SCN8A self ‐limited infantile epilepsy: Does epilepsy resolve?

Young, Emma ; Harris, Rebekah ; Lieffering, Nico ; de Valles‐Ibáñez, Guillem ; Nyaga, Denis ; Bennett, Mark F. ; Hildebrand, Michael S. ; Scheffer, Ingrid E. ; Sadleir, Lynette G.

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Genotype–phenotype associations in 1018 individuals with SCN1A‐related epilepsies

Gallagher, Declan ; Pérez‐Palma, Eduardo ; Bruenger, Tobias ; Ghanty, Ismael ; Brilstra, Eva ; Ceulemans, Berten ; Chemaly, Nicole ; Lange, Iris ; Depienne, Christel ; Guerrini, Renzo ; Mei, Davide ; Møller, Rikke S. ; Nabbout, Rima ; Regan, Brigid M. ; Schneider, Amy L. ; Scheffer, Ingrid E. ; Schoonjans, An‐Sofie ; Symonds, Joseph D. ; Weckhuysen, Sarah ; Zuberi, Sameer M. ; Lal, Dennis ; Brunklaus, Andreas

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Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing

Coppola, Antonietta ; Krithika, S. ; Iacomino, Michele ; Bobbili, Dheeraj ; Balestrini, Simona ; Bagnasco, Irene ; Bilo, Leonilda ; Buti, Daniela ; Casellato, Susanna ; Cuccurullo, Claudia ; Ferlazzo, Edoardo ; Leu, Costin ; Giordano, Lucio ; Gobbi, Giuseppe ; Hernandez‐Hernandez, Laura ; Lench, Nick ; Martins, Helena ; Meletti, Stefano ; Messana, Tullio ; Nigro, Vincenzo ; Pinelli, Michele ; Pippucci, Tommaso ; Bellampalli, Ravishankara ; Salis, Barbara ; Sofia, Vito ; Striano, Pasquale ; Striano, Salvatore ; Tassi, Laura ; Vignoli, Aglaia ; Vaudano, Anna Elisabetta ; Viri, Maurizio ; Scheffer, Ingrid E. ; May, Patrick ; Zara, Federico ; Sisodiya, Sanjay M.

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Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study

Perry, M. Scott ; Scheffer, Ingrid E. ; Sullivan, Joseph ; Brunklaus, Andreas ; Boronat, Susana ; Wheless, James W. ; Laux, Linda ; Patel, Anup D. ; Roberts, Colin M. ; Dlugos, Dennis ; Holder, Deborah ; Knupp, Kelly G. ; Lallas, Matt ; Phillips, Steven ; Segal, Eric ; Smeyers, Patricia ; Lal, Dennis ; Wirrell, Elaine ; Zuberi, Sameer ; Brünger, Tobias ; Wojnaroski, Mary ; Maru, Benit ; O'Donnell, Penrose ; Morton, Magda ; James, Emma ; Vila, Maria Candida ; Huang, Norman ; Gofshteyn, Jacqueline S. ; Rico, Salvador

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Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial

Sullivan, Joseph ; Lagae, Lieven ; Cross, J Helen ; Devinsky, Orrin ; Guerrini, Renzo ; Knupp, Kelly G ; Laux, Linda ; Nikanorova, Marina ; Polster, Tilman ; Talwar, Dinesh ; Ceulemans, Berten ; Nabbout, Rima ; Farfel, Gail M ; Galer, Bradley S ; Gammaitoni, Arnold R ; Lock, Michael ; Agarwal, Anupam ; Scheffer, Ingrid E

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Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial

Sullivan, Joseph ; Lagae, Lieven ; Cross, J. Helen ; Devinsky, Orrin ; Guerrini, Renzo G ; Knupp, Kelly ; Laux, Linda ; Nikanorova, Marina ; Polster, Tilman ; Talwar, Dinesh ; Ceulemans, Berten ; Nabbout, Rima M ; Farfel, Gail S ; Galer, Bradley R ; Gammaitoni, Arnold ; Lock, Michael ; Agarwal, Anupam E ; Scheffer, Ingrid ; FAiRE, D.S. Study Grp

WILEY

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Indications and prescribing patterns of antiseizure medications in children in New Zealand

Ali, Shayma ; Stanley, James ; Davis, Suzanne ; Keenan, Ngaire ; Scheffer, Ingrid E. ; Sadleir, Lynette G.

England

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Recognition and epileptology of protracted CLN3 disease

Cameron, Jillian M. ; Damiano, John A. ; Grinton, Bronwyn ; Carney, Patrick W. ; McKelvie, Penny ; Silbert, Peter ; Lawn, Nicholas ; Scheffer, Ingrid E. ; Oliver, Karen L. ; Hildebrand, Michael S. ; Berkovic, Samuel F.

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Differential diagnosis of familial adult myoclonic epilepsy

Baykan, Betul ; Franceschetti, Silvana ; Canafoglia, Laura ; Cavalleri, Gianpiero L. ; Michelucci, Roberto ; Scheffer, Ingrid E.

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Genes4Epilepsy: An epilepsy gene resource

Oliver, Karen L. ; Scheffer, Ingrid E. ; Bennett, Mark F. ; Grinton, Bronwyn E. ; Bahlo, Melanie ; Berkovic, Samuel F.

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