ZARA, FEDERICO

ZARA, FEDERICO  

100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftamologia, Genetica e Scienze Materno-Infantili  

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(1)H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. 1-gen-2009 Striano, Pasquale; Caranci, F.; Benedetto, R. D.; Tortora, F.; Zara, F.; Striano, S.
17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome 1-gen-2016 Bernardo, P.; Madia, F.; Santulli, L.; Del Gaudio, L.; Caccavale, C.; Zara, F.; Traverso, M.; Cirillo, M.; Striano, S.; Coppola, A.
22-year-old girl with status epilepticus and progressive neurological symptoms. 1-gen-2009 Striano, Pasquale; Ackerley, C. A.; Cervasio, M.; Girard, J.; Turnbull, J.; Del, M. L.; Striano, S.; Zara, F.; Minassian, B. A.
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 1-gen-2006 Elia, M.; Striano, Pasquale; Fichera, M.; Gaggero, R.; Castiglia, L.; Galesi, O.; Malacarne, M.; Pierluigi, M.; Amato, C.; Musumeci, S. A.; Romano, C.; Majore, S.; Grammatico, P.; Zara, F.; Striano, S.; Faravelli, F.
A clinical and genetic study of 33 new cases with early-onset absence epilepsy. 1-gen-2011 Giordano, L; Vignoli, A; Accorsi, P; Galli, J; Pezzella, Marianna; Traverso, M; Battaglia, S; Baglietto, MARIA GIUSEPPINA; Beccaria, F; Cerminara, C; Gambara, S; Del Giudice, E; Crichiutti, G; Bisulli, F; Pinci, M; Tinuper, P; Briatore, E; Calzolari, S; Coppola, A; Canevini, Mp; Capovilla, G; Striano, S; Zara, F; Minetti, Carlo; Striano, Pasquale
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 1-gen-2010 Coppola, A.; Striano, Pasquale; Gimelli, S.; Ciampa, C.; Santulli, L.; Caranci, F.; Zuffardi, O.; Gimelli, G.; Striano, S.; Zara, F.
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy. 1-gen-2011 Manna, I.; Gambardella, A.; Bianchi, A.; Striano, Pasquale; Tozzi, R.; Aguglia, U.; Beccaria, F.; Benna, P.; Campostrini, R.; Canevini, M. P.; Condino, F.; Durisotti, C.; Elia, M.; Giallonardo, A. T.; Iudice, A.; Labate, A.; Neve, A. L.; Michelucci, R.; Muscas, G. C.; Paravidino, R.; Zaccara, G.; Zucca, C.; Zara, F.; Perucca, E.
A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy 1-gen-2006 Cassandrini, D; Calevo, Mg; Tessa, A; Manfredi, G; Fattori, F; Meschini, Mc; Carrozzo, R; Tonoli, E; Pedemonte, M; Minetti, Carlo; Zara, F; Santorelli, Fm; Bruno, C.
A novel SCN2A mutation in family with benign familial infantile seizures. 1-gen-2006 Striano, Pasquale; Bordo, L.; Lispi, M. L.; Specchio, N.; Minetti, Carlo; Vigevano, F.; Zara, F.
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 1-gen-2011 Italiano, D.; Pezzella, M.; Coppola, A.; Magaudda, A.; Ferlazzo, E.; Bramanti, P.; Striano, S.; Zara, F.; Striano, Pasquale
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 1-gen-2008 Striano, Pasquale; Sofia, V.; Capovilla, G.; Rubboli, G.; Bonaventura, C. D.; Coppola, A.; Vitale, G.; Fontanillas, L.; Giallonardo, A. T.; Biondi, R.; Romeo, A.; Viri, M.; Zara, F.; Striano, S.
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies 1-gen-2018 Carvill, G. L.; Engel, K. L.; Ramamurthy, A.; Cochran, J. N.; Roovers, J.; Stamberger, H.; Lim, N.; Schneider, A. L.; Hollingsworth, G.; Holder, D. H.; Regan, B. M.; Lawlor, J.; Lagae, L.; Ceulemans, B.; Bebin, E. M.; Nguyen, J.; Striano, P.; Zara, F.; Helbig, I.; Moller, R. S.; von Spiczak, S.; Muhle, H.; Caglayan, H.; Sterbova, K.; Craiu, D.; Hoffman, D.; Lehesjoki, A. -E.; Selmer, K.; Depienne, C.; Lemke, J.; Marini, C.; Guerrini, R.; Neubauer, B.; Talvik, T.; Leguern, E.; de Jonghe, P.; Weckhuysen, S.; Barsh, G. S.; Weckhuysen, S.; Meisler, M.; Berkovic, S. F.; De Jonghe, P.; Scheffer, I. E.; Myers, R. M.; Cooper, G. M.; Mefford, H. C.
Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy 1-gen-2003 Nabbout, R.; Kozlovski, A.; Gennaro, E.; Bahi-Buisson, N.; Zara, F.; Chiron, C.; Bianchi, A.; Brice, A.; Leguern, E.; Dulac, O.
Addition of verapamil in the treatment of severe myoclonic epilepsy in infancy 1-gen-2009 Iannetti, P.; Parisi, P.; Spalice, A.; Ruggieri, M.; Zara, F.
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 1-gen-2020 Scala, M.; Bianchi, A.; Bisulli, F.; Coppola, A.; Elia, M.; Trivisano, M.; Pruna, D.; Pippucci, T.; Canafoglia, L.; Lattanzi, S.; Franceschetti, S.; Nobile, C.; Gambardella, A.; Michelucci, R.; Zara, F.; Striano, P
AIMP1/p43 mutation and PMLD 1-gen-2011 Biancheri, R.; Rossi, A.; Zara, F.; Filocamo, M.
Alterations in the alfa(2) gamma ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies 1-gen-2017 Santolini, Ines; Celli, Roberta; Cannella, Milena; Imbriglio, Tiziana; Guiducci, Michela; Parisi, Pasquale; Schubert, Julian; Iacomino, Michele; Zara, Federico; Lerche, Holger; Moyanova, Slavianka; Ngomba, Richard Teke; van Luijtelaar, Gilles; Battaglia, Giuseppe; Bruno, Valeria; Striano, Pasquale; Nicoletti, Ferdinando; Palotie, Aarno; Folkhälsan, Anna-Elina Lehesjoki; Ruppert, Ann-Kathrin; Siren, Auli; Koeleman, Bobby; Lal, Dennis; Becker, Felicitas; Caglayan, Hande; Hjalgrim, Helle; Muhle, Hiltrud; Thiele, Holger; Helbig, Ingo; Altmuller, Janine; Jabbari, Kamel; Everett, Kate; May, Patrick; Nurnberg, Peter; Møller, Rikke; Nabbout, Rima; Krause, Roland; Balling, Rudi; Baulac, Stephanie; Sander, Thomas; Kunz, Wolfram; Weber, Yvonne; Bianchi, Amedeo; La Neve, Angela; Coppola, Antonietta; Striano, Salvatore; Capovilla, Giuseppe; Ferlazzo, Edoardo; Bagnasco, Irene; Ferretti, Alessandro; Di Bonaventura, Carlo; Vari, Maria Stella; Pinto, Francesca; Bisulli, Francesca; Tinuper, Paolo; Minetti, Carlo; Belcastro, Vincenzo; Giordano, Lucio; Gambardella, Antonio
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 1-gen-2019 Salpietro, V; Dixon, Cl; Guo, H; Bello, Od; Vandrovcova, J; Efthymiou, S; Maroofian, R; Heimer, G; Burglen, L; Valence, S; Torti, E; Hacke, M; Rankin, J; Tariq, H; Colin, E; Procaccio, V; Striano, P; Mankad, K; Lieb, A; Chen, S; Pisani, L; Bettencourt, C; Männikkö, R; Manole, A; Brusco, A; Grosso, E; Ferrero, Gb; Armstrong-Moron, J; Gueden, S; Bar-Yosef, O; Tzadok, M; Monaghan, Kg; Santiago-Sim, T; Person, Re; Cho, Mt; Willaert, R; Yoo, Y; Chae, Jh; Quan, Y; Wu, H; Wang, T; Bernier, Ra; Xia, K; Blesson, A; Jain, M; Motazacker, Mm; Jaeger, B; Schneider, Al; Boysen, K; Muir, Am; Myers, Ct; Gavrilova, Rh; Gunderson, L; Schultz-Rogers, L; Klee, Ew; Dyment, D; Osmond, M; Parellada, M; Llorente, C; Gonzalez-Peñas, J; Carracedo, A; Van Haeringen, A; Ruivenkamp, C; Nava, C; Heron, D; Nardello, R; Iacomino, M; Minetti, C; Skabar, A; Fabretto, A; SYNAPS Study, Group; Raspall-Chaure, M; Chez, M; Tsai, A; Fassi, E; Shinawi, M; Constantino, Jn; De Zorzi, R; Fortuna, S; Kok, F; Keren, B; Bonneau, D; Choi, M; Benzeev, B; Zara, F; Mefford, Hc; Scheffer, Ie; Clayton-Smith, J; Macaya, A; Rothman, Je; Eichler, Ee; Kullmann, Dm; Houlden, H; Hanna, Mg; Bugiardini, E; Hostettler, I; O'Callaghan, B; Khan, A; Cortese, A; O'Connor, E; Yau, Wy; Bourinaris, T; Kaiyrzhanov, R; Chelban, V; Madej, M; Diana, Mc; Vari, Ms; Pedemonte, M; Bruno, C; Balagura, G; Scala, M; Fiorillo, C; Nobili, L; Malintan, Nt; Zanetti, Mn; Krishnakumar, Ss; Lignani, G; Jepson, Jec; Broda, P; Baldassari, S; Rossi, P; Fruscione, F; Madia, F; Traverso, M; De-Marco, P; Pérez-Dueñas, B; Munell, F; Kriouile, Y; El-Khorassani, M; Karashova, B; Avdjieva, D; Kathom, H; Tincheva, R; Van-Maldergem, L; Nachbauer, W; Boesch, S; Gagliano, A; Amadori, E; Goraya, Js; Sultan, T; Kirmani, S; Ibrahim, S; Jan, F; Mine, J; Banu, S; Veggiotti, P; Zuccotti, Gv; Ferrari, Md; Van Den Maagdenberg, Amj; Verrotti, A; Marseglia, Gl; Savasta, S; Soler, Ma; Scuderi, C; Borgione, E; Chimenz, R; Gitto, E; Dipasquale, V; Sallemi, A; Fusco, M; Cuppari, C; Cutrupi, Mc; Ruggieri, M; Cama, A; Capra, V; Mencacci, Ne; Boles, R; Gupta, N; Kabra, M; Papacostas, S; Zamba-Papanicolaou, E; Dardiotis, E; Maqbool, S; Rana, N; Atawneh, O; Lim, Sy; Shaikh, F; Koutsis, G; Breza, M; Coviello, Da; Dauvilliers, Ya; Alkhawaja, I; Alkhawaja, M; Al-Mutairi, F; Stojkovic, T; Ferrucci, V; Zollo, M; Alkuraya, Fs; Kinali, M; Sherifa, H; Benrhouma, H; Turki, Iby; Tazir, M; Obeid, M; Bakhtadze, S; Saadi, Nw; Zaki, Ms; Triki, Cc; Benfenati, F; Gustincich, S; Kara, M; Belcastro, V; Specchio, N; Capovilla, G; Karimiani, Eg; Salih, Am; Okubadejo, Nu; Ojo, Oo; Oshinaike, Oo; Oguntunde, O; Wahab, K; Bello, Ah; Abubakar, S; Obiabo, Y; Nwazor, E; Ekenze, O; Williams, U; Iyagba, A; Taiwo, L; Komolafe, M; Senkevich, K; Shashkin, C; Zharkynbekova, N; Koneyev, K; Manizha, G; Isrofilov, M; Guliyeva, U; Salayev, K; Khachatryan, S; Rossi, S; Silvestri, G; Haridy, N; Ramenghi, La; Xiromerisiou, G; David, E; Aguennouz, M; Fidani, L; Spanaki, C; Tucci, A.
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 1-gen-2007 Striano, Pasquale; Coppola, A.; Pezzella, M.; Ciampa, C.; Specchio, N.; Ragona, F.; Mancardi, M. M.; Gennaro, E.; Beccaria, F.; Capovilla, G.; Rasmini, P.; Besana, D.; Coppola, G. G.; Elia, M.; Granata, T.; Vecchi, M.; Vigevano, F.; Viri, M.; Gaggero, R.; Striano, S.; Zara, F.
Analysis of shared heritability in common disorders of the brain 1-gen-2018 Erneri, Anttila; Brendan, Bulik-Sullivan; Hilary, K Finucane; Raymond, K Walters; Jose, Bras; Laramie, Duncan; Valentina, Escott-Price; Guido, J Falcone; Padhraig, Gormley; Rainer, Malik; Nikolaos, A Patsopoulos; Stephan, Ripke; Zhi, Wei; Dongmei, Yu; Phil, H Lee; Patrick, Turley; Benjamin, Grenier-Boley; Vincent, Chouraki; Yoichiro, Kamatani; Claudine, Berr; Luc, Letenneur; Didier, Hannequin; Philippe, Amouyel; Anne, Boland; Jean-Francois, Deleuze; Emmanuelle, Duron; Badri, N Vardarajan; Christiane, Reitz; Alison, M Goate; Matthew, J Huentelman; M Ilyas Kamboh, ; Eric, B Larson; Ekaterina, Rogaeva; Peter St George-Hyslop, ; Hakon, Hakonarson; Walter, A Kukull; Lindsay, A Farrer; Lisa, L Barnes; Thomas, G Beach; F Yesim Demirci, ; Elizabeth, Head; Christine, M Hulette; Gregory, A Jicha; John SK Kauwe, ; Jeffrey, A Kaye; James, B Leverenz; Allan, I Levey; Andrew, P Lieberman; Vernon, S Pankratz; Wayne, W Poon; Joseph, F Quinn; Andrew, J Saykin; Lon, S Schneider; Amanda, G Smith; Joshua, A Sonnen; Robert, A Stern; Vivianna, M Van Deerlin; Linda, J Van Eldik; Denise, Harold; Giancarlo, Russo; David, C Rubinsztein; Anthony, Bayer; Magda, Tsolaki; Petra, Proitsi; Nick, C Fox; Harald, Hampel; Michael, J Owen; Simon, Mead; Peter, Passmore; Kevin, Morgan; Markus, M Nöthen; Jonathan, M Schott; Martin, Rossor; Michelle, K Lupton; Per, Hoffmann; Johannes, Kornhuber; Brian, Lawlor; Andrew, Mcquillin; Ammar, Al-Chalabi; Joshua, C Bis; Agustin, Ruiz; Mercè, Boada; Sudha, Seshadri; Alexa, Beiser; Kenneth, Rice; Sven, J van der Lee; Philip, L De Jager; Daniel, H Geschwind; Matthias, Riemenschneider; Steffi, Riedel-Heller; Jerome, I Rotter; Gerhard, Ransmayr; Bradley, T Hyman; Carlos, Cruchaga; Montserrat, Alegret; Bendik, Winsvold; Priit, Palta; Kai-How, Farh; Ester, Cuenca-Leon; Nicholas, Furlotte; Tobias, Kurth; Lannie, Ligthart; Gisela, M Terwindt; Tobias, Freilinger; Caroline, Ran; Scott, D Gordon; Guntram, Borck; Hieab HH Adams, ; Terho, Lehtimäki; Juho, Wedenoja; Julie, E Buring; Markus, Schürks; Maria, Hrafnsdottir; Jouke-Jan, Hottenga; Brenda, Penninx; Ville, Artto; Mari, Kaunisto; Salli, Vepsäläinen; Nicholas, G Martin; Grant, W Montgomery; Mitja, I Kurki; Eija, Hämäläinen; Hailiang, Huang; Jie, Huang; Cynthia, Sandor; Striano, Pasquale; Zara, Federico; Caleb, Webber; Bertram, Muller-Myhsok; Stefan, Schreiber; Veikko, Salomaa; Elizabeth, Loehrer; Hartmut, Göbel; Alfons, Macaya; Patricia, Pozo-Rosich; Thomas, Hansen; Thomas, Werge; Jaakko, Kaprio; Andres, Metspalu; Striano, Pasquale; Zara, Federico; Christian, Kubisch; Michel, D Ferrari; Andrea, C Belin; Arn MJM van den Maagdenberg, ; John-Anker, Zwart; Dorret, Boomsma; Nicholas, Eriksson; Jes, Olesen; Daniel, I Chasman; Dale, R Nyholt; Richard, Anney; Andreja, Avbersek; Larry, Baum