Juvenile Huntington disease in Argentina by Gatto, Emilia Mabel, Parisi, Virginia, Etcheverry, José Luis, Sanguinetti, Ana, Cordi, Lorena, Binelli, Adrian, Persi, Gabriel, Squitieri, Ferdinando

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Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies by 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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4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2 -encephalopathy by Hedrich, Ulrike B S, Lauxmann, Stephan, Wolff, Markus, Synofzik, Matthis, Bast, Thomas, Binelli, Adrian, Serratosa, José M, Martínez-Ulloa, Pedro, Allen, Nicholas M, King, Mary D, Gorman, Kathleen M, Zeev, Bruria Ben, Tzadok, Michal, Wong-Kisiel, Lily, Marjanovic, Dragan, Rubboli, Guido, Sisodiya, Sanjay M, Lutz, Florian, Ashraf, Harshad Pannikkaveettil, Torge, Kirsten, Yan, Pu, Bosselmann, Christian, Schwarz, Niklas, Fudali, Monika, Lerche, Holger

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