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Mostrati risultati da 1 a 19 di 19
Titolo Autore(i) Anno Periodico Editore Tipo File
Videopolygraphic and functional MRI study of musicogenic epilepsy. A case report and literature review. Pittau F.; Tinuper P.; Bisulli F.; Naldi I.; Cortelli P.; Bisulli A.; Stipa C.; Cevolani D.; Agat...i R.; Leonardi M.; Baruzzi A. 2008-01-01 EPILEPSY & BEHAVIOR - 1.01 Articolo in rivista -
Cerebral areas involved in music perception: studying musicogenic epilepsy. Pittau F.; Bisulli F.; Stipa C.; Naldi I.; Licchetta L.; Di Vito L.; Cevolani D.; Agati R.; Tinup...er P. 2010-01-01 - Nova Science Publisher 2.01 Capitolo / saggio in libro -
Neuropsychological impairment in patients with early onset nocturnal frontal lobe epilepsy. Mostacci B.; Bianchi F.; Poda R.; Bisulli F.; Provini F.; Oppi F.; Naldi I.; Licchetta L.; Posar ...A.; Stipa C.; Gallassi R.; Tinuper P. 2011-01-01 EPILEPSIA - 4.02 Riassunto (Abstract) -
Diagnostic accuracy of a structured interview for nocturnal frontal lobe epilepsy (SINFLE): a proposal for developing diagnostic criteria. Bisulli F.; Vignatelli L.; Naldi I.; Pittau F.; Provini F.; Plazzi G.; Stipa C.; Leta C.; Montagn...a P.; Tinuper P. 2012-01-01 SLEEP MEDICINE - 1.01 Articolo in rivista -
Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR) Antelmi E.; Mastrangelo M.; Bisulli F.; Spaccini L.; Stipa C.; Mostacci B.; Mei D.; Guerrini R.; ...Tinuper P. 2012-01-01 EPILEPTIC DISORDERS - 1.01 Articolo in rivista -
Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31. Bisulli F;Naldi I;Baldassari S;Magini P;Licchetta L;Castegnaro G;Fabbri M;Stipa C;Ferrari S;Seri ...M;Gonçalves Silva GE;Tinuper P;Pippucci T 2014-01-01 EPILEPSIA - 1.01 Articolo in rivista -
Pearls & Oy-sters: rapidly progressive dementia: prions or immunomediated? F. Cavallieri;J. Mandrioli;M. Tondelli;F. Vitetta;C. Stipa;S. Vallone;E. Georgoulopoulou;F. Barbi...;R. Liguori;P. Parchi;P. Nichelli 2014-01-01 NEUROLOGY - 1.04 Replica / breve intervento (e simili) -
Auditory aura in nocturnal frontal lobe epilepsy: a red flag to suspect an extra-frontal epileptogenic zone Ferri, Lorenzo; Bisulli, Francesca; Nobili, Lino; Tassi, Laura; Licchetta, Laura; Mostacci, Barba...ra; Stipa, Carlotta; Mainieri, Greta; Bernabè, Giorgia; Provini, Federica; Tinuper, Paolo 2014-01-01 SLEEP MEDICINE - 1.01 Articolo in rivista -
Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions C. La Morgia; L. Caporali; F. Gandini; A. Olivieri; F. Toni; S. Nassetti;
D. Brunetto; C. Stipa;...
C. Scaduto; A. Parmeggiani; C. Tonon; R. Lodi;
A. Torroni; V. Carelli
2014-01-01 BMC NEUROLOGY - 1.01 Articolo in rivista 1471-2377-14-116.pdf
LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF). Magini P;Bisulli F;Baldassari S;Stipa C;Naldi I;Licchetta L;Menghi V;Tinuper P;Seri M;Pippucci T 2014-01-01 EPILEPSY RESEARCH - 1.01 Articolo in rivista -
Epilepsy with auditory features: A heterogeneous clinico-molecular disease Pippucci, T.; Licchetta, L.; Baldassari, S.; Palombo, F.; Menghi, V.; D'Aurizio, R.; Leta, C.; St...ipa, C.; Boero, G.; D'Orsi, G.; Magi, A.; Scheffer, I.; Seri, M.; Tinuper, P.; Bisulli, F. 2015-01-01 NEUROLOGY. GENETICS - 1.01 Articolo in rivista PIPPUCCI_2015_NEUROL GENET_EPILEPSY WITH AUDITORY FEATURES.pdfAdditional Files.zip
Adult patients with intellectual disability and epilepsy: clinical and genetic study of 114 cases Stipa, Carlotta; Licchetta, Laura; Farolfi, A; Paccagnella, E; Magini, P; Pippucci, T; Leta, C; M...enghi, V; Ferri, L; Mostacci, B; Tinuper, Paolo; Bisulli, Francesca 2016-01-01 CLINICAL CASES AND REVIEWS IN EPILEPSY - 1.01 Articolo in rivista -
Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study Vasta, Roberta; Sarica, Alessia; Bisulli, Francesca; Di Gennaro, Giancarlo; D'Aniello, Alfredo; D...ifrancesco, Jacopo C.; Canafoglia, Laura; Casazza, Marina; Franceschetti, Silvana; Stipa, Carlotta; Tinuper, Paolo; Mumoli, Laura; Gambardella, Antonio; Labate, Angelo 2017-01-01 EPILEPSY & BEHAVIOR - 1.01 Articolo in rivista -
Juvenile absence epilepsy relapsing as recurrent absence status, mimicking transient global amnesia, in an elderly patient Muccioli, Lorenzo; Licchetta, Laura; Stipa, Carlotta; Tinuper, Paolo; Bisulli, Francesca 2018-01-01 EPILEPTIC DISORDERS - 1.01 Articolo in rivista -
Effect of valproic acid on perampanel pharmacokinetics in patients with epilepsy. Manuela Contin, Francesca Bisulli,| Margherita Santucci, Roberto Riva,| Francesca Tonon, Susan Mo...hamed, Lorenzo Ferri, Carlotta Stipa, Paolo Tinuper, on behalf of the Perampanel Study Group*, A. Parmeggiani, L. Licchetta 2018-01-01 EPILEPSIA - 1.01 Articolo in rivista -
Epilepsy with auditory features: Long-term outcome and predictors of terminal remission Bisulli, Francesca; Menghi, Veronica; Vignatelli, Luca; Licchetta, Laura; Zenesini, Corrado; Stip...a, Carlotta; Morigi, Francesca; Gizzi, Matteo; Avoni, Patrizia; Provini, Federica; Mostacci, Barbara; d'Orsi, Giuseppe; Pippucci, Tommaso; Muccioli, Lorenzo; Tinuper, Paolo 2018-01-01 EPILEPSIA - 1.01 Articolo in rivista -
Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations Di Vito, Lidia; Licchetta, Laura; Pippucci, Tommaso; Baldassari, Sara; Stipa, Carlotta; Mostacci,... Barbara; Alvisi, Lara; Tinuper, Paolo; Bisulli, Francesca 2018-01-01 EPILEPSY & BEHAVIOR - 1.01 Articolo in rivista -
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late Minardi R.; Licchetta L.; Baroni M.C.; Pippucci T.; Stipa C.; Mostacci B.; Severi G.; Toni F.; Be...rgonzini L.; Carelli V.; Seri M.; Tinuper P.; Bisulli F. 2020-01-01 CLINICAL GENETICS - 1.01 Articolo in rivista Clinical Genetics - 2020 - Minardi - Whole‐exome sequencing in adult patients with developmental and epileptic.pdfcge13823-sup-0003-tables2.docxcge13823-sup-0004-tables3.docxcge13823-sup-0005-supinfo.docx
Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleep Licchetta L.; Di Giorgi L.; Santucci M.; Taruffi L.; Stipa C.; Minardi R.; Carelli V.; Bisulli F. 2024-01-01 MOLECULAR GENETICS & GENOMIC MEDICINE - 1.01 Articolo in rivista Molec Gen Gen Med - 2023 - Licchetta - Biallelic pathogenic variants of PARS2 cause developmental and epileptic.pdf
Mostrati risultati da 1 a 19 di 19
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