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STRIANO, SALVATORE

STRIANO, SALVATORE  

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Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsy. 1.1 Articolo in rivista 2005 Striano, P; Madia, F; Minetti, C; Striano, Salvatore; Zara, F.
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 1.1 Articolo in rivista 2004 Striano, P; Chifari, R; Striano, Salvatore; DE FUSCO, M; Elia, M; Guerrini, R; Casari, G; Canevini, Mp
A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism. 1.1 Articolo in rivista 2005 Striano, P; Elia, M; Castiglia, L; Galesi, O; Pelligra, S; Striano, Salvatore
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 1.1 Articolo in rivista 2007 Striano, P; Zara, F; Coppola, A; Ciampa, C; Pezzella, M; Striano, Salvatore; Coppola, Antonietta
Epileptic seizures can follow high doses of oral vardenafil. 1.1 Articolo in rivista 2006 Striano, P; Zara, F; Minetti, C; Striano, Salvatore
Antiepileptic Drugs and MTHFR Polymorphisms Influence Hyper-Homocysteinemia Recurrence in Epileptic Patients. 1.1 Articolo in rivista 2007 Belcastro, V; Gaetano, G; Italiano, D; Oteri, G; Caccamo, D; Pisani, Lr; Striano, P; Striano, Salvatore; Ientile, R; Pisani, F.
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus. One autopsy case. 1.1 Articolo in rivista 2006 Striano, P; Pagliuca, M; Andreone, V; Zara, F; Coppola, A; Striano, Salvatore; Coppola, Antonietta
IDIOPATHIC PARTIAL EPILEPSY WITH AUDITORY FEATURES (IPEAF): A CLINICAL AND GENETIC STUDY OF 53 SPORADIC CASES 1.1 Articolo in rivista 2004 Bisulli, F; Tinuper, P; Avoni, P; Striano, P; Striano, Salvatore; D'Orsi, G; Vignatelli, L; Bagattin, A; Scudellaro, E; Florindo, I; Nobile, C; Tassinari, Ca; Baruzzi, A; Michelucci, R.
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases 1.1 Articolo in rivista 2006 Striano, P; Malacarne, M; Cavani, S; Pierluigi, M; Rinaldi, R; Cavaliere, Ml; Rinaldi, Mm; DE BERNARDO, C; Coppola, A; Pintaudi, M; Gaggero, R; Grammatico, P; Striano, Salvatore; Dallapiccola, B; Zara, F; Faravelli, F.
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations 1.1 Articolo in rivista 2007 Striano, P; Mancardi, Mm; Biancheri, R; Madia, F; Gennaro, E; Paravidino, R; Beccaria, F; Capovilla, G; DALLA BERNARDINA, B; Darra, F; Elia, M; Giordano, L; Gobbi, G; Granata, T; Ragona, F; Guerrini, R; Marini, C; Mei, D; Longaretti, F; Romeo, A; Siri, L; Specchio, N; Vigevano, F; Striano, Salvatore; Tortora, F; Rossi, A; Minetti, C; Dravet, C; Gaggero, R; Zara, F.
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. 1.1 Articolo in rivista 2006 AYERDI IZQUIERDO, A; Stavrides, G; SELLES MARTINEZ, Jj; Larrea, L; Bovo, G; LOPEZ DE MUNAIN, A; Bisulli, F; MARTI MASSO, Jf; Michelucci, R; Poza, Jj; Tinuper, P; Stephani, U; Striano, P; Striano, Salvatore; Staub, E; Sarafidou, T; Hinzmann, B; Moschonas, N; Siebert, R; Deloukas, P; Nobile, C; PEREZ TUR, J.
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 1.1 Articolo in rivista 2007 Striano, P; Coppola, A; Pezzella, M; Ciampa, C; Specchio, N; Ragona, F; Mancardi, Mm; Gennaro, E; Beccaria, F; Capovilla, G; Rasmini, P; Besana, D; Coppola, Gg; Elia, M; Granata, T; Vecchi, M; Vigevano, F; Viri, M; Gaggero, R; Striano, Salvatore; Zara, F.; Coppola, Antonietta
Inherited neuromyotonia: A clinical and genetic study of a family. 1.1 Articolo in rivista 2007 Falace, A; Striano, P; Manganelli, Fiore; Coppola, A; Striano, Salvatore; Minetti, C; Zara, F.; Coppola, Antonietta
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study. 1.1 Articolo in rivista 2006 Striano, P; Coppola, A; Vacca, G; Zara, F; BRESCIA MORRA, Vincenzo; Orefice, Giuseppe; Striano, Salvatore; Coppola, Antonietta
Clinical and genetic findings in 26 Italian patients with Lafora disease. 1.1 Articolo in rivista 2006 Franceschetti, S; Gambardella, A; Canafoglia, L; Striano, P; Lohi, H; Gennaro, E; Ianzano, L; Veggiotti, P; Sofia, V; Biondi, R; Striano, Salvatore; Gellera, C; Annesi, G; Madia, F; Civitelli, D; Rocca, Fe; Quattrone, A; Avanzini, G; Minassian, B; Zara, F.
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 1.1 Articolo in rivista 2007 Striano, P; Specchio, N; Biancheri, R; Cannelli, N; Simonati, A; Cassandrini, D; Rossi, A; Bruno, C; Fusco, L; Gaggero, R; Vigevano, F; Bertini, E; Zara, F; Santorelli, Fm; Striano, Salvatore
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy. 1.1 Articolo in rivista 2007 Annesi, F; Gambardella, A; Michelucci, R; Bianchi, A; Marini, C; Canevini, Mp; Capovilla, G; Elia, M; Buti, D; Chifari, R; Striano, P; Rocca, Fe; Castellotti, B; Cali, F; Labate, A; Lepiane, E; Besana, D; Sofia, V; Tabiadon, G; Tortorella, G; Vigliano, P; Vignoli, A; Beccaria, F; Annesi, G; Striano, Salvatore; Aguglia, U; Guerrini, R; Quattrone, A.
Relationship between serum mono-hydroxy-carbazepine concentrations and adverse effects in patients with epilepsy on high-dose oxcarbazepine therapy. 1.1 Articolo in rivista 2006 Striano, Salvatore; Striano, P; DI NOCERA, P; Italiano, D; Fasiello, C; Ruosi, P; Bilo, Leonilda; Pisani, F.
Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. 1.1 Articolo in rivista 2005 Striano, P; Zara, F; Striano, Salvatore
Cutis verticis gyrata--mental deficiency syndrome: a patient with drug-resistant epilepsy and polymicrogyria. 1.1 Articolo in rivista 1996 Striano, Salvatore; Ruosi, P; Guzzetta, V; Perone, L; Manto, A; Cirillo, S.