Sfoglia per Autore
Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31.
2014 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
LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF).
2014 Magini P;Bisulli F;Baldassari S;Stipa C;Naldi I;Licchetta L;Menghi V;Tinuper P;Seri M;Pippucci T
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations
2014 Scheffer, Ingrid E; Heron, Sarah E; Regan, Brigid M; Mandelstam, Simone; Crompton, Douglas E; Hodgson, Bree L; Licchetta, Laura; Provini, Federica; Bisulli, Francesca; Vadlamudi, Lata; Gecz, Jozef; Connelly, Alan; Tinuper, Paolo; Ricos, Michael G; Berkovic, Samuel F; Dibbens, Leanne M
Limbic encephalitis with anti-GAD antibodies and Thomsen myotonia: A casual or causal association?
2014 Licchetta, L.; Bisulli, F.; Naldi, I.; Mainieri, G.; Tinuper, P.
Progressive myoclonic epilepsies: definitive and still undetermined causes
2014 Franceschetti S.; Michelucci R.; Canafoglia L.; Striano P.; Gambardella A.; Magaudda A.; Tinuper P.; La Neve A.; Ferlazzo E.; Gobbi G.; Giallonardo A.T.; Capovilla G.; Visani E.; Panzica F.; Avanzini G.; Tassinari C.A.; Bianchi A.; Zara F.; Bisulli F.; Posar A.; Santucci M.; Licchetta L.; (Collaborative LICE study group on PMEs)
Tailored surgery for drug-resistant epilepsy due to temporal pole encephalocele and microdysgenesis.
2014 M. Giulioni;L. Licchetta;F. Bisulli;G. Rubboli;B. Mostacci;G. Marucci;M. Martinoni;L. Ferri;L. Volpi;F. Calbucci;A. Baruzzi;P. Tinuper
Response to the letter "New avenues to prevent sudden unexpected death in nocturnal frontal lobe epilepsy: follow the route established by omega-3 polyunsaturated fatty acids".
2015 B. Mostacci;F. Bisulli;L. Vignatelli;L. Licchetta;L. D. Vito;C. Rinaldi;I. Trippi;L. Ferri;G. Plazzi;F. Provini;P. Tinuper
A prospective study of direct medical costs in a large cohort of consecutively enrolled patients with refractory epilepsy in Italy
2015 Chiara Luoni; Maria Paola Canevini; Giuseppe Capovilla; Giovambattista De Sarro; Carlo Andrea Galimberti; Giuliana Gatti; Renzo Guerrini; Angela La Neve; Iolanda Mazzucchelli; Eleonora Rosati; Luigi Maria Specchio; Salvatore Striano; Paolo Tinuper; Emilio Perucca; Study of Outcome of PHarmacoresistance In Epilepsy (SOPHIE) collaborators; Agostino Baruzzi; Erminio Bonizzoni; Cinzia Fattore; Valentina Franco; Ambra Malerba; Mario Marzanatti; Veriano Alexandre Jr; Francesca Beccaria; Francesca Bisulli; Sophie Cagdas; Clotilde Ciampa; Luigi Del Gaudio; Benedetta Frassine; Antonio Gambardella; Simone Gana; Lucio Giordano; Angelo Labate; Francesca La Briola; Marianna Ladogana; Laura Licchetta; Giancarlo Muscas; Anna Maria Papantonio; Angelo Pascarella; Simona Pellacani; Lia Santulli; Pasquale Striano; Salvatore Striano; Alessandra Tiberti; Rossana Tozzi; Marina Trivisano
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
2015 Hildebrand M.S.; Tankard R.; Gazina E.V.; Damiano J.A.; Lawrence K.M.;Dahl H-H. M.; Regan B.M.; Shearer A.E.; Smith R.J.H.; Marini C.; Guerrini R.; Labate A.; Gambardella A.; Tinuper P.; Licchetta L.; Baldassari S.; Bisulli F.; Pippucci T.; Scheffer I.E.; Reid C.A.; Petrou S.; Bahlo M.; Berkovic S.F.
Incidence of sudden unexpected death in nocturnal frontal lobe epilepsy: a cohort study.
2015 B. Mostacci;F. Bisulli;L. Vignatelli;L. Licchetta;L. D. Vito;C. Rinaldi;I. Trippi;L. Ferri;G. Plazzi;F. Provini;P. Tinuper
Prevalence of Nocturnal Frontal Lobe Epilepsy in the Adult Population of Bologna and Modena, Emilia-Romagna Region, Italy.
2015 L. Vignatelli;F. Bisulli;G. Giovannini;L. Licchetta;I. Naldi;B. Mostacci;G. Rubboli;F. Provini;P. Tinuper;S. Meletti
A Novel Mutation af Cln3 Associated with Delayed-Classic Juvenile Ceroid Lipofucinois and Autophagic Vacuolar Myopathy
2015 Licchetta, L; Bisulli, F; Fietz, M; Valentino, M L; Morbin, M; Mostacci, B; Oliver, K L; Berkovic, S F; Tinuper, P
Epilepsy with auditory features: A heterogeneous clinico-molecular disease
2015 Pippucci, T.; Licchetta, L.; Baldassari, S.; Palombo, F.; Menghi, V.; D'Aurizio, R.; Leta, C.; Stipa, C.; Boero, G.; D'Orsi, G.; Magi, A.; Scheffer, I.; Seri, M.; Tinuper, P.; Bisulli, F.
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
2015 Muona, M.; Berkovic, S.F.; Dibbens, L.M.; Oliver, K.L.; Maljevic, S.; Bayly, M.A.; Joensuu, T.; Canafoglia, L.; Franceschetti, S.; Michelucci, R.; Markkinen, S.; Heron, S.E.; Hildebrand, M.S.; Andermann, E.; Andermann, F.; Gambardella, A.; Tinuper, P.; Licchetta, L.; Scheffer, I.E.; Criscuolo, C.; Filla, A.; Ferlazzo, E.; Ahmad, J.; Ahmad, A.; Baykan, B.; Said, E.; Topcu, M.; Riguzzi, P.; King, M.D.; Ozkara, C.; Andrade, D.M.; Engelsen, B.A.; Crespel, A.; Lindenau, M.; Lohmann, E.; Saletti, V.; Massano, J.; Privitera, M.; Espay, A.J.; Kauffmann, B.; Duchowny, M.; Moller, R.S.; Straussberg, R.; Afawi, Z.; Ben-Zeev, B.; Samocha, K.E.; Daly, M.J.; Petrou, S.; Lerche, H.; Palotie, A.; Lehesjoki, A.-E.
Adult patients with intellectual disability and epilepsy: clinical and genetic study of 114 cases
2016 Stipa, Carlotta; Licchetta, Laura; Farolfi, A; Paccagnella, E; Magini, P; Pippucci, T; Leta, C; Menghi, V; Ferri, L; Mostacci, B; Tinuper, Paolo; Bisulli, Francesca
Identification of genes responsible for Nocturnal Frontal Lobe Epilepsy (NFLE): role of DEPDC5 mutations
2016 L. Licchetta; T.Pippucci;S. Baldassari; F.Provini; B.Mostacci; I.Naldi; F.Palombo; P. Magini; M. Seri; F. Bisulli; P. Tinuper; LICE NFLE Study Group
Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy
2016 Coppola, Antonietta; Caccavale, Carmela; Santulli, Lia; Balestrini, Simona; Cagnetti, Claudia; Licchetta, Laura; Esposito, Marcello; Bisulli, Francesca; Tinuper, Paolo; Provinciali, Leandro; Minetti, Carlo; Zara, Federico; Striano, Pasquale; Striano, Salvatore
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2
2016 Henden, Lyndal; Freytag, Saskia; Afawi, Zaid; Baldassari, Sara; Berkovic, Samuel F.; Bisulli, Francesca; Canafoglia, Laura; Casari, Giorgio; Crompton, Douglas Ewan; Depienne, Christel; Gecz, Jozef; Guerrini, Renzo; Helbig, Ingo; Hirsch, Edouard; Keren, Boris; Klein, Karl Martin; Labauge, Pierre; Leguern, Eric; Licchetta, Laura; Mei, Davide; Nava, Caroline; Pippucci, Tommaso; Rudolf, Gabrielle; Scheffer, Ingrid Eileen; Striano, Pasquale; Tinuper, Paolo; Zara, Federico; Corbett, Mark; Bahlo, Melanie
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)
2016 Berkovic, Samuel F; Staropoli, John F.; Carpenter, Stirling; Oliver, Karen L.; Kmoch, Stanislav; Anderson, Glenn W.; Damiano, John A.; Hildebrand, Michael S.; Sims, Katherine B.; Cotman, Susan L.; Bahlo, Melanie; Smith, Katherine R.; Cadieux Dion, Maxime; Cossette, Patrick; Jedličková, Ivana; Přistoupilová, Anna; Mole, Sara E. ANCL Gene Discovery Consortium […; Bisulli, Francesca; Licchetta, Laura; Tinuper, Paolo; ], . .
Definition and diagnostic criteria of sleep-related hypermotor epilepsy
2016 Tinuper, Paolo; Bisulli, Francesca; Cross, J.H.; Hesdorffer, Dale; Kahane, Philippe; Nobili, Lino; Provini, Federica; Scheffer, Ingrid E.; Tassi, Laura; Vignatelli, Luca; Bassetti, Claudio; Cirignotta, Fabio; Derry, Christopher; Gambardella, Antonio; Guerrini, Renzo; Halasz, Peter; Licchetta, Laura; Mahowald, Mark; Manni, Raffaele; Marini, Carla; Mostacci, Barbara; Naldi, Ilaria; Parrino, Liborio; Picard, Fabienne; Pugliatti, Maura; Ryvlin, Philippe; Vigevano, Federico; Zucconi, Marco; Berkovic, Samuel; Ottman, Ruth
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 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 | - |
| 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 | - |
| Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations | Scheffer, Ingrid E; Heron, Sarah E; Regan, Brigid M; Mandelstam, Simone; Crompton, Douglas E; Hod...gson, Bree L; Licchetta, Laura; Provini, Federica; Bisulli, Francesca; Vadlamudi, Lata; Gecz, Jozef; Connelly, Alan; Tinuper, Paolo; Ricos, Michael G; Berkovic, Samuel F; Dibbens, Leanne M | 2014-01-01 | ANNALS OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Limbic encephalitis with anti-GAD antibodies and Thomsen myotonia: A casual or causal association? | Licchetta, L.; Bisulli, F.; Naldi, I.; Mainieri, G.; Tinuper, P. | 2014-01-01 | EPILEPTIC DISORDERS | - | 1.01 Articolo in rivista | - |
| Progressive myoclonic epilepsies: definitive and still undetermined causes | Franceschetti S.; Michelucci R.; Canafoglia L.; Striano P.; Gambardella A.; Magaudda A.; Tinuper ...P.; La Neve A.; Ferlazzo E.; Gobbi G.; Giallonardo A.T.; Capovilla G.; Visani E.; Panzica F.; Avanzini G.; Tassinari C.A.; Bianchi A.; Zara F.; Bisulli F.; Posar A.; Santucci M.; Licchetta L.; (Collaborative LICE study group on PMEs) | 2014-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Tailored surgery for drug-resistant epilepsy due to temporal pole encephalocele and microdysgenesis. | M. Giulioni;L. Licchetta;F. Bisulli;G. Rubboli;B. Mostacci;G. Marucci;M. Martinoni;L. Ferri;L. Vo...lpi;F. Calbucci;A. Baruzzi;P. Tinuper | 2014-01-01 | SEIZURE | - | 1.01 Articolo in rivista | - |
| Response to the letter "New avenues to prevent sudden unexpected death in nocturnal frontal lobe epilepsy: follow the route established by omega-3 polyunsaturated fatty acids". | B. Mostacci;F. Bisulli;L. Vignatelli;L. Licchetta;L. D. Vito;C. Rinaldi;I. Trippi;L. Ferri;G. Pla...zzi;F. Provini;P. Tinuper | 2015-01-01 | SLEEP MEDICINE | - | 1.04 Replica / breve intervento (e simili) | - |
| A prospective study of direct medical costs in a large cohort of consecutively enrolled patients with refractory epilepsy in Italy | Chiara Luoni; Maria Paola Canevini; Giuseppe Capovilla; Giovambattista De Sarro; Carlo Andrea Gal...imberti; Giuliana Gatti; Renzo Guerrini; Angela La Neve; Iolanda Mazzucchelli; Eleonora Rosati; Luigi Maria Specchio; Salvatore Striano; Paolo Tinuper; Emilio Perucca; Study of Outcome of PHarmacoresistance In Epilepsy (SOPHIE) collaborators; Agostino Baruzzi; Erminio Bonizzoni; Cinzia Fattore; Valentina Franco; Ambra Malerba; Mario Marzanatti; Veriano Alexandre Jr; Francesca Beccaria; Francesca Bisulli; Sophie Cagdas; Clotilde Ciampa; Luigi Del Gaudio; Benedetta Frassine; Antonio Gambardella; Simone Gana; Lucio Giordano; Angelo Labate; Francesca La Briola; Marianna Ladogana; Laura Licchetta; Giancarlo Muscas; Anna Maria Papantonio; Angelo Pascarella; Simona Pellacani; Lia Santulli; Pasquale Striano; Salvatore Striano; Alessandra Tiberti; Rossana Tozzi; Marina Trivisano | 2015-01-01 | EPILEPSIA | - | 1.01 Articolo in rivista | - |
| PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy |
Hildebrand M.S.; Tankard R.; Gazina E.V.; Damiano J.A.; Lawrence K.M.;Dahl H-H. M.; Regan B.M.; S...hearer A.E.; Smith R.J.H.; Marini C.; Guerrini R.; Labate A.; Gambardella A.; Tinuper P.; Licchetta L.; Baldassari S.; Bisulli F.; Pippucci T.; Scheffer I.E.; Reid C.A.; Petrou S.; Bahlo M.; Berkovic S.F. |
2015-01-01 | ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY | - | 1.01 Articolo in rivista | acn3.224.pdf |
| Incidence of sudden unexpected death in nocturnal frontal lobe epilepsy: a cohort study. | B. Mostacci;F. Bisulli;L. Vignatelli;L. Licchetta;L. D. Vito;C. Rinaldi;I. Trippi;L. Ferri;G. Pla...zzi;F. Provini;P. Tinuper | 2015-01-01 | SLEEP MEDICINE | - | 1.01 Articolo in rivista | 1-s2.0-S1389945714004894-main.pdf |
| Prevalence of Nocturnal Frontal Lobe Epilepsy in the Adult Population of Bologna and Modena, Emilia-Romagna Region, Italy. | L. Vignatelli;F. Bisulli;G. Giovannini;L. Licchetta;I. Naldi;B. Mostacci;G. Rubboli;F. Provini;P.... Tinuper;S. Meletti | 2015-01-01 | SLEEP | - | 1.01 Articolo in rivista | - |
| A Novel Mutation af Cln3 Associated with Delayed-Classic Juvenile Ceroid Lipofucinois and Autophagic Vacuolar Myopathy | Licchetta, L; Bisulli, F; Fietz, M; Valentino, M L; Morbin, M; Mostacci, B; Oliver, K L; Berkovic..., S F; Tinuper, P | 2015-01-01 | EUROPEAN JOURNAL OF MEDICAL GENETICS | - | 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.pdf; Additional Files.zip |
| A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy | Muona, M.; Berkovic, S.F.; Dibbens, L.M.; Oliver, K.L.; Maljevic, S.; Bayly, M.A.; Joensuu, T.; C...anafoglia, L.; Franceschetti, S.; Michelucci, R.; Markkinen, S.; Heron, S.E.; Hildebrand, M.S.; Andermann, E.; Andermann, F.; Gambardella, A.; Tinuper, P.; Licchetta, L.; Scheffer, I.E.; Criscuolo, C.; Filla, A.; Ferlazzo, E.; Ahmad, J.; Ahmad, A.; Baykan, B.; Said, E.; Topcu, M.; Riguzzi, P.; King, M.D.; Ozkara, C.; Andrade, D.M.; Engelsen, B.A.; Crespel, A.; Lindenau, M.; Lohmann, E.; Saletti, V.; Massano, J.; Privitera, M.; Espay, A.J.; Kauffmann, B.; Duchowny, M.; Moller, R.S.; Straussberg, R.; Afawi, Z.; Ben-Zeev, B.; Samocha, K.E.; Daly, M.J.; Petrou, S.; Lerche, H.; Palotie, A.; Lehesjoki, A.-E. | 2015-01-01 | NATURE GENETICS | - | 1.01 Articolo in rivista | emss-60739.pdf |
| 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 | - |
| Identification of genes responsible for Nocturnal Frontal Lobe Epilepsy (NFLE): role of DEPDC5 mutations | L. Licchetta; T.Pippucci;S. Baldassari; F.Provini; B.Mostacci; I.Naldi; F.Palombo; P. Magini; M. ...Seri; F. Bisulli; P. Tinuper; LICE NFLE Study Group | 2016-01-01 | CLINICAL CASES AND REVIEWS IN EPILEPSY | - | 1.01 Articolo in rivista | - |
| Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy | Coppola, Antonietta; Caccavale, Carmela; Santulli, Lia; Balestrini, Simona; Cagnetti, Claudia; Li...cchetta, Laura; Esposito, Marcello; Bisulli, Francesca; Tinuper, Paolo; Provinciali, Leandro; Minetti, Carlo; Zara, Federico; Striano, Pasquale; Striano, Salvatore | 2016-01-01 | EPILEPSY & BEHAVIOR | - | 1.01 Articolo in rivista | - |
| Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2 | Henden, Lyndal; Freytag, Saskia; Afawi, Zaid; Baldassari, Sara; Berkovic, Samuel F.; Bisulli, Fra...ncesca; Canafoglia, Laura; Casari, Giorgio; Crompton, Douglas Ewan; Depienne, Christel; Gecz, Jozef; Guerrini, Renzo; Helbig, Ingo; Hirsch, Edouard; Keren, Boris; Klein, Karl Martin; Labauge, Pierre; Leguern, Eric; Licchetta, Laura; Mei, Davide; Nava, Caroline; Pippucci, Tommaso; Rudolf, Gabrielle; Scheffer, Ingrid Eileen; Striano, Pasquale; Tinuper, Paolo; Zara, Federico; Corbett, Mark; Bahlo, Melanie | 2016-01-01 | HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease) | Berkovic, Samuel F; Staropoli, John F.; Carpenter, Stirling; Oliver, Karen L.; Kmoch, Stanislav; ...Anderson, Glenn W.; Damiano, John A.; Hildebrand, Michael S.; Sims, Katherine B.; Cotman, Susan L.; Bahlo, Melanie; Smith, Katherine R.; Cadieux Dion, Maxime; Cossette, Patrick; Jedličková, Ivana; Přistoupilová, Anna; Mole, Sara E. ANCL Gene Discovery Consortium […; Bisulli, Francesca; Licchetta, Laura; Tinuper, Paolo; ], . . | 2016-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Definition and diagnostic criteria of sleep-related hypermotor epilepsy | Tinuper, Paolo; Bisulli, Francesca; Cross, J.H.; Hesdorffer, Dale; Kahane, Philippe; Nobili, Lino...; Provini, Federica; Scheffer, Ingrid E.; Tassi, Laura; Vignatelli, Luca; Bassetti, Claudio; Cirignotta, Fabio; Derry, Christopher; Gambardella, Antonio; Guerrini, Renzo; Halasz, Peter; Licchetta, Laura; Mahowald, Mark; Manni, Raffaele; Marini, Carla; Mostacci, Barbara; Naldi, Ilaria; Parrino, Liborio; Picard, Fabienne; Pugliatti, Maura; Ryvlin, Philippe; Vigevano, Federico; Zucconi, Marco; Berkovic, Samuel; Ottman, Ruth | 2016-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | 1834.full.pdf; supp_WNL.0000000000002666_Appendix_e-1.pdf |
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