestre, T; Monza, D; Naji, J; Orth, M; Padieu, H; Pro Koivisto, S; Rialland, A; Sasinkova, P; Trigo Cubillo, P; van Walsem, M; Witjes Ane, Mn; Zielonka, D; Bonelli, Rm; Herranhof, B; Hodl, A; Koppitz, M; Magnet, M; Otti, D; Painold, A; Reisinger, K; Flamez, A; Morez, V; de Raedt, S; Ribai, P; Verellen Dumoulin, C; Vandenberghe, W; Van Reijen, D; Hasholt, L; Hjermind, Le; Jakobsen, O; Norremolle, A; Sorensen, Sa; Stokholm, J; Peippo, M; Sipponen, M; Hiivola, H; Martikainen, K; Tuuha, K; Kosinski, Cm; Probst, D; Sass, C; Schiefer, J; Schlangen, C; Werner, Cj; Priller, J; Prüb, H; Andrich, J; Hoffmann, R; Kraus, P; Prehn, C; Saft, C; Salmen, S; Strabburger, K; Lange, H; Hunger, U; Löhle, M; Schmidt, S; Storch, A; Wolz, A; Wolz, M; Lammbeck, J; Zucker, B; Hidding, U; Münchau, A; Orth, M; Stubbe, L; Heinicke, W; Longinus, B; Möller, Jc; Rissling, I; Peinemann, A; Städtler, M; Weindl, A; Bohlen, S; Reilmann, R; Beuster, A; Dose, M; Leythaeuser, G; Marquard, R; Schrenk, C; Schuierer, M; Wiedemann, A; Ecker, D; Landwehrmeyer, B; Lezius, F; Trautmann, S; Bertini, E; Mechi, C; Paganini, M; Piacentini, S; Romoli, M; Sorbi, S; Abbruzzese, G; Bandettini di Poggio, M; Ferrandes, G; Mandes, P; Marchese, R; Albanese, A; Di Donato, S; Mariotti, C; Soliveri, P; Carlo, R; Luigi, Dm; DE MICHELE, Giuseppe; Rinaldi, Carlo; Salvatore, Elena; Tucci, Tecla; Ciarmielo, A; Martino, T; Simonelli, M; Squitieri, F; Bentivoglio, Ar; Fasano, A; Frontali, M; Guidubaldi, A; Lalongo, T; Jacopini, G; Loria, G; Piano, C; Romano, S; Soleti, F; Spadaro, M; Zinzi, P; Heiberg, A; van Walsem, Mr; Bjørgo, K; Fannemel, M; Gørvell, P; Retterstøl, L; Bjørnevoll, I; Sando, Sb; Sitek, Ej; Slawek, J; Soltan, W; Rudzinska, M; Szczudlik, A; Wójcik, M; Bryl, A; Ciesielska, A; Klimberg, A; Kozubski, W; Marcinkowski, J; Sempolowicz, Pj; Zielona, D; Janik, P; Kalbarczyk, A; Kwiecinski, H; Jamrozik, Z; Antczak, J; Rakowicz, M; Richter, P; Ryglewicz, D; Zaremba, J; Zdzienicka, E; Costa, C; Coelho, M; Ferreira, Jj; Mestre, T; Rosa, Mm; Valadas, A; Gago, M; Garrett, C; Guerra, Mr; Bas, J; Calopa, M; Barberà, Ma; Badenes, D; Casas, L; Arroyo, Se; Vara, Jh; Krupinski, J; López, J; Obdulia, M; Ferrer, Pq; Sebastián, Ar; Contreras, Sr; Carruesco, Gt; Cubo, E; Mariscal, N; Sánchez, J; Barrero, Fj; Morales, B; Garcia Ramos Garcia, R; Pin Quiroga, P; Villanueva, C; Ruiz Espiga, Pj; Martinez, A; Saiz Artiga, Mj; Sánchez, V; Bascuñana, M; Fatas, M; Ribas, Gg; de Yébenes, Jg; López Moreno, Jl; Schwarz, C; Cubillo, Pt; Arques, Pn; Gorospe, A; Legarda, I; Rodriguez, Mj; Gaston, I; Ramos Arroyo, Ma; del Val, Jl; Martinez, L; Burgunder, Jm; Romero, I; Schüpbach, M; Zaugg, Sw; van Hout, Ms; van Vugt, Jp; de Weert, Am; Bolwijn, Jj; Dekker, M; Leenders, Kl; van Oostrom, Jc; Bos, R; Dumas, E; Jurgens, Ck; Roos, Ra; Witjes Ané, Mn; Matheson, K; Rae, D; Simpson, S; Summers, F; Ure, A; Curtis, A; Keylock, J; Rickards, H; Wright, J; Barker, Ra; Fisher, K; Goyder Goodman, Ao; Hill, S; Kershaw, A; Mason, S; Paterson, N; Raymond, L; Bisson, J; Busse, M; Ellison Rose, L; Handley, O; Naji, J; Price, K; Rosser, A; Edwards, M; De Sousa, Pa; Hughes, T; Mcgill, M; Pearson, P; Porteous, M; Zema, A; Brockie, P; Foster, J; Johns, N; Mckenzie, S; Thomas, G; Burrows, L; Fletcher, A; Laver, F; Silva, M; Thomas, A; Chu, C; Hobson, E; Jamieson, S; Toscano, J; Wild, S; Yardumian, P; Bourne, C; Clayton, C; Dipple, H; Grant, J; Gross, D; Hallam, C; Middleton, J; Murch, A; Andrews, T; Dougherty, A; Kavalier, F; Golding, C; Lashwood, A; Robertson, D; Ruddy, D; Whaite, A; Andrews, T; Bruno, S; Golding, C; Henley, S; O'Driscoll, C; Patel, A; Rosser, E; Tabrizi, S; Taylor, R; Warner, T; Wild, E; Arran, N; Craufurd, D; Fullam, R; Howard, L; Huson, S; Partington Jones, L; Ritchie, N; Snowden, J; Solom, A; Stopford, C; Thompson, J; Westmoreland, L; Nemeth, Ah; Siuda, G; Bandmann, O; Bradbury, A; Fillingham, K; Foustanos, I; Quarrell, O; Reynders, H; Robertson, L; Tidswell, K.
insulin-like growth factor-1 predicts cognitive functions at 2-year follow-up in early,drug-naive Parkinson's disease. 1.1 Articolo in rivista 2013 Pellecchia, Mt; Santangelo, G; Piccillo, M; Pivonello, Rosario; Longo, K; Pivonello, C; Vitale, C; Amboni, M; De Rosa, Anna; Moccia, M; Erro, R; De Michele, Giuseppe; Santoro, L; Colao, A; Barone, P.
Alternating Hemiplegia of childhood: a family with possibile recessive inherithance 1.5 Abstract in rivista 2004 A., De Falco; V., Scarano; M., Buongiorno; Bilo, Leonilda; E., Marano; DE MICHELE, Giuseppe; Filla, Alessandro
Intergenerational instability and marked anticipation in SCA-17. 1.1 Articolo in rivista 2003 Maltecca, F; Filla, Alessandro; Castaldo, I; Coppola, G; Fragassi, Na; Carella, M; Bruni, A; Cocozza, Sergio; Casari, G; Servadio, A; DE MICHELE, Giuseppe