Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Seizures and KCNA2[original query] |
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Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. Molecular syndromology 2016 Sep 7 (4): 210-219. Møller Rikke S, Larsen Line H G, Johannesen Katrine M, Talvik Inga, Talvik Tiina, Vaher Ulvi, Miranda Maria J, Farooq Muhammad, Nielsen Jens E K, Svendsen Lene Lavard, Kjelgaard Ditte B, Linnet Karen M, Hao Qin, Uldall Peter, Frangu Mimoza, Tommerup Niels, Baig Shahid M, Abdullah Uzma, Born Alfred P, Gellert Pia, Nikanorova Marina, Olofsson Kern, Jepsen Birgit, Marjanovic Dragan, Al-Zehhawi Lana I K, Peñalva Sofia J, Krag-Olsen Bente, Brusgaard Klaus, Hjalgrim Helle, Rubboli Guido, Pal Deb K, Dahl Hans |
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies. Brain : a journal of neurology 2017 10 140 (9): 2337-2354. 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 Gui |
Tiered analysis of whole-exome sequencing for epilepsy diagnosis. Molecular genetics and genomics : MGG 2020 3 295 (3): 751-763. Dunn Paul J, Maher Bridget H, Albury Cassie L, Stuart Shani, Sutherland Heidi G, Maksemous Neven, Benton Miles C, Smith Robert A, Haupt Larisa M, Griffiths Lyn |
Unusual Voltage-Gated Sodium and Potassium Channelopathies Related to Epilepsy. Journal of clinical neurology (Seoul, Korea) 2024 7 20 (4): 402-411. Hui Jin Shin, Ara Ko, Se Hee Kim, Joon Soo Lee, Hoon-Chul Ka |
Next-generation sequencing testing in children with epilepsy reveals novel clinical, diagnostic and therapeutic implications. Frontiers in genetics 2024 1 14 1300952. Magdalena Krygier, Marta Pietruszka, Marta Zawadzka, Agnieszka Sawicka, Anna Lemska, Monika Limanówka, Jan ?urek, Weronika Tala?ka-Liczbik, Maria Mazurkiewicz-Be?dzi?s |
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