المؤلفون: Battaglia, Domenica, Chieffo, Daniela, Lucibello, Simona, Marini, Carla, Sibilia, Valentina, Mei, Davide, Darra, Francesca, Offredi, Francesca, Fontana, Elena, Specchio, Nicola, Cappelletti, Simona, Granata, Tiziana, Ragona, Francesca, Patrini, Mara, Baglietto, Maria G, Prato, Giulia, Ferrari, Annarita, Vigevano, Federico, Mercuri, Eugenio, Bernardina, Bernardo Dalla, Guerrini, Renzo, Dravet, Charlotte, Guzzetta, Francesco

المساهمون: Battaglia, Domenica, Chieffo, Daniela, Lucibello, Simona, Marini, Carla, Sibilia, Valentina, Mei, Davide, Darra, Francesca, Offredi, Francesca, Fontana, Elena, Specchio, Nicola, Cappelletti, Simona, Granata, Tiziana, Ragona, Francesca, Patrini, Mara, Baglietto, Maria G, Prato, Giulia, Ferrari, Annarita, Vigevano, Federico, Mercuri, Eugenio, Bernardina, Bernardo Dalla, Guerrini, Renzo, Dravet, Charlotte, Guzzetta, Francesco

مصطلحات موضوعية: Dravet syndrome, Neurodevelopmental trajectory, Neuropsychological longitudinal study, SCN1A mutation, Visuomotor defects

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33478845; info:eu-repo/semantics/altIdentifier/wos/WOS:000617030200009; volume:43; issue:3; firstpage:419; lastpage:430; numberofpages:12; journal:BRAIN & DEVELOPMENT; https://hdl.handle.net/11562/1038770Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85099628852

الإتاحة: https://doi.org/10.1016/j.braindev.2020.10.004Test
https://hdl.handle.net/11562/1038770Test

المؤلفون: Moller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., van Kempen, Marjan J. A., Klinkenberg, Sylvia, Andrews, Ian, Kelley, Kent, Ronen, Gabriel M., Callen, David, McMahon, Jacinta M., Yendle, Simone C., Carvill, Gemma L., Mefford, Heather C., Nabbout, Rima, Poduri, Annapurna, Striano, Pasquale, Baglietto, Maria G., Zara, Federico, Smith, Nicholas J., Pridmore, Clair, Gardella, Elena, Nikanorova, Marina, Dahl, Hans Atli, Gellert, Pia, Scheffer, Ingrid E., Gunning, Boudewijn, Kragh-Olsen, Bente, Dibbens, Leanne M.

المصدر: Moller , R S , Heron , S E , Larsen , L H G , Lim , C X , Ricos , M G , Bayly , M A , van Kempen , M J A , Klinkenberg , S , Andrews , I , Kelley , K , Ronen , G M , Callen , D , McMahon , J M , Yendle , S C , Carvill , G L , Mefford , H C , Nabbout , R , Poduri , A , Striano , P , Baglietto , M G , Zara , F ....

مصطلحات موضوعية: KCNT1, Autosomal dominant nocturnal frontal lobe epilepsy, Epileptic encephalopathy, Cardiac arrhythmia, Sudden unexpected death in epilepsy

الإتاحة: https://doi.org/10.1111/epi.13071Test
https://cris.maastrichtuniversity.nl/en/publications/03d8cf1d-c65f-465d-9dcd-548b6ae4510dTest

المؤلفون: Nobili, Lino, Baglietto, Maria G., Beelke, Manolo, De Carli, Fabrizio, Di Comite, Raffaella, Fiocchi, Isabella, Rizzo, Pierpaolo, Veneselli, Edvige, Savoini, Margherita, Zanotto, Elisabetta, Ferrillo, Franco

المصدر: Sleep ; volume 27, issue 8, page 1553-1559 ; ISSN 1550-9109 0161-8105

مصطلحات موضوعية: Physiology (medical), Neurology (clinical)

الإتاحة: https://doi.org/10.1093/sleep/27.8.1553Test
http://academic.oup.com/sleep/article-pdf/27/8/1553/13688470/sleep-27-8-1553.pdfTest

المؤلفون: Mancardi, Maria M., Striano, Pasquale, Giannattasio, Alessandro, Baglietto, Maria G., Errichiello, Luca, Zara, Federico, Prato, Giulia, Minuto, Nicola, Veneselli, Edvige, Lorini, Renata, D’Annunzio, Giuseppe

المصدر: Epilepsia ; volume 51, issue 2, page 320-321 ; ISSN 0013-9580 1528-1167

الإتاحة: https://doi.org/10.1111/j.1528-1167.2009.02380.xTest