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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Syrbe S, Hedrich UBS, Riesch E, Djémié T, Müller S, Møller RS, Maher B, Hernandez-Hernandez L, Synofzik M, Caglayan HS, Arslan M, Serratosa JM, Nothnagel M, May P, Krause R, Löffler H, Detert K, Dorn T, Vogt H, Krämer G, Schöls L, Mullis PE, Linnankivi T, Lehesjoki AE, Sterbova K, Craiu DC, Hoffman-Zacharska D, Korff CM, Weber YG, Steinlin M, Gallati S, Bertsche A, Bernhard MK, Merkenschlager A, Kiess W; EuroEPINOMICS RES consortium; Gonzalez M, Züchner S, Palotie A, Suls A, De Jonghe P, Helbig I, Biskup S, Wolff M, Maljevic S, Schüle R, Sisodiya SM, Weckhuysen S, Lerche H, Lemke JR. Syrbe S, et al. Among authors: kiess w. Nat Genet. 2015 Apr;47(4):393-399. doi: 10.1038/ng.3239. Epub 2015 Mar 9. Nat Genet. 2015. PMID: 25751627 Free PMC article.
Modulation of arousal reaction in children with nocturnal enuresis.
Limbach A, Hückel D, Gelbrich G, Merkenschlager A, Kiess W, Keller E. Limbach A, et al. Among authors: kiess w. Klin Padiatr. 2007 Jul-Aug;219(4):230-3. doi: 10.1055/s-2007-971048. Klin Padiatr. 2007. PMID: 17638169 No abstract available.
[Retrospective analysis of 44 childhood drowning accidents].
Brüning C, Siekmeyer W, Siekmeyer M, Merkenschlager A, Kiess W. Brüning C, et al. Among authors: kiess w. Wien Klin Wochenschr. 2010 Jul;122(13-14):405-12. doi: 10.1007/s00508-010-1400-7. Epub 2010 Jul 8. Wien Klin Wochenschr. 2010. PMID: 20602279 German.
A rare case of congenital choroid plexus carcinoma.
Wilhelm M, Hirsch W, Merkenschlager A, Stepan H, Geyer C, Kiess W. Wilhelm M, et al. Among authors: kiess w. Pediatr Hematol Oncol. 2012 Oct;29(7):643-6. doi: 10.3109/08880018.2012.710298. Epub 2012 Aug 10. Pediatr Hematol Oncol. 2012. PMID: 22881717
857 results