Treatment of MOG antibody associated disorders: results of an international survey von Whittam, D. H., Karthikeayan, V., Gibbons, E., Kneen, R., Chandratre, S., Ciccarelli, O., Hacohen, Y., de Seze, J., Deiva, K., Hintzen, R. Q., Wildemann, B., Jarius, S., Kleiter, I., Rostasy, K., Huppke, P., Hemmer, B., Paul, F., Aktas, O., Pröbstel, A. K., Arrambide, G., Tintore, M., Amato, M. P., Nosadini, M., Mancardi, M. M., Capobianco, M., Illes, Z., Siva, A., Altintas, A., Akman-Demir, G., Pandit, L., Apiwattankul, M., Hor, J. Y., Viswanathan, S., Qiu, W., Kim, H. J., Nakashima, I., Fujihara, K., Ramanathan, S., Dale, R. C., Boggild, M., Broadley, S., Lana-Peixoto, M. A., Sato, D. K., Tenembaum, S., Cabre, P., Wingerchuk, D. M., Weinshenker, B. G., Greenberg, B., Matiello, M., Klawiter, E. C., Bennett, J. L., Wallach, A. I., Kister, I., Banwell, B. L., Traboulsee, A., Pohl, D., Palace, J., Leite, M. I., Levy, M., Marignier, R., Solomon, T., Lim, M., Huda, S., Jacob, A.

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Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya Vasculopathy von Tortora, D, Severino, M, Pacetti, M, Morana, G, Mancardi, M M, Capra, V, Cama, A, Pavanello, M, Rossi, A

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An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy von STRIANO, P, COPPOLA, A, RASMINI, P, BESANA, D, COPPOLA, G. G, ELIA, M, GRANATA, T, VECCHI, M, VIGEVANO, F, VIRI, M, GAGGERO, R, STRIANO, S, PEZZELLA, M, ZARA, F, CIAMPA, C, SPECCHIO, N, RAGONA, F, MANCARDI, M. M, GENNARO, E, BECCARIA, F, CAPOVILLA, G

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17q23.3 de novo microdeletion involving only TANC2 gene: A new case von Tassano, E., Accogli, A., Ronchetto, P., Tortora, D., Tavella, E., Gimelli, G., Mancardi, M., Malacarne, M., Coviello, D.A.

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Substrate reduction therapy with Miglustat in pediatric patients with GM1 type 2 gangliosidosis delays neurological involvement: A multicenter experience von Fischetto, Rita, Palladino, Valentina, Mancardi, Maria M., Giacomini, Thea, Palladino, Stefano, Gaeta, Alberto, Di Rocco, Maja, Zampini, Lucia, Lassandro, Giuseppe, Favia, Vito, Tripaldi, Maria E., Strisciuglio, Pietro, Romano, Alfonso, Severino, Mariasavina, Morrone, Amelia, Giordano, Paola

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Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathy von Mirabelli-Badenier, M, Biancheri, R, Morana, G, Fornarino, S, Siri, L, Celle, M.E, Veneselli, E, Vincent, A, Gaggero, R, Mancardi, M.M

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Gluten psychosis: A case report and review of literature von Lionetti, E, Leonardi, S, Franzonello, C, Mancardi, M, Ruggieri, M, Catassi, C

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Novel CNS malformations and skeletal anomalies in a patient with Beaulieu‐boycott‐Innes syndrome von Accogli, Andrea, Scala, Marcello, Calcagno, Annalisa, Castello, Raffaele, Torella, Annalaura, Musacchia, Francesco, Allegri, Anna M. E., Mancardi, Maria M., Maghnie, Mohamad, Severino, Mariasavina, Nigro, Vincenzo, Capra, Valeria

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Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism von Fornarino, Stefania, Stagnaro, Michela, Rinelli, Martina, Tiziano, Danilo, Mancardi, Margherita M, Traverso, Maria, Veneselli, Edvige, De Grandis, Elisa

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Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants von Malerba, Federica, Alberini, Giulio, Balagura, Ganna, Marchese, Francesca, Amadori, Elisabetta, Riva, Antonella, Vari, Maria Stella, Gennaro, Elena, Madia, Francesca, Salpietro, Vincenzo, Angriman, Marco, Giordano, Lucio, Accorsi, Patrizia, Trivisano, Marina, Specchio, Nicola, Russo, Angelo, Gobbi, Giuseppe, Raviglione, Federico, Pisano, Tiziana, Marini, Carla, Mancardi, Maria M., Nobili, Lino, Freri, Elena, Castellotti, Barbara, Capovilla, Giuseppe, Coppola, Antonietta, Verrotti, Alberto, Martelli, Paola, Miceli, Francesco, Maragliano, Luca, Benfenati, Fabio, Cilio, Maria R., Johannesen, Kathrine M., Møller, Rikke S., Ceulemans, Berten, Minetti, Carlo, Weckhuysen, Sarah, Zara, Federico, Taglialatela, Maurizio, Striano, Pasquale

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Hashimoto's Encephalopathy with Selective Involvement of the Nucleus Accumbens: A Case Report von Mancardi, M. M., Fazzini, F., Rossi, A., Gaggero, R.

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Sleep disorders and neuropsychiatric disorders in a pediatric sample of tuberous sclerosis complex: a questionnaire-based study von Moavero, R., Voci, A., La Briola, F., Matricardi, S., Toldo, I., Mancardi, M., Negrin, S., Vigevano, F., Mazzone, L., Valeriani, M., Curatolo, P., Bruni, O.

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Type 1 diabetes and epilepsy: More than a casual association? von 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

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KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum von Bonardi, Claudia M, Heyne, Henrike O, Fiannacca, Martina, Fitzgerald, Mark P, Gardella, Elena, Gunning, Boudewijn, Olofsson, Kern, Lesca, Gaétan, Verbeek, Nienke, Stamberger, Hannah, Striano, Pasquale, Zara, Federico, Mancardi, Maria M, Nava, Caroline, Syrbe, Steffen, Buono, Salvatore, Baulac, Stephanie, Coppola, Antonietta, Weckhuysen, Sarah, Schoonjans, An-Sofie, Ceulemans, Berten, Sarret, Catherine, Baumgartner, Tobias, Muhle, Hiltrud, Portes, Vincent des, Toulouse, Joseph, Nougues, Marie-Christine, Rossi, Massimiliano, Demarquay, Geneviève, Ville, Dorothée, Hirsch, Edouard, Maurey, Hélène, Willems, Marjolaine, de Bellescize, Julitta, Altuzarra, Cecilia Desmettre, Villeneuve, Nathalie, Bartolomei, Fabrice, Picard, Fabienne, Hornemann, Frauke, Koolen, David A, Kroes, Hester Y, Reale, Chiara, Fenger, Christina D, Tan, Wen-Hann, Dibbens, Leanne, Bearden, David R, Møller, Rikke S, Rubboli, Guido

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Autologous haematopoietic stem-cell transplantation in multiple sclerosis von Mancardi, Gianluigi, MD, Saccardi, Riccardo, MD

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TBC1D24 genotype–phenotype correlation: Epilepsies and other neurologic features von Balestrini, Simona, Milh, Mathieu, Castiglioni, Claudia, Lüthy, Kevin, Finelli, Mattea J, Verstreken, Patrik, Cardon, Aaron, Stražišar, Barbara Gnidovec, Holder, J Lloyd, Lesca, Gaetan, Mancardi, Maria M, Poulat, Anne L, Repetto, Gabriela M, Banka, Siddharth, Bilo, Leonilda, Birkeland, Laura E, Bosch, Friedrich, Brockmann, Knut, Cross, J Helen, Doummar, Diane, Félix, Temis M, Giuliano, Fabienne, Hori, Mutsuki, Hüning, Irina, Kayserili, Hulia, Kini, Usha, Lees, Melissa M, Meenakshi, Girish, Mewasingh, Leena, Pagnamenta, Alistair T, Peluso, Silvio, Mey, Antje, Rice, Gregory M, Rosenfeld, Jill A, Taylor, Jenny C, Troester, Matthew M, Stanley, Christine M, Ville, Dorothee, Walkiewicz, Magdalena, Falace, Antonio, Fassio, Anna, Lemke, Johannes R, Biskup, Saskia, Tardif, Jessica, Ajeawung, Norbert F, Tolun, Aslihan, Corbett, Mark, Gecz, Jozef, Afawi, Zaid, Howell, Katherine B, Oliver, Karen L, Berkovic, Samuel F, Scheffer, Ingrid E, de Falco, Fabrizio A, Oliver, Peter L, Striano, Pasquale, Zara, Federico, Campeau, Phillipe M, Sisodiya, S.M

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IAP042 Opsoclonus-Myoclonus-Ataxia: neuropsychological and neuroradiological sequelae von De Grandis, E, Battaglia, F, Pessagno, A, Liberati, P, Angelini, P, Conte, M, Gandolfo, C, Morana, G, Mancardi, M, Veneselli, E

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Ultra-rare genetic variation in the epilepsies: A whole-exome sequencing study of 17,606 individuals von Feng, Y-CA, Howrigan, DP, Tashman, K, Cerrato, F, Churchhouse, C, Dhindsa, RS, Stanley, KE, Weckhuysen, S, Sisodiya, SM, Cotsapas, C, De Jonghe, P, Kwan, P, Marson, AG, Stewart, R, Dlugos, DJ, Scheffer, IE, Striano, P, Freyer, C, Bellows, ST, Leu, C, Macdonald, A, Burgess, R, Weckhuysen, D, Bahlo, M, Papacostas, SS, Laššuthová, P, Reif, PS, Kunz, WS, Zsurka, G, Elger, CE, Bauer, J, Rademacher, M, Pendziwiat, M, Rademacher, A, Kluger, G, Häusler, M, Becker, F, Rau, S, Steinhoff, BJ, Schubert-Bast, S, Borggräfe, I, Madeleyn, R, Saarela, A, Linnankivi, T, Rees, MI, Chung, S-K, Powell, R, Schneider, N, Braatz, V, Auce, P, Sham, PC, Delanty, N, McCormack, M, Canafoglia, L, Castellotti, B, Iacomino, M, Mancardi, MM, Tinuper, P, Licchetta, L, Stipa, C, Manna, L, Gagliardi, M, Parrini, E, Vetro, A, Bianchini, C, Doccini, V, Yamakawa, K, King, C, Arslan, M, Yapıcı, Z, Yis, U, Topaloglu, P, Uğur-İşeri, S, Baykan, B, Salman, B, Kesim, Y, Özkara, Ç, Shiedley, BR, Buono, RJ, Ferraro, TN, Privitera, M, Kuzniecky, RI, Hegde, M, Ellis, CA, Ciullo, V, Reif, A, McQuillin, A, McIntosh, A, Blackwood, D, Carvalho, CB, Malaspina, D, Morley, CP, Perkins, DO, Knowles, JA, McCarroll, SA, Gupta, N, Lander, ES, Goldstein, DB, Lerche, H, Neale, BM

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TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features von Balestrini, Simona, Milh, Mathieu, Castiglioni, Claudia, Lüthy, Kevin, Finelli, Mattea J, Verstreken, Patrik, Cardon, Aaron, Stražišar, Barbara Gnidovec, Holder, J. Lloyd, Lesca, Gaetan, Mancardi, Maria M, Poulat, Anne L, Repetto, Gabriela M, Banka, Siddharth, Bilo, Leonilda, Birkeland, Laura E, Bosch, Friedrich, Brockmann, Knut, Cross, J. Helen, Doummar, Diane, Félix, Temis M, Giuliano, Fabienne, Hori, Mutsuki, Hüning, Irina, Kayserili, Hulia, Kini, Usha, Lees, Melissa M, Meenakshi, Girish, Mewasingh, Leena, Pagnamenta, Alistair T, Peluso, Silvio, Mey, Antje, Rice, Gregory M, Rosenfeld, Jill A, Taylor, Jenny C, Troester, Matthew M, Stanley, Christine M, Ville, Dorothee, Walkiewicz, Magdalena, Falace, Antonio, Fassio, Anna, Lemke, Johannes R, Biskup, Saskia, Tardif, Jessica, Ajeawung, Norbert F, Tolun, Aslihan, Corbett, Mark, Gecz, Jozef, Afawi, Zaid, Howell, Katherine B, Oliver, Karen L, Berkovic, Samuel F, Scheffer, Ingrid E, de Falco, Fabrizio A, Oliver, Peter L, Striano, Pasquale, Zara, Federico, Campeau, Phillipe M, Sisodiya, S.M

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Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

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