Browsing by Author Sadleir, Lynette

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Showing results 1 to 4 of 4
Issue DateTitleAuthor(s)Citation
2016Exome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsyBagnall, Richard; Cutmore, Carina; Duflou, Johan; Lam, Lien; Semsarian, Chris; Cairns, Anita; Crompton, Douglas; Dibbens, Leanne; et al, Various; Garry, Sarah I; Kivity, Sara; Petrovski, Slave; Sadleir, Lynette; Central Clinical School: Medicine; Science Faculty Admin; Central Clinical School: Medicine; Central Clinical School: Office; Central Clinical School: Centenary InstituteExome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsy, Annals of Neurology, vol.79, 4, 2016,pp 522-534
2017Not all SCN1A epileptic encephalopathies are Dravet syndromeGill, Deepak; Davis, Suzanne; DeVile, Catherine; et al, Various; Joshi, Charuta; Kurian, Manju; Mandalstem, Simone; Mountier, Emily; Murali, Hema; Nickels, Katherine; Sadleir, Lynette; Wirrell, Elaine; Westmead Clinical School: MedicineNot all SCN1A epileptic encephalopathies are Dravet syndrome, Neurology, vol.89, 10, 2017,pp 1035-1042
2013Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndromeBleasel, Andrew; Andermann, Eva; Bellows, Susannah; et al, Various; Farrell, K.; Gill, Deepak S; Harbord, M; Hodgson, Bree; Iona, Xenia; Mackay, Mark; McMahon, Jacinta; Mullen, Saul A; Mulley, John C; Sadleir, Lynette; Sisodiya, Sanyjay; Webster, Richard; Wirrel, Elaine; Deans Unit: (CIPHER)Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome, Epilepsia, vol.54, 9, 2013,pp e122-e126
2013Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Bleasel, Andrew; Afawi, Zaid; Andrade, Danielle M; Berkovic, Samuel F.; Bye, Ann M. E.; Calvert, Sophie; Carvill, Gemma L; Cook, Joseph; Dorschner, Michael O; Freeman, Jeremy L; Gill, D S; Heavin, Sinead; Howell, Katherine B; Khan, Adiba; Kivity, Sara; Korczyn, Amos; Lerman-Sagie, Tally; Lev, Dorit; Møller2, Rikke S; Mackay, Mark; Malone, Stephen; McMahon, Jacinta; Mefford, Heather; O’Roak, Brian J; Rodriguez-Casero, Victoria; Sadleir, Lynette; Scheffer, Ingrid; Shendure, Jay; Stanley, Thorsten; Wallace, Geoffrey; Weaver, Molly; Webster, Richard; Yendle, Simone; Zelnick, Nathanel; Deans Unit: (CIPHER)Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1, Nature Genetics, vol.45, 7, 2013,pp 825-830