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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...American journal of human genetics, 2014-10, Vol.95 (4), p.360-370
- Appenzeller, Silke
- Balling, Rudi
- Barisic, Nina
- Baulac, Stéphanie
- Caglayan, Hande
- De Jonghe, Peter
- Depienne, Christel
- Dimova, Petia
- Djémié, Tania
- Gormley, Padhraig
- Guerrini, Renzo
- Helbig, Ingo
- Hjalgrim, Helle
- Jähn, Johanna
- Klein, Karl Martin
- Koeleman, Bobby
- Komarek, Vladimir
- Krause, Roland
- Kuhlenbäumer, Gregor
- Lemke, Johannes R.
- Lerche, Holger
- Linnankivi, Tarja
- Marini, Carla
- May, Patrick
- Møller, Rikke S.
- Muhle, Hiltrud
- Palotie, Aarno
- Pendziwiat, Manuela
- Roelens, Filip
- Rosenow, Felix
- Selmer, Kaja
- Serratosa, Jose M.
- Sisodiya, Sanjay
- Stephani, Ulrich
- Sterbova, Katalin
- Striano, Pasquale
- Suls, Arvid
- Talvik, Tiina
- von Spiczak, Sarah
- Weckhuysen, Sarah
- Abou-Khalil, Bassel
- Alldredge, Brian K.
- Andermann, Eva
- Andermann, Frederick
- Amron, Dina
- Bautista, Jocelyn F.
- Berkovic, Samuel F.
- Bluvstein, Judith
- Boro, Alex
- Consalvo, Damian
- Crumrine, Patricia
- Devinsky, Orrin
- Dlugos, Dennis
- Epstein, Michael P.
- Fiol, Miguel
- French, Jacqueline
- Friedman, Daniel
- Geller, Eric B.
- Glauser, Tracy
- Glynn, Simon
- Haas, Kevin
- Haut, Sheryl R.
- Hayward, Jean
- Helmers, Sandra L.
- Joshi, Sucheta
- Kanner, Andres
- Knowlton, Robert C.
- Kossoff, Eric H.
- Kuperman, Rachel
- Kuzniecky, Ruben
- Lowenstein, Daniel H.
- Motika, Paul V.
- Novotny, Edward J.
- Ottman, Ruth
- Paolicchi, Juliann M.
- Parent, Jack
- Park, Kristen
- Scheffer, Ingrid E.
- Shellhaas, Renée A.
- Sherr, Elliott
- Singh, Rani
- Smith, Michael C.
- Sullivan, Joe
- Venkat, Anu
- Vining, Eileen P.G.
- Von Allmen, Gretchen K.
- Weisenberg, Judith L.
- Winawer, Melodie R.
- Cossette, Patrick
- Delanty, Norman
- Eichler, Evan E.
- Goldstein, David B.
- Han, Yujun
- Heinzen, Erin L.
- Marson, Anthony G.
- Nieh, Sahar Esmaeeli
- O’Brien, Terence J.
- Petrou, Stephen
- Petrovski, Slavé
- Ruzzo, Elizabeth K.
2014
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Nature genetics, 2015-04, Vol.47 (4), p.393-399
- Syrbe, Steffen
- Hedrich, Ulrike B S
- Riesch, Erik
- Djémié, Tania
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2015
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American journal of human genetics, 2018-12, Vol.103 (6), p.1022-1029
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- Selmer, Kaja
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- Lemke, Johannes
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2018
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American journal of human genetics, 2019-06, Vol.104 (6), p.1060-1072
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- Palotie, Aarno
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2019
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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
- Chatron, Nicolas
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2020
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Orphanet journal of rare diseases, 2018-05, Vol.13 (1), p.71-71, Article 71
2018
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Epilepsy research, 2019-10, Vol.156, p.106181-106181, Article 106181
2019
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BMC medical genetics, 2017-06, Vol.18 (1), p.62-62, Article 62
2017
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Genetics in medicine, 2019-04, Vol.21 (4), p.837-849
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2019
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Neurology, 2023-02, Vol.100 (6), p.e603
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2023
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Italian journal of pediatrics, 2023-01, Vol.49 (1), p.11-10, Article 11
2023
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Genetic testing and molecular biomarkers, 2017-10, Vol.21 (10), p.613-618
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American journal of human genetics, 2017-01, Vol.100 (1), p.179-179
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2017
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American journal of medical genetics. Part A, 2023-03, Vol.191 (3), p.870-877
2023
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American journal of medical genetics. Part A, 2021-05, Vol.185 (5), p.1363-1365
2021
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European journal of medical genetics, 2021-09, Vol.64 (9), p.104263-104263, Article 104263
2021
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Brain (London, England : 1878), 2018-11, Vol.141 (11), p.3160-3178
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American journal of human genetics, 2015-05, Vol.96 (5), p.808-815
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2015
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Journal of medical genetics, 2016-08, Vol.53 (8), p.511-522
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Neuropediatrics, 2018-06, Vol.49 (3), p.204-208
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Neuropediatrics, 2019-02, Vol.50 (1), p.57-60
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Brain (London, England : 1878), 2022-09, Vol.145 (9), p.2991-3009
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Neurology, 2015-02, Vol.84 (5), p.480-489
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American journal of human genetics, 2013-11, Vol.93 (5), p.967-975
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Volltextzugriff (PDF)
Epilepsia (Copenhagen), 2020-05, Vol.61 (5), p.995-1007
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