IRIS

SANTORO, LUCIO

SANTORO, LUCIO  

DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE  

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Risultati 1 - 20 di 326 (tempo di esecuzione: 0.05 secondi).
Titolo Tipologia Data di pubblicazione Autore(i) File
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score. 1.1 Articolo in rivista 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, G; Galluzzi, G; Rodolico, C; Santoro, Lucio; Tomelleri, G; Angelini, C; Ricci, E; Palmucci, L; Moggio, M; Tupler, R.
Case of Myhre syndrome with autism and peculiar skin histological findings 1.1 Articolo in rivista 2001 Titomanlio, L; Marzano, Mg; Rossi, E; D'Armiento, M; De Brasi, D; Vega, Gr; Andreucci, Mv; Orsini, Av; Santoro, Lucio; Sebastio, Gianfranco
Electrophysiological and histological follow-up study in 15 Friedreich's ataxia patients 1.1 Articolo in rivista 1990 Santoro, Lucio; Perretti, A.; Crisci, C.; Ragno, M.; Massini, R.; Filla, A.; DE MICHELE, G.; Caruso, G.
Adult-onset Alexander disease : Report on a family. 1.1 Articolo in rivista 2008 Balbi, P; Seri, M; Ceccherini, I; Uggetti, C; Casale, R; Fundar, C; Caroli, F; Santoro, Lucio
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria 1.1 Articolo in rivista 2001 Spelbrink, Jn; Li, Fy; Tiranti, V; Nikali, K; Yuan, Qp; Tariq, M; Wanrooij, S; Garrido, N; Comi, G; Morandi, L; Santoro, Lucio; Toscano, A; Fabrizi, Gm; Somer, H; Croxen, R; Beeson, D; Poulton, J; Suomalainen, A; Jacobs, Ht; Zeviani, M; Larsson, C.
Internodal length variability of dermal myelinated fibres. 1.1 Articolo in rivista 2010 Nolano, M; Provitera, V; Santoro, Lucio
ERRATUM: Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria. 1.7 Commento, erratum, replica e simili 2001 Spelbrink, Jn; Li, Fy; Tiranti, V; Nikali, K; Yuan, Qp; Tariq, M; Wanrooij, S; Garrido, N; Comi, G; Morandi, L; Santoro, Lucio; Toscano, A; Fabrizi, Gm; Somer, H; Croxen, R; Beeson, D; Poulton, J; Suomalainen, A; Jacobs, Ht; Zeviani, M; Larsson, C.
Small-fiber involvement in spinobulbar muscular atrophy (Kennedy's disease). 1.1 Articolo in rivista 2007 Manganelli, Fiore; Iodice, V; Provitera, V; Pisciotta, C; Nolano, M; Perretti, A; Santoro, Lucio
Neurophysiologic evaluation of central-peripheral sensory and motor pudendal pathways in primary premature ejaculation. 1.1 Articolo in rivista 2003 Perretti, A; Catalano, A; Mirone, Vincenzo; Imbimbo, C; Balbi, P; Palmieri, A; Longo, N; Fusco, Ferdinando; Verze, P; Santoro, Lucio
Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease 1.1 Articolo in rivista 2002 Bruno, C; Lanzillo, Roberta; Biedi, C; Iadicicco, L; Minetti, C; Santoro, Lucio
Case of acute motor conduction block neuropathy (AMCBN) 1.1 Articolo in rivista 2009 Manganelli, Fiore; Pisciotta, C; Iodice, Rosa; Calandro, S; Dubbioso, R; Ranieri, A; Santoro, Lucio; Dubbioso, Raffaele
Validation of the Italian version of the Neuropathic Pain Symptom Inventory in peripheral nervous system diseases 1.1 Articolo in rivista 2009 Padua, L; Briani, C; Jann, S; Nobile Orazio, E; Pazzaglia, C; Morini, A; Mondelli, M; Ciaramitaro, P; Cavaletti, G; Cocito, D; Fazio, R; Santoro, Lucio; Galeotti, F; Carpo, M; Plasmati, R; Benedetti, L; Schenone, A; Marchettini, P; Cruccu, G.
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency 1.1 Articolo in rivista 2000 Santoro, Lucio; Carrozzo, R; Malandrini, A; Piemonte, F; Patrono, C; Villanova, M; Tessa, A; Palmeri, S; Bertini, E; Santorelli, F. M.
Brain MRI features of congenital- and adult-form myotonic dystrophy type 1: case-control study 1.1 Articolo in rivista 2002 Di Costanzo, A; Di Salle, F; Santoro, Lucio; Bonavita, V; Tedeschi, G.
Pattern and significance of white matter abnormalities in myotonic dystrophy type 1: an MRI study. 1.1 Articolo in rivista 2002 Di Costanzo, A; Di Salle, F; Santoro, Lucio; Tessitore, A; Bonavita, V; Tedeschi, G.
Dilated Virchow-Robin spaces in myotonic dystrophy: frequency, extent and significance 1.1 Articolo in rivista 2001 Di Costanzo, A; Di Salle, F; Santoro, Lucio; Bonavita, V; Tedeschi, G.
Patterns of motor control reorganization in a patient with mirror movements 1.1 Articolo in rivista 2000 Balbi, P; Trojano, L; Ragno, M; Perretti, A; Santoro, Lucio
Late recovery after traumatic, anoxic, or hemorrhagic long-lasting vegetative state. 1.1 Articolo in rivista 2010 Estraneo, A; Moretta, P; Loreto, V; Lanzillo, B; Santoro, Lucio; Trojano, L.
Evolution of gastric electrical features and gastric emptying in children with duchenne and becker muscular dystrophy. 1.1 Articolo in rivista 2005 Borrelli, O; Salvia, G; Mancini, V; Santoro, Lucio; Tagliente, F; Romeo, Ef; Cucchiara, S.
Postexercise facilitation of motor evoked potentials following transcranial magnetic stimulation. A study in normal subjects 1.1 Articolo in rivista 2002 Balbi, P.; Perretti, ANNA CARMELA AGNESE; Sannino, M.; Marcantonio, L.; Santoro, Lucio