Baldassari S.; Picard F.; Verbeek N.E.; van Kempen M.; Brilstra E.H.; Lesca G.; Conti V.; Guerrini R.; Bisulli F.; Licchetta L.; Pippucci T.; Tinuper P.; Hirsch E.; de Saint Martin A.; Chelly J.; Rudolf G.; Chipaux M.; Ferrand-Sorbets S.; Dorfmuller G.; Sisodiya S.; Balestrini S.; Schoeler N.; Hernandez-Hernandez L.; Krithika S.; Oegema R.; Hagebeuk E.; Gunning B.; Deckers C.; Berghuis B.; Wegner I.; Niks E.; Jansen F.E.; Braun K.; de Jong D.; Rubboli G.; Talvik I.; Sander V.; Uldall P.; Jacquemont M.-L.; Nava C.; Leguern E.; Julia S.; Gambardella A.; d'Orsi G.; Crichiutti G.; Faivre L.; Darmency V.; Benova B.; Krsek P.; Biraben A.; Lebre A.-S.; Jennesson M.; Sattar S.; Marchal C.; Nordli D.R.; Lindstrom K.; Striano P.; Lomax L.B.; Kiss C.; Bartolomei F.; Lepine A.F.; Schoonjans A.-S.; Stouffs K.; Jansen A.; Panagiotakaki E.; Ricard-Mousnier B.; Thevenon J.; de Bellescize J.; Catenoix H.; Dorn T.; Zenker M.; Muller-Schluter K.; Brandt C.; Krey I.; Polster T.; Wolff M.; Balci M.; Rostasy K.; Achaz G.; Zacher P.; Becher T.; Cloppenborg T.; Yuskaitis C.J.; Weckhuysen S.; Poduri A.; Lemke J.R.; Moller R.S.; Baulac S., The landscape of epilepsy-related GATOR1 variants, «GENETICS IN MEDICINE», 2019, 21, pp. 398 - 408 [Scientific article]
Francesca Bisulli, Lorenzo Muccioli, Giuseppe d’Orsi, Laura Canafoglia, Elena Freri, Laura Licchetta, Barbara Mostacci, Patrizia Riguzzi, Federica Pondrelli, Carlo Avolio, Tommaso Martino, Roberto Michelucci, Paolo Tinuper, Treatment with metformin in twelve patients with Lafora disease, «ORPHANET JOURNAL OF RARE DISEASES», 2019, 14, pp. 1 - 5 [Scientific article]Open Access
Feng Y.-C.A.; Howrigan D.P.; Abbott L.E.; Tashman K.; Cerrato F.; Singh T.; Heyne H.; Byrnes A.; Churchhouse C.; Watts N.; Solomonson M.; Lal D.; Heinzen E.L.; Dhindsa R.S.; Stanley K.E.; Cavalleri G.L.; Hakonarson H.; Helbig I.; Krause R.; May P.; Weckhuysen S.; Petrovski S.; Kamalakaran S.; Sisodiya S.M.; Cossette P.; Cotsapas C.; De Jonghe P.; Dixon-Salazar T.; Guerrini R.; Kwan P.; Marson A.G.; Stewart R.; Depondt C.; Dlugos D.J.; Scheffer I.E.; Striano P.; Freyer C.; McKenna K.; Regan B.M.; Bellows S.T.; Leu C.; Bennett C.A.; Johns E.M.C.; Macdonald A.; Shilling H.; Burgess R.; Weckhuysen D.; Bahlo M.; O'Brien T.J.; Todaro M.; Stamberger H.; Andrade D.M.; Sadoway T.R.; Mo K.; Krestel H.; Gallati S.; Papacostas S.S.; Kousiappa I.; Tanteles G.A.; Sterbova K.; Vlckova M.; Sedlackova L.; Lassuthova P.; Klein K.M.; Rosenow F.; Reif P.S.; Knake S.; Kunz W.S.; Zsurka G.; Elger C.E.; Bauer J.; Rademacher M.; Pendziwiat M.; Muhle H.; Rademacher A.; van Baalen A.; von Spiczak S.; Stephani U.; Afawi Z.; Korczyn A.D.; Kanaan M.; Canavati C.; Kurlemann G.; Muller-Schluter K.; Kluger G.; Hausler M.; Blatt I.; Lemke J.R.; Krey I.; Weber Y.G.; Wolking S.; Becker F.; Hengsbach C.; Rau S.; Maisch A.F.; Steinhoff B.J.; Schulze-Bonhage A.; Schubert-Bast S.; Schreiber H.; Borggrafe I.; Schankin C.J.; Mayer T.; Korinthenberg R.; Brockmann K.; Dennig D.; Madeleyn R.; Kalviainen R.; Auvinen P.; Saarela A.; Linnankivi T.; Lehesjoki A.-E.; Rees M.I.; Chung S.-K.; Pickrell W.O.; Powell R.; Schneider N.; Balestrini S.; Zagaglia S.; Braatz V.; Johnson M.R.; Auce P.; Sills G.J.; Baum L.W.; Sham P.C.; Cherny S.S.; Lui C.H.T.; Barisic N.; Delanty N.; Doherty C.P.; Shukralla A.; McCormack M.; El-Naggar H.; Canafoglia L.; Franceschetti S.; Castellotti B.; Granata T.; Zara F.; Iacomino M.; Madia F.; Vari M.S.; Mancardi M.M.; Salpietro V.; Bisulli F.; Tinuper P.; Licchetta L.; Pippucci T.; Stipa C.; Minardi R.; Gambardella A.; Labate A.; Annesi G.; Manna L.; Gagliardi M.; Parrini E.; Mei D.; Vetro A.; Bianchini C.; Montomoli M.; Doccini V.; Marini C.; Suzuki T.; Inoue Y.; Yamakawa K.; Tumiene B.; Sadleir L.G.; King C.; Mountier E.; Caglayan S.H.; Arslan M.; Yapici Z.; Yis U.; Topaloglu P.; Kara B.; Turkdogan D.; Gundogdu-Eken A.; Bebek N.; Ugur-Iseri S.; Baykan B.; Salman B.; Haryanyan G.; Yucesan E.; Kesim Y.; Ozkara C.; Poduri A.; Shiedley B.R.; Shain C.; Buono R.J.; Ferraro T.N.; Sperling M.R.; Lo W.; Privitera M.; French J.A.; Schachter S.; Kuzniecky R.I.; Devinsky O.; Hegde M.; Khankhanian P.; Helbig K.L.; Ellis C.A.; Spalletta G.; Piras F.; Piras F.; Gili T.; Ciullo V.; Reif A.; McQuillin A.; Bass N.; McIntosh A.; Blackwood D.; Johnstone M.; Palotie A.; Pato M.T.; Pato C.N.; Bromet E.J.; Carvalho C.B.; Achtyes E.D.; Azevedo M.H.; Kotov R.; Lehrer D.S.; Malaspina D.; Marder S.R.; Medeiros H.; Morley C.P.; Perkins D.O.; Sobell J.L.; Buckley P.F.; Macciardi F.; Rapaport M.H.; Knowles J.A.; Fanous A.H.; McCarroll S.A.; Gupta N.; Gabriel S.B.; Daly M.J.; Lander E.S.; Lowenstein D.H.; Goldstein D.B.; Lerche H.; Berkovic S.F.; Neale B.M., Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals, «AMERICAN JOURNAL OF HUMAN GENETICS», 2019, 105, pp. 267 - 282 [Scientific article]
Rahel T. Florian, Florian Kraft, Elsa Leitão, Sabine Kaya, Stephan Klebe, Eloi Magnin, Anne-Fleur van Rootselaar, Julien Buratti, Theresa Kühnel, Christopher Schröder, Sebastian Giesselmann, Nikolai Tschernoster, Janine Altmueller, Anaide Lamiral, Boris Keren, Caroline Nava, Delphine Bouteiller, Sylvie Forlani, Ludmila Jornea, Regina Kubica, Tao Ye, Damien Plassard, Bernard Jost, Vincent Meyer, Jean-François Deleuze, Yannick Delpu, Mario D.M. Avarello, Lisanne S. Vijfhuizen, Gabrielle Rudolf, Edouard Hirsch, Thessa Kroes, Philipp S. Reif, Felix Rosenow, Christos Ganos, Marie Vidailhet, Lionel Thivard, Alexandre Mathieu, Thomas Bourgeron, Ingo Kurth, Haloom Rafehi, Laura Steenpass, Bernhard Horsthemke, FAME consortium, Eric LeGuern, Karl Martin Klein, Pierre Labauge, Mark F. Bennett, Melanie Bahlo, Jozef Gecz, Mark A. Corbett, Marina A.J. Tijssen, Arn M.J.M. van den Maagdenberg, Christel Depienne, Francesca Bisulli, Laura Licchetta, Paolo Tinuper, Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3, «NATURE COMMUNICATIONS», 2019, 10, pp. 1 - 14 [Scientific article]Open Access
Evangelisti, Stefania; Testa, Claudia; Ferri, Lorenzo; Gramegna, Laura Ludovica; Manners, David Neil; Rizzo, Giovanni; Remondini, Daniel; Castellani, Gastone; Naldi, Ilaria; Bisulli, Francesca; Tonon, Caterina; Tinuper, Paolo; Lodi, Raffaele, Brain functional connectivity in sleep-related hypermotor epilepsy, «NEUROIMAGE. CLINICAL», 2018, 17, pp. 873 - 881 [Scientific article]Open Access
Tomson T, Battino D, Bonizzoni E, Craig J, Lindhout D, Perucca E, Sabers A, Thomas SV, Vajda F; EURAP Study Group; Bisulli F; Tinuper P, Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry, «LANCET NEUROLOGY», 2018, 17, pp. 530 - 538 [Scientific article]
Licchetta, Laura; Bisulli, Francesca; Ferri, Lorenzo; Cantalupo, Gaetano; Alvisi, Lara; Vignatelli, Luca; Loddo, Giuseppe; Provini, Federica; Tinuper, Paolo, Cortical myoclonic tremor induced by fixation-off sensitivity: An unusual cause of insomnia, «NEUROLOGY», 2018, 91, pp. 1061 - 1063 [Scientific article]
Manuela Contin, Francesca Bisulli,| Margherita Santucci, Roberto Riva,| Francesca Tonon, Susan Mohamed, Lorenzo Ferri, Carlotta Stipa, Paolo Tinuper, on behalf of the Perampanel Study Group*, A. Parmeggiani, L. Licchetta, Effect of valproic acid on perampanel pharmacokinetics in patients with epilepsy., «EPILEPSIA», 2018, 59, pp. e103 - e108 [Scientific article]
Mostacci, Barbara; Bisulli, Francesca; Poluzzi, Elisabetta; Cocchi, Guido; Piccinni, Carlo; Curti, Alessandra; Simonazzi, Giuliana; Astolfi, Gianni; Rizzo, Nicola; Zenesini, Corrado; D'Alessandro, Roberto; Tinuper, Paolo; Licchetta, Laura, Emilia-Romagna Study on Pregnancy and Exposure to Antiepileptic drugs (ESPEA): a population-based study on prescription patterns, pregnancy outcomes and fetal health, «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2018, 89, pp. 983 - 988 [Scientific article]Open Access
Bisulli, Francesca; Menghi, Veronica; Vignatelli, Luca; Licchetta, Laura; Zenesini, Corrado; Stipa, Carlotta; Morigi, Francesca; Gizzi, Matteo; Avoni, Patrizia; Provini, Federica; Mostacci, Barbara; D'Orsi, Giuseppe; Pippucci, Tommaso; Muccioli, Lorenzo; Tinuper, Paolo, Epilepsy with auditory features: Long-term outcome and predictors of terminal remission, «EPILEPSIA», 2018, 59, pp. 834 - 843 [Scientific article]
Mostacci, Barbara*; Esposto, Roberta; Lello, Stefano; Bisulli, Francesca; Licchetta, Laura; Tinuper, Paolo, Estrogen-related seizure exacerbation following hormone therapy for assisted reproduction in women with epilepsy, «SEIZURE», 2018, 61, pp. 200 - 202 [Scientific article]
McCormack, Mark; Gui, Hongsheng; Ingason, Andrés; Speed, Doug; Wright, Galen E B; Zhang, Eunice J.; Secolin, Rodrigo; Yasuda, Clarissa; Kwok, Maxwell; Wolking, Stefan; Becker, Felicitas; Rau, Sarah; Avbersek, Andreja; Heggeli, Kristin; Leu, Costin; Depondt, Chantal; Sills, Graeme J.; Marson, Anthony G.; Auce, Pauls; Brodie, Martin J.; Francis, Ben; Johnson, Michael R.; Koeleman, Bobby P C; Striano, Pasquale; Coppola, Antonietta; Zara, Federico; Kunz, Wolfram S.; Sander, Josemir W.; Lerche, Holger; Klein, Karl Martin; Weckhuysen, Sarah; Krenn, Martin; Gudmundsson, Lárus J; Stefánsson, Kári; Krause, Roland; Shear, Neil; Ross, Colin J D; Delanty, Norman; Pirmohamed, Munir; Carleton, Bruce C.; Cendes, Fernando; Lopes-Cendes, Iscia; Liao, Wei-Ping; O'Brien, Terence J.; Sisodiya, Sanjay M.; Cherny, Stacey; Kwan, Patrick; Baum, Larry; Cavalleri, Gianpiero L.; International League Against Epilepsy Consortium on Complex Epilepsies; Bisulli, Francesca, Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients, «NEUROLOGY», 2018, 90, pp. e332 - e341 [Scientific article]
Muccioli, Lorenzo; Licchetta, Laura; Stipa, Carlotta; Tinuper, Paolo; Bisulli, Francesca, Juvenile absence epilepsy relapsing as recurrent absence status, mimicking transient global amnesia, in an elderly patient, «EPILEPTIC DISORDERS», 2018, 20, pp. 557 - 561 [Scientific article]
Baldini, Tommaso; Loddo, Giuseppe; Mignani, Francesco; Licchetta, Laura; Bisulli, Francesca; Tinuper, Paolo; Provini, Federica*, Nocturnal motor behaviors with unexpected EEG and brain MRI findings, «SLEEP MEDICINE», 2018, 52, pp. 116 - 117 [Comment or similar]
Di Vito, Lidia; Licchetta, Laura; Pippucci, Tommaso; Baldassari, Sara; Stipa, Carlotta; Mostacci, Barbara; Alvisi, Lara; Tinuper, Paolo; Bisulli, Francesca, Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations, «EPILEPSY & BEHAVIOR», 2018, 79, pp. 169 - 173 [Scientific article]
