SICILIANO, GABRIELE Statistiche

SICILIANO, GABRIELE  

DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE  

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A 5-year clinical follow-up study from the Italian National Registry for FSHD 1-gen-2020 Vercelli, L.; Mele, F.; Ruggiero, L.; Sera, F.; Tripodi, S.; Ricci, G.; Vallarola, A.; Villa, L.; Govi, M.; Maranda, L.; Di Muzio, A.; Scarlato, M.; Bucci, E.; Maggi, L.; Rodolico, C.; Moggio, M.; Filosto, M.; Antonini, G.; Previtali, S.; Angelini, C.; Berardinelli, A.; Pegoraro, E.; Siciliano, G.; Tomelleri, G.; Santoro, L.; Mongini, T.; Tupler, R.
A case of pelvic floor myoclonic jerk syndrome. 1-gen-1996 Ceravolo, Roberto; Nuti, A; Siciliano, Gabriele; Calabrese, R; Bonuccelli, Ubaldo; Cellai, F.
A computer-assisted study of silent period in patients with ALS 1-gen-1999 Siciliano, Gabriele; Manca, MARIA LAURA; Sagliocco, L; Pastorini, E; Pellegrinetti, A; Sartucci, Ferdinando; Sabatini, A; Murri, L.
A mitochondrial tRNAPhe mutation causes MERRF syndrome [Sindrome MERRF associata a mutazione del tRNAPhe] 1-gen-2005 Pizzanelli, C; Galli, Renato; Mancuso, Michelangelo; Virgili, Mp; Geri, G; Chiari, A; Jensen, S; Iudice, Alfonso; Siciliano, Gabriele; Murri, Luigi
A new truncating MPZ mutation associated with a very mild CMT1 B phenotype 1-gen-2010 Piazza, S; Baldinotti, F; Fogli, A; Conidi, Me; Michelucci, A; CALDARAZZO IENCO, Elena; Mancuso, Michelangelo; Simi, P; Siciliano, Gabriele
A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation 1-gen-2004 Mancuso, Michelangelo; Filosto, M; Forli, Francesca; Rocchi, A; Berrettini, Stefano; Siciliano, Gabriele; Murri, Luigi
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia. 1-gen-2011 Souilem, S; Chebel, S; Mancuso, Michelangelo; Petrozzi, Lucia; Siciliano, Gabriele; Frihayed, M; Hentati, F; Amouri, R.
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome 1-gen-2004 Mancuso, Michelangelo; Filosto, M; Mootha, Vk; Rocchi, A; Pistolesi, S; Murri, Luigi; Dimauro, S; Siciliano, Gabriele
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E 1-gen-2005 Andrigo, C; Boito, C; Prandini, P; Mostacciuolo, Ml; Siciliano, Gabriele; Angelini, C; Pegoraro, E.
A personal monitoring architecture to detect muscular fatigue in elderly. 1-gen-2012 Tartarisco, Gennaro; Billeci, L; Ricci, G; Volpi, L; Pioggia, Giovanni; Siciliano, Gabriele
A screening for superoxide dismutase-1 d90a mutation in italian patients with sporadic amyotrophic lateral sclerosis 1-gen-2002 Mancuso, Michelangelo; Filosto, M; Naini, A; Rocchi, A; DEL CORONA, A; Sartucci, Ferdinando; Siciliano, Gabriele; Murri, L.
A SER326CYS POLYMORPHISM IN THE DNA REPAIR GENE HOGG1 IS NOT ASSOCIATED WITH SPORADIC ALZHEIMER'S DISEASE 1-gen-2007 Coppede', Fabio; Mancuso, Michelangelo; LO GERFO, A; Manca, MARIA LAURA; Petrozzi, L; Migliore, Lucia; Siciliano, Gabriele; Murri, Luigi
A STANDARDIZED CLINICAL EVALUATION OF PATIENTS AFFECTED BY FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY: THE FSHD CLINICAL SCORE 1-gen-2010 Lamperti, C; Fabbri, G; Vercelli, L; D'Amico, R; Frusciante, R; Bonifazi, E; Fiorillo, C; Borsato, C; Cao, M; Servida, M; Greco, F; Di Leo, R; Volpi, L; Manzoli, C; Cudia, P; Pastorello, E; Ricciardi, L; Siciliano, Gabriele; Galluzzi, G; Rodolico, C; Santoro, L; Tomelleri, G; Angelini, Carlo; Ricci, E; Palmucci, L; Moggio, M; Tupler, R.
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis 1-gen-2009 Chiò, A; Schymick, Jc; Restagno, G; Scholz, Sw; Lombardo, F; Lai, Sl; Mora, G; Fung, Hc; Britton, A; Arepalli, S; Gibbs, Jr; Nalls, M; Berger, S; Kwee, Lc; Oddone, Ez; Ding, J; Crews, C; Rafferty, I; Washecka, N; Hernandez, D; Ferrucci, L; Bandinelli, S; Guralnik, J; Macciardi, F; Torri, F; Lupoli, S; Chanock, Sj; Thomas, G; Hunter, Dj; Gieger, C; Wichmann, He; Calvo, A; Mutani, R; Battistini, S; Giannini, F; Caponnetto, C; Mancardi, Gl; LA BELLA, V; Valentino, F; Monsurrò, Mr; Tedeschi, G; Marinou, K; Sabatelli, M; Conte, A; Mandrioli, J; Sola, P; Salvi, F; Bartolomei, I; Siciliano, Gabriele; Carlesi, Cecilia; Orrell, Rw; Talbot, K; Simmons, Z; Connor, J; Pioro, Ep; Dunkley, T; Stephan, Da; Kasperaviciute, D; Fisher, Em; Jabonka, S; Sendtner, M; Beck, M; Bruijn, L; Rothstein, J; Schmidt, S; Singleton, A; Hardy, J; Traynor, Bj
A wearable pervasive platform for intelligent monitoring of muscular fatigue 1-gen-2010 Pioggia, G.; Tartarisco, G.; Ricci, G.; Siciliano, Gabriele; DE ROSSI, DANILO EMILIO; Bonfiglio, S.
Abnormal H-Tfam in a patient harboring a single mtDNA deletion. 1-gen-2000 Tessa, A; Manca, MARIA LAURA; Mancuso, Michelangelo; Renna, Mr; Murri, Luigi; Martini, B; Santorelli, Fm; Siciliano, Gabriele
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies. 1-gen-2000 Siciliano, Gabriele; Mancuso, Michelangelo; Pasquali, Livia; Manca, MARIA LAURA; Tessa, A; Iudice, Alfonso
[Abrupt shift to zolpidem, a new imidazopyridine hypnotic, in insomniac patients previously treated with benzodiazepine hypnotics]. 1-gen-1993 Ciapparelli, A; Colombo, C; Cuccato, G; Levi Minzi, A; Lorizio, A; Maggioni, M; Siciliano, Gabriele; Silvestri, R; Biondi, F; Casadei, Gl
Absence of angiogenic genes modification in Italian ALS patients 1-gen-2008 DEL BO, R; Scarlato, M; Ghezzi, S; MARTINELLI BONESCHI, F; Corti, S; Locatelli, F; Santoro, D; Prelle, A; Briani, C; Nardini, M; Siciliano, Gabriele; Mancuso, Michelangelo; Murri, Luigi; Bresolin, N; Comi, Gp
Activity of protein phosphotase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosis patients 1-gen-2004 Ferri, A; Nencini, M; Battistini, S; Giannini, F; Siciliano, Gabriele; Casali, C; Damiano, Mg; Ceroni, M; Chio, A; Rotilio, G; Carri, Mt