SCN1A gain of function in early infantile encephalopathy von Berecki, Géza, Bryson, Alexander, Terhag, Jan, Maljevic, Snezana, Gazina, Elena V., Hill, Sean L., Petrou, Steven

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Therapeutic Inhibition of Acid-Sensing Ion Channel 1a Recovers Heart Function After Ischemia–Reperfusion Injury von Redd, Meredith A., Scheuer, Sarah E., Saez, Natalie J., Yoshikawa, Yusuke, Chiu, Han Sheng, Gao, Ling, Hicks, Mark, Villanueva, Jeanette E., Joshi, Yashutosh, Chow, Chun Yuen, Cuellar-Partida, Gabriel, Peart, Jason N., See Hoe, Louise E., Chen, Xiaoli, Sun, Yuliangzi, Suen, Jacky Y., Hatch, Robert J., Rollo, Ben, Xia, Di, Alzubaidi, Mubarak A.H., Maljevic, Snezana, Quaife-Ryan, Gregory A., Hudson, James E., Porrello, Enzo R., White, Melanie Y., Cordwell, Stuart J., Fraser, John F., Petrou, Steven, Reichelt, Melissa E., Thomas, Walter G., King, Glenn F., Macdonald, Peter S., Palpant, Nathan J.

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Developmental dysfunction in a preclinical model of Kcnq2 developmental and epileptic encephalopathy von Mao, Miaomiao, Jancovski, Nikola, Kushner, Yafit, Teasdale, Lucas, Truong, Phan, Zhou, Kun, Reid, Samuel, Jia, Linghan, Aung, Ye Htet, Li, Melody, Reid, Christopher A., Byars, Sean, Scheffer, Ingrid, Petrou, Steven, Maljevic, Snezana

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Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firing von Spyrou, James, Aung, Khaing Phyu, Vanyai, Hannah, Leventer, Richard J., Maljevic, Snezana, Lockhart, Paul J., Howell, Katherine B., Reid, Christopher A.

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Nervous system KV7 disorders: breakdown of a subthreshold brake von Maljevic, Snezana, Wuttke, Thomas V., Lerche, Holger

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Sodium channel expression and transcript variation in the developing brain of human, Rhesus monkey, and mouse von Heighway, Jacqueline, Sedo, Alicia, Garg, Anjali, Eldershaw, Lauren, Perreau, Victoria, Berecki, Géza, Reid, Christopher A., Petrou, Steven, Maljevic, Snezana

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An iPSC line (FINi003-A) from a male with late-onset developmental and epileptic encephalopathy caused by a heterozygous p.E1211K variant in the SCN2A gene encoding the voltage-gat... von Ovchinnikov, Dmitry A., Jong, Sharon, Cuddy, Claire, Dalby, Kelly, Devinsky, Orrin, Mullen, Saul, Maljevic, Snezana, Petrou, Steve

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GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak von Weber, Yvonne G, Storch, Alexander, Wuttke, Thomas V, Brockmann, Knut, Kempfle, Judith, Maljevic, Snezana, Margari, Lucia, Kamm, Christoph, Schneider, Susanne A, Huber, Stephan M, Pekrun, Arnulf, Roebling, Robert, Seebohm, Guiscard, Koka, Saisudha, Lang, Camelia, Kraft, Eduard, Blazevic, Dragica, Salvo-Vargas, Alberto, Fauler, Michael, Mottaghy, Felix M, Münchau, Alexander, Edwards, Mark J, Presicci, Anna, Margari, Francesco, Gasser, Thomas, Lang, Florian, Bhatia, Kailash P, Lehmann-Horn, Frank, Lerche, Holger

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The New Anticonvulsant Retigabine Favors Voltage-Dependent Opening of the Kv7.2 (KCNQ2) Channel by Binding to Its Activation Gate von Wuttke, Thomas V., Seebohm, Guiscard, Bail, Sigrid, Maljevic, Snezana, Lerche, Holger

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SRF modulates seizure occurrence, activity induced gene transcription and hippocampal circuit reorganization in the mouse pilocarpine epilepsy model von Lösing, Pascal, Niturad, Cristina Elena, Harrer, Merle, Reckendorf, Christopher Meyer Zu, Schatz, Theresa, Sinske, Daniela, Lerche, Holger, Maljevic, Snezana, Knöll, Bernd

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Antisense oligonucleotide therapy for KCNT1 encephalopathy von Burbano, Lisseth Estefania, Li, Melody, Jancovski, Nikola, Jafar-Nejad, Paymaan, Richards, Kay, Sedo, Alicia, Soriano, Armand, Rollo, Ben, Jia, Linghan, Gazina, Elena V, Piltz, Sandra, Adikusuma, Fatwa, Thomas, Paul Q, Kopsidas, Helen, Rigo, Frank, Reid, Christopher A, Maljevic, Snezana, Petrou, Steven

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Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies von Krüger, Johanna, Schubert, Julian, Kegele, Josua, Labalme, Audrey, Mao, Miaomiao, Heighway, Jacqueline, Seebohm, Guiscard, Yan, Pu, Koko, Mahmoud, Aslan-Kara, Kezban, Caglayan, Hande, Steinhoff, Bernhard J., Weber, Yvonne G., Keo-Kosal, Pascale, Berkovic, Samuel F., Hildebrand, Michael S., Petrou, Steven, Krause, Roland, May, Patrick, Lesca, Gaetan, Maljevic, Snezana, Lerche, Holger

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Using a Multiplex Nucleic Acid in situ Hybridization Technique to Determine HCN4 mRNA Expression in the Adult Rodent Brain von Oyrer, Julia, Bleakley, Lauren E., Richards, Kay L., Maljevic, Snezana, Phillips, A. Marie, Petrou, Steven, Nowell, Cameron J., Reid, Christopher A.

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Potassium channels: a review of broadening therapeutic possibilities for neurological diseases von Maljevic, Snezana, Lerche, Holger

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Encephalopathies with KCNC1 variants: genotype‐phenotype‐functional correlations von Cameron, Jillian M., Maljevic, Snezana, Nair, Umesh, Aung, Ye Htet, Cogné, Benjamin, Bézieau, Stéphane, Blair, Edward, Isidor, Bertrand, Zweier, Christiane, Reis, André, Koenig, Mary Kay, Maarup, Timothy, Sarco, Dean, Afenjar, Alexandra, Huq, A. H. M. Mahbubul, Kukolich, Mary, Billette de Villemeur, Thierry, Nava, Caroline, Héron, Bénédicte, Petrou, Steven, Berkovic, Samuel F.

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Zebrafish Bioassay-Guided Microfractionation Identifies Anticonvulsant Steroid Glycosides from the Philippine Medicinal Plant Solanum torvum von Challal, Soura, Buenafe, Olivia E. M, Queiroz, Emerson F, Maljevic, Snezana, Marcourt, Laurence, Bock, Merle, Kloeti, Werner, Dayrit, Fabian M, Harvey, Alan L, Lerche, Holger, Esguerra, Camila V, de Witte, Peter A. M, Wolfender, Jean-Luc, Crawford, Alexander D

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CLCN2 variants in idiopathic generalized epilepsy von Kleefuß-Lie, Ailing, Friedl, Waltraut, Cichon, Sven, Haug, Karsten, Warnstedt, Maike, Alekov, Alexi, Sander, Thomas, Ramirez, Alfredo, Poser, Barbara, Maljevic, Snezana, Hebeisen, Simon, Kubisch, Christian, Rebstock, Johannes, Horvath, Steve, Hallmann, Kerstin, Dullinger, Jörn S, Rau, Birgit, Haverkamp, Fritz, Beyenburg, Stefan, Schulz, Herbert, Janz, Dieter, Giese, Bernd, Müller-Newen, Gerhard, Propping, Peter, Elger, Christian E, Fahlke, Christoph, Lerche, Holger

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Molecular analysis of the A322D mutation in the GABAA receptor α1-subunit causing juvenile myoclonic epilepsy von Krampfl, Klaus, Maljevic, Snezana, Cossette, Patrick, Ziegler, Elke, Rouleau, Guy A., Lerche, Holger, Bufler, Johannes

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Models for discovery of targeted therapy in genetic epileptic encephalopathies von Maljevic, Snezana, Reid, Christopher A., Petrou, Steven

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Potassium channel genes and benign familial neonatal epilepsy von Maljevic, Snezana, Lerche, Holger

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