Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Robyn, Fahlstrom"'
Autor:
Peter, Widdess-Walsh, Dennis, Dlugos, Robyn, Fahlstrom, Sucheta, Joshi, Renée, Shellhaas, Alex, Boro, Joseph, Sullivan, Eric, Geller, Melodie, Winawer
Publikováno v:
Epilepsia. 54:1898-1904
Summary Purpose Lennox-Gastaut syndrome (LGS) is a devastating childhood-onset epilepsy syndrome. The cause is unknown in 25% of cases. Little has been described about the specific clinical or electroencephalography (EEG) features of LGS of unknown o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6160fa784ca73d687e96e55475878fed
https://doi.org/10.1111/epi.12395
https://doi.org/10.1111/epi.12395
Publikováno v:
Neurology. 89(1)
Objective:To improve phenotype definition in genetic studies of epilepsy, we assessed the familial aggregation of focal seizure types and of specific seizure symptoms within the focal epilepsies in families from the Epilepsy Phenome/Genome Project.Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca1f640c40d59dfa4fe0d69a56a4796
https://pubmed.ncbi.nlm.nih.gov/28566546
https://pubmed.ncbi.nlm.nih.gov/28566546
Autor:
Bassel, Abou-Khalil, Brian, Alldredge, Jocelyn, Bautista, Sam, Berkovic, Judith, Bluvstein, Alex, Boro, Gregory, Cascino, Damian, Consalvo, Sabrina, Cristofaro, Patricia, Crumrine, Orrin, Devinsky, Dennis, Dlugos, Michael, Epstein, Robyn, Fahlstrom, Miguel, Fiol, Nathan, Fountain, Kristen, Fox, Jacqueline, French, Catharine, Freyer Karn, Daniel, Friedman, Eric, Geller, Tracy, Glauser, Simon, Glynn, Kevin, Haas, Sheryl, Haut, Jean, Hayward, Sandra, Helmers, Sucheta, Joshi, Andres, Kanner, Heidi, Kirsch, Robert, Knowlton, Eric, Kossoff, Rachel, Kuperman, Ruben, Kuzniecky, Daniel, Lowenstein, Shannon, McGuire, Paul, Motika, Gerard, Nesbitt, Edward, Novotny, Ruth, Ottman, Juliann, Paolicchi, Jack, Parent, Kristen, Park, Annapurna, Poduri, Neil, Risch, Lynette, Sadleir, Ingrid, Scheffer, Renee, Shellhaas, Elliott, Sherr, Jerry J, Shih, Shlomo, Shinnar, Rani, Singh, Joseph, Sirven, Michael, Smith, Joe, Sullivan, Liu Lin, Thio, Anu, Venkat, Eileen, Vining, Gretchen, von Allmen, Judith, Weisenberg, Peter, Widdess-Walsh, Andrew, Yourich
Publikováno v:
Clinical trials (London, England). 10(4)
Background Epilepsy is a common neurological disorder that affects approximately 50 million people worldwide. Both risk of epilepsy and response to treatment partly depend on genetic factors, and gene identification is a promising approach to target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61c0fed6c19f938e92593466c0cc3bbd
https://pubmed.ncbi.nlm.nih.gov/23818435
https://pubmed.ncbi.nlm.nih.gov/23818435