Phenotypic and genetic spectrum of SCN8A‐related disorders, treatment options, and outcomes von Gardella, Elena, Møller, Rikke S.

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Diagnostic accuracy of the Salzburg EEG criteria for non-convulsive status epilepticus: a retrospective study von Leitinger, Markus, MD, Trinka, Eugen, Prof, Gardella, Elena, MD, Rohracher, Alexandra, MD, Kalss, Gudrun, MD, Qerama, Erisela, MD, Höfler, Julia, MD, Hess, Alexander, MD, Zimmermann, Georg, MSc, Kuchukhidze, Giorgi, MD, Dobesberger, Judith, MD, Langthaler, Patrick B, BSc, Beniczky, Sándor, Dr

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Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies von Masnada, Silvia, Hedrich, Ulrike B S, Gardella, Elena, Schubert, Julian, Kaiwar, Charu, Klee, Eric W, Lanpher, Brendan C, Gavrilova, Ralitza H, Synofzik, Matthis, Bast, Thomas, Gorman, Kathleen, King, Mary D, Allen, Nicholas M, Conroy, Judith, Ben Zeev, Bruria, Tzadok, Michal, Korff, Christian, Dubois, Fanny, Ramsey, Keri, Narayanan, Vinodh, Serratosa, Jose M, Giraldez, Beatriz G, Helbig, Ingo, Marsh, Eric, O'Brien, Margaret, Bergqvist, Christina A, Binelli, Adrian, Porter, Brenda, Zaeyen, Eduardo, Horovitz, Dafne D, Wolff, Markus, Marjanovic, Dragan, Caglayan, Hande S, Arslan, Mutluay, Pena, Sergio D J, Sisodiya, Sanjay M, Balestrini, Simona, Syrbe, Steffen, Veggiotti, Pierangelo, Lemke, Johannes R, Møller, Rikke S, Lerche, Holger, Rubboli, Guido

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Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation von Gardella, Elena, Becker, Felicitas, Møller, Rikke S., Schubert, Julian, Lemke, Johannes R., Larsen, Line H. G., Eiberg, Hans, Nothnagel, Michael, Thiele, Holger, Altmüller, Janine, Syrbe, Steffen, Merkenschlager, Andreas, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Mang, Yuan, Bakke Møller, Louise, Gellert, Pia, Heron, Sarah E., Dibbens, Leanne M., Weckhuysen, Sarah, Dahl, Hans Atli, Biskup, Saskia, Tommerup, Niels, Hjalgrim, Helle, Lerche, Holger, Beniczky, Sándor, Weber, Yvonne G.

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Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies von Absalom, Nathan L., Liao, Vivian W. Y., Johannesen, Katrine M. H., Gardella, Elena, Jacobs, Julia, Lesca, Gaetan, Gokce-Samar, Zeynep, Arzimanoglou, Alexis, Zeidler, Shimriet, Striano, Pasquale, Meyer, Pierre, Benkel-Herrenbrueck, Ira, Mero, Inger-Lise, Rummel, Jutta, Chebib, Mary, Møller, Rikke S., Ahring, Philip K.

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Standardized computer-based organized reporting of EEG: SCORE – Second version von Beniczky, Sándor, Aurlien, Harald, Brøgger, Jan C., Hirsch, Lawrence J., Schomer, Donald L., Trinka, Eugen, Pressler, Ronit M., Wennberg, Richard, Visser, Gerhard H., Eisermann, Monika, Diehl, Beate, Lesser, Ronald P., Kaplan, Peter W., Nguyen The Tich, Sylvie, Lee, Jong Woo, Martins-da-Silva, Antonio, Stefan, Hermann, Neufeld, Miri, Rubboli, Guido, Fabricius, Martin, Gardella, Elena, Terney, Daniella, Meritam, Pirgit, Eichele, Tom, Asano, Eishi, Cox, Fieke, van Emde Boas, Walter, Mameniskiene, Ruta, Marusic, Petr, Zárubová, Jana, Schmitt, Friedhelm C., Rosén, Ingmar, Fuglsang-Frederiksen, Anders, Ikeda, Akio, MacDonald, David B., Terada, Kiyohito, Ugawa, Yoshikazu, Zhou, Dong, Herman, Susan T.

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Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function von Zilmer, Monica, Edmondson, Andrew C, Khetarpal, Sumeet A, Alesi, Viola, Zaki, Maha S, Rostasy, Kevin, Madsen, Camilla G, Lepri, Francesca R, Sinibaldi, Lorenzo, Cusmai, Raffaella, Novelli, Antonio, Issa, Mahmoud Y, Fenger, Christina D, Abou Jamra, Rami, Reutter, Heiko, Briuglia, Silvana, Agolini, Emanuele, Hansen, Lars, Petäjä-Repo, Ulla E, Hintze, John, Raymond, Kimiyo M, Liedtke, Kristen, Stanley, Valentina, Musaev, Damir, Gleeson, Joseph G, Vitali, Cecilia, O'Brien, W Timothy, Gardella, Elena, Rubboli, Guido, Rader, Daniel J, Schjoldager, Katrine T, Møller, Rikke S

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Mutations in KCNT1 cause a spectrum of focal epilepsies von Møller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., 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.

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Sex-specific disease modifiers in juvenile myoclonic epilepsy von Shakeshaft, Amy, Panjwani, Naim, Collingwood, Amber, Crudgington, Holly, Hall, Anna, Andrade, Danielle M., Beier, Christoph P., Fong, Choong Yi, Gardella, Elena, Gesche, Joanna, Greenberg, David A., Hamandi, Khalid, Koht, Jeanette, Lim, Kheng Seang, Møller, Rikke S., Ng, Ching Ching, Orsini, Alessandro, Rees, Mark I., Rubboli, Guido, Selmer, Kaja K., Striano, Pasquale, Syvertsen, Marte, Thomas, Rhys H., Zarubova, Jana, Richardson, Mark P., Strug, Lisa J., Pal, Deb K.

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PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics von Bayat, Allan, Knaus, Alexej, Juul, Annika Wollenberg, Dukic, Dejan, Gardella, Elena, Charzewska, Agnieszka, Clement, Emma, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Horn, Denise, Horton, Rachel, Hurst, Jane A., Josifova, Dragana, Larsen, Line H. G., Lascelles, Karine, Obersztyn, Ewa, Pagnamenta, Alistair, Pal, Deb K., Pendziwiat, Manuela, Ryten, Mina, Taylor, Jenny, Vogt, Julie, Weber, Yvonne, Krawitz, Peter M., Helbig, Ingo, Kini, Usha, Møller, Rikke S.

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STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEG von Houtman, Simon J, Lammertse, Hanna C A, van Berkel, Annemiek A, Balagura, Ganna, Gardella, Elena, Ramautar, Jennifer R, Reale, Chiara, Møller, Rikke S, Zara, Federico, Striano, Pasquale, Misra-Isrie, Mala, van Haelst, Mieke M, Engelen, Marc, van Zuijen, Titia L, Mansvelder, Huibert D, Verhage, Matthijs, Bruining, Hilgo, Linkenkaer-Hansen, Klaus

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EEG normal variants: A prospective study using the SCORE system von Wüstenhagen, Stephan, Terney, Daniella, Gardella, Elena, Meritam Larsen, Pirgit, Rømer, Connie, Aurlien, Harald, Beniczky, Sándor

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A wavelet-based energetic approach for the analysis of biomedical signals: Application to the electroencephalogram and electro-oculogram von Magosso, Elisa, Ursino, Mauro, Zaniboni, Anna, Gardella, Elena

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Mild malformations of cortical development in sleep‐related hypermotor epilepsy due to KCNT1 mutations von Rubboli, Guido, Plazzi, Giuseppe, Picard, Fabienne, Nobili, Lino, Hirsch, Edouard, Chelly, Jamel, Prayson, Richard A., Boutonnat, Jean, Bramerio, Manuela, Kahane, Philippe, Dibbens, Leanne M., Gardella, Elena, Baulac, Stéphanie, Møller, Rikke S.

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Sleep disturbances in SCN8A‐related disorders von Furia, Francesca, Johannesen, Katrine M., Bonardi, Claudia M., Previtali, Roberto, Aledo‐Serrano, Angel, Mastrangelo, Massimo, Favaro, Jacopo, Masnada, Silvia, Micco, Valentina, Proietti, Jacopo, Veggiotti, Pierangelo, Rubboli, Guido, Cantalupo, Gaetano, Olofsson, Kern, Møller, Rikke S., Gardella, Elena

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Reader response: Generalized polyspike train: An EEG biomarker of drug-resistant idiopathic generalized epilepsy von Rubboli, Guido, Gardella, Elena

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Effect of fenfluramine on seizures and comorbidities in SCN8A‐developmental and epileptic encephalopathy: A case series von Aledo‐Serrano, Ángel, Cabal‐Paz, Borja, Gardella, Elena, Gómez‐Porro, Pablo, Martínez‐Múgica, Otilia, Beltrán‐Corbellini, Alvaro, Toledano, Rafael, García‐Morales, Irene, Gil‐Nagel, Antonio

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Vinpocetine improved neuropsychiatric and epileptic outcomes in a patient with a GABRA1 loss‐of‐function variant von Gjerulfsen, Cathrine E., Mieszczanek, Tomasz S., Johannesen, Katrine M., Liao, Vivian W. Y., Chebib, Mary, Nørby, Helene A. J., Gardella, Elena, Rubboli, Guido, Ahring, Philip, Møller, Rikke S.

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Phenotypic and genetic spectrum of SCN 8A ‐related disorders, treatment options, and outcomes von Gardella, Elena, Møller, Rikke S.

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Epilepsy in neurodegenerative diseases von Neri, Sabrina, Mastroianni, Giovanni, Gardella, Elena, Aguglia, Umberto, Rubboli, Guido

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