SCN1A‐related phenotypes: Epilepsy and beyond von Scheffer, Ingrid E., Nabbout, Rima

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The genetic landscape of the epileptic encephalopathies of infancy and childhood von McTague, Amy, MBChB, Howell, Katherine B, MBBS, Cross, J Helen, Prof, Kurian, Manju A, PhD, Scheffer, Ingrid E, Prof

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Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome von Devinsky, Orrin, Cross, J. Helen, Laux, Linda, Marsh, Eric, Miller, Ian, Nabbout, Rima, Scheffer, Ingrid E, Thiele, Elizabeth A, Wright, Stephen

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The new definition and classification of seizures and epilepsy von Falco-Walter, Jessica J., Scheffer, Ingrid E., Fisher, Robert S.

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Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology von Fisher, Robert S., Cross, J. Helen, French, Jacqueline A., Higurashi, Norimichi, Hirsch, Edouard, Jansen, Floor E., Lagae, Lieven, Moshé, Solomon L., Peltola, Jukka, Roulet Perez, Eliane, Scheffer, Ingrid E., Zuberi, Sameer M.

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ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology von Scheffer, Ingrid E., Berkovic, Samuel, Capovilla, Giuseppe, Connolly, Mary B., French, Jacqueline, Guilhoto, Laura, Hirsch, Edouard, Jain, Satish, Mathern, Gary W., Moshé, Solomon L., Nordli, Douglas R., Perucca, Emilio, Tomson, Torbjörn, Wiebe, Samuel, Zhang, Yue‐Hua, Zuberi, Sameer M.

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International consensus on diagnosis and management of Dravet syndrome von Wirrell, Elaine C., Hood, Veronica, Knupp, Kelly G., Meskis, Mary Anne, Nabbout, Rima, Scheffer, Ingrid E., Wilmshurst, Jo, Sullivan, Joseph

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Genetic architecture of childhood speech disorder: a review von Morgan, Angela T., Amor, David J., St John, Miya D., Scheffer, Ingrid. E., Hildebrand, Michael S.

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Instruction manual for the ILAE 2017 operational classification of seizure types von Fisher, Robert S., Cross, J. Helen, D'Souza, Carol, French, Jacqueline A., Haut, Sheryl R., Higurashi, Norimichi, Hirsch, Edouard, Jansen, Floor E., Lagae, Lieven, Moshé, Solomon L., Peltola, Jukka, Roulet Perez, Eliane, Scheffer, Ingrid E., Schulze‐Bonhage, Andreas, Somerville, Ernest, Sperling, Michael, Yacubian, Elza Márcia, Zuberi, Sameer M.

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ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions von Hirsch, Edouard, French, Jacqueline, Scheffer, Ingrid E., Bogacz, Alicia, Alsaadi, Taoufik, Sperling, Michael R., Abdulla, Fatema, Zuberi, Sameer M., Trinka, Eugen, Specchio, Nicola, Somerville, Ernest, Samia, Pauline, Riney, Kate, Nabbout, Rima, Jain, Satish, Wilmshurst, Jo M., Auvin, Stephane, Wiebe, Samuel, Perucca, Emilio, Moshé, Solomon L., Tinuper, Paolo, Wirrell, Elaine C., Adikaibe, Drs Birinus, Al Baradi, Raidah, Andrade, Danielle, Bast, Thomas, Beydoun, Ahmed, Bien, Christian, Caraballo, Roberto, Carolina Coan, Ana, Connolly, Mary, Dunne, John, Haut, Sheryl, Jansen, Floor, Jobst, Barbara, Kalviainen, Reetta, Kakooza, Angela, Kato, Mitsuhiro, Knupp, Kelly, Kochen, Silvia, Lagae, Lieven, Carlos Mayor, Luis, Okujava, Natela, Radakishnan, Kurupath, Roulet‐Perez, Eliane, Rios, Loreto, Sadleir, Lynette, Juan‐Orta, Daniel San, Serratosa, Jose, Shellhaas, Renee, Tsai, Meng‐Han, Udani, Vrajesh, Yue‐Hua Zhang, Helen, Zhou, Dong

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New concepts in classification of the epilepsies: Entering the 21st century von Berg, Anne T., Scheffer, Ingrid E.

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ILAE Official Report: A practical clinical definition of epilepsy von Fisher, Robert S., Acevedo, Carlos, Arzimanoglou, Alexis, Bogacz, Alicia, Cross, J. Helen, Elger, Christian E., Engel, Jerome, Forsgren, Lars, French, Jacqueline A., Glynn, Mike, Hesdorffer, Dale C., Lee, B.I., Mathern, Gary W., Moshé, Solomon L., Perucca, Emilio, Scheffer, Ingrid E., Tomson, Torbjörn, Watanabe, Masako, Wiebe, Samuel

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A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity von Kolc, Kristy L, Sadleir, Lynette G, Scheffer, Ingrid E, Ivancevic, Atma, Roberts, Rachel, Pham, Duyen H, Gecz, Jozef

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Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk von Myers, Kenneth A., Bello‐Espinosa, Luis E., Symonds, Joseph D., Zuberi, Sameer M., Clegg, Robin, Sadleir, Lynette G., Buchhalter, Jeffrey, Scheffer, Ingrid E.

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Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy von Bagnall, Richard D., Crompton, Douglas E., Petrovski, Slavé, Lam, Lien, Cutmore, Carina, Garry, Sarah I., Sadleir, Lynette G., Dibbens, Leanne M., Cairns, Anita, Kivity, Sara, Afawi, Zaid, Regan, Brigid M., Duflou, Johan, Berkovic, Samuel F., Scheffer, Ingrid E., Semsarian, Christopher

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Early and effective treatment of KCNQ2 encephalopathy von Pisano, Tiziana, Numis, Adam L., Heavin, Sinéad B., Weckhuysen, Sarah, Angriman, Marco, Suls, Arvid, Podesta, Barbara, Thibert, Ronald L., Shapiro, Kevin A., Guerrini, Renzo, Scheffer, Ingrid E., Marini, Carla, Cilio, Maria Roberta

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Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009 von Berg, Anne T., Berkovic, Samuel F., Brodie, Martin J., Buchhalter, Jeffrey, Cross, J. Helen, Van Emde Boas, Walter, Engel, Jerome, French, Jacqueline, Glauser, Tracy A., Mathern, Gary W., Moshé, Solomon L., Nordli, Douglas, Plouin, Perrine, Scheffer, Ingrid E.

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A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development von Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T., Shriberg, Lawrence D., Fisher, Simon E.

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The genetics of Dravet syndrome von Marini, Carla, Scheffer, Ingrid E., Nabbout, Rima, Suls, Arvid, De Jonghe, Peter, Zara, Federico, Guerrini, Renzo

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Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy von Ricos, Michael G., Hodgson, Bree L., Pippucci, Tommaso, Saidin, Akzam, Ong, Yeh Sze, Heron, Sarah E., Licchetta, Laura, Bisulli, Francesca, Bayly, Marta A., Hughes, James, Baldassari, Sara, Palombo, Flavia, Santucci, Margherita, Meletti, Stefano, Berkovic, Samuel F., Rubboli, Guido, Thomas, Paul Q., Scheffer, Ingrid E., Tinuper, Paolo, Geoghegan, Joel, Schreiber, Andreas W., Dibbens, Leanne M.

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