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Page 1
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K, Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn JA, Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, Vaher U, Talvik T, Dimova P, Guerrero López R, Serratosa JM, Linnankivi T, Lehesjoki AE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, Kurlemann G, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Sperner J, Becker F, Weber YG, Feucht M, Steinböck H, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J, Harvey RJ, Hoffmann P, Herms S, Altmüller J, Toliat MR, Thiele H, Nürnberg P, Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, von Spiczak S. Lemke JR, et al. Among authors: hahn a. Nat Genet. 2013 Sep;45(9):1067-72. doi: 10.1038/ng.2728. Epub 2013 Aug 11. Nat Genet. 2013. PMID: 23933819
Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family study.
Doose H, Hahn A, Neubauer BA, Pistohl J, Stephani U. Doose H, et al. Among authors: hahn a. Neuropediatrics. 2001 Feb;32(1):9-13. doi: 10.1055/s-2001-12215. Neuropediatrics. 2001. PMID: 11315204
Three fathers reported grand mal. In 29 families of the series of Hahn et al EEG recordings were performed: 22 brothers, 19 sisters and 16 pairs of parents. ...Photoparoxysmal response and generalized spikes and waves during rest and hyperventilation were also found to be …
Three fathers reported grand mal. In 29 families of the series of Hahn et al EEG recordings were performed: 22 brothers, 19 sisters a …
Clinical spectrum and genetics of Rolandic epilepsy.
Neubauer BA, Hahn A, Stephani U, Doose H. Neubauer BA, et al. Among authors: hahn a. Adv Neurol. 2002;89:475-9. Adv Neurol. 2002. PMID: 11968472 Review. No abstract available.
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.
Senderek J, Bergmann C, Stendel C, Kirfel J, Verpoorten N, De Jonghe P, Timmerman V, Chrast R, Verheijen MH, Lemke G, Battaloglu E, Parman Y, Erdem S, Tan E, Topaloglu H, Hahn A, Müller-Felber W, Rizzuto N, Fabrizi GM, Stuhrmann M, Rudnik-Schöneborn S, Züchner S, Michael Schröder J, Buchheim E, Straub V, Klepper J, Huehne K, Rautenstrauss B, Büttner R, Nelis E, Zerres K. Senderek J, et al. Among authors: hahn a. Am J Hum Genet. 2003 Nov;73(5):1106-19. doi: 10.1086/379525. Epub 2003 Oct 21. Am J Hum Genet. 2003. PMID: 14574644 Free PMC article.
Photosensitivity: genetics and clinical significance.
Neubauer BA, Waltz S, Grothe M, Hahn A, Tuxhorn I, Sander T, Kurlemann G, Stephani U. Neubauer BA, et al. Among authors: hahn a. Adv Neurol. 2005;95:217-26. Adv Neurol. 2005. PMID: 15508925 No abstract available.
[Autism and metabolic disorders-a rational approach].
Hahn A, Neubauer BA. Hahn A, et al. Z Kinder Jugendpsychiatr Psychother. 2005 Oct;33(4):259-71. doi: 10.1024/1422-4917.33.4.259. Z Kinder Jugendpsychiatr Psychother. 2005. PMID: 16294704 Review. German.
1,857 results