Th1 and Th17 but no Th2-related cytokine spectrum in the cerebrospinal fluid of children with Borrelia-related facial nerve palsy

Por Liba, Zuzana, Kayserova, Jana, Komarek, Vladimir
Publicado em 2013

An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome

Por Abdollahpour, Hengameh, Alawi, Malik, Kortüm, Fanny, Beckstette, Michael, Seemanova, Eva, Komárek, Vladimír, Rosenberger, Georg, Kutsche, Kerstin
Publicado no Eur J Hum Genet (2015)

Anti-N-methyl-D-aspartate receptor encephalitis: the clinical course in light of the chemokine and cytokine levels in cerebrospinal fluid

Por Liba, Zuzana, Kayserova, Jana, Elisak, Martin, Marusic, Petr, Nohejlova, Hana, Hanzalova, Jitka, Komarek, Vladimir, Sediva, Anna
Publicado no J Neuroinflammation (2016)

The Sub-Regional Functional Organization of Neocortical Irritative Epileptic Networks in Pediatric Epilepsy

Por Janca, Radek, Krsek, Pavel, Jezdik, Petr, Cmejla, Roman, Tomasek, Martin, Komarek, Vladimir, Marusic, Petr, Jiruska, Premysl
Publicado no Front Neurol (2018)

Corrigendum: The Sub-Regional Functional Organization of Neocortical Irritative Epileptic Networks in Pediatric Epilepsy

Por Janca, Radek, Krsek, Pavel, Jezdik, Petr, Cmejla, Roman, Tomasek, Martin, Komarek, Vladimir, Marusic, Petr, Jiruska, Premysl
Publicado no Front Neurol (2019)

Diffusion Tensor Imaging And Tractography In Autistic, Dysphasic, And Healthy Control Children

Por Hrdlicka, Michal, Sanda, Jan, Urbanek, Tomas, Kudr, Martin, Dudova, Iva, Kickova, Stepanka, Pospisilova, Lenka, Mohaplova, Marketa, Maulisova, Alice, Krsek, Pavel, Kyncl, Martin, Blatny, Marek, Komarek, Vladimir
Publicado no Neuropsychiatr Dis Treat (2019)

Cognitive performance in distinct groups of children undergoing epilepsy surgery—a single-centre experience

Por Benova, Barbora, Belohlavkova, Anezka, Jezdik, Petr, Jahodová, Alena, Kudr, Martin, Komarek, Vladimir, Novak, Vilem, Liby, Petr, Lesko, Robert, Tichý, Michal, Kyncl, Martin, Zamecnik, Josef, Krsek, Pavel, Maulisova, Alice
Publicado no PeerJ (2019)

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Por Suls, Arvid, Jaehn, Johanna A., Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C., Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M., Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S., Giraldez, Beatriz G., Serratosa, José, Lemke, Johannes R., Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S., Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D., Lehesjoki, Anna-Elina, de Witte, Peter A.M., Palotie, Aarno, Lerche, Holger, Esguerra, Camila V., De Jonghe, Peter, Helbig, Ingo
Publicado em 2013