2014

Dejanovic, B., D. Lal, C. B. Catarino, S. Arjune, A. A. Belaidi, H. Trucks, C. Vollmar, R. Surges, W. S. Kunz, S. Motameny, J. Altmuller, A. Kohler, B. A. Neubauer, Consortium Epicure, P. Nurnberg, S. Noachtar, G. Schwarz, and T. Sander. Exonic Microdeletions of the Gephyrin Gene Impair Gabaergic Synaptic Inhibition in Patients with Idiopathic Generalized Epilepsy. Neurobiol Dis 67,  (2014): 88-96.

Wilbrand J-F, Bierther U, Nord T, Reinges M, Hahn A, Christophis P, Streckbein P, Kähling C, Howaldt HP. Hahn A, Howaldt, . Percentile-based assessment of craniosynostosis. Journal of Cranio-Maxillofacial Surgery, 2014, 42: 634-640

Schänzer A, Döring B, Ondrouschek M, Goos S, Garvalov BK, Geyer G, Acker T, Neubauer B, Hahn A. Stress induced up-regulation of SLC19A3 is impaired in patients with thiamine transporter 2 deficiency. Brain Pathol, 2014, 24:270-299

Neubauer BA, Hahn A. Syndromes at risk for status epilepticus in children. Epileptic Disord 2014, Suppl 1: 89-95

Lal D, Reinthaler EM, Schubert J, Muhle H, Riesch E, Kluger G, Jabbari K, Kawalia A, Bäumel C, Holthausen H, Hahn A, Feucht M, Neophytou B, Haberlandt E, Becker F, Altmüller J, Thiele H, Lemke JR, Lerche H, Nürnberg P, Sander T, Weber Y, Zimprich F, Neubauer BA. DEPDC5 mutations in genetic focal epilepsies of childhood. Ann Neurol. 2014, 75: 788-792

Feustel A, Hahn A*, Schneider C, Reichenberger F, Sieweke N, Farahmad P, Franzen W, Kaps M, Rolfs A, Tanislav C. Continuous cardiac troponin release in patients with Fabry disease. PLoS1 2014, 9: e91757

Hahn A. Metabolische Epilepsien im Kindes- und Jugendalter. Z Epileptol 2014, 27: 170-177.

Reinthaler EM, Lal D, Lebon S, Hildebrand MS, Feucht M, Steinböck H, Hahn A, Neophythou B, Ronen G, Roche L, Gruber-Sedlmayr U, Geldner J, Haberlandt E, Hoffmann P, Herms S, Gieger C, Waldenberger M, Franke A, Wittig M, Schoch McGovern S, Becker AJ, Männik K, Winterer G, Toliat M, Lerche H, Nürnberg P, Mefford M, Scheffer IE, Beckmann JS, EPICURE Consortium, Sander T, Jacquemont S, Reymond A F, Neubauer BA, Zimprich. Analysis of ELP4, SRPX2 and interacting genes in typical and atypical Rolandic epilepsy. Epilepsia 2014, 55: e89-93

Reinthaler EM, Lal D, Lebon S, Hildebrand MS, Feucht M, Steinböck H, Hahn A, Neophythou B, Ronen G, Roche L, Gruber-Sedlmayr U, Geldner J, Haberlandt E, Hoffmann P, Herms S, Gieger C, Waldenberger M, Franke A, Wittig M, Schoch McGovern S, Becker AJ, Männik K, Winterer G, Toliat M, Lerche H, Nürnberg P, Mefford M, Scheffer IE, Beckmann JS, EPICURE Consortium, Sander T, Jacquemont S, Reymond A, Zimprich F, Neubauer BA. 16p11.2 600 kb duplications confer risk for typical and atypical Rolandic epilepsy. Hum Mol Genet 2014, 23: 6069-6080

Reinthaler EM, Lal D, Jurkowski W, Feucht M, Steinböck H, Gruber-Sedlmayr U, Ronen GM, Geldner J, Haberlandt E, Neophytou B, Hahn A, Altmüller J, Thiele H, Toliat MR; EuroEPINOMICS Consortium, Lerche H, Nürnberg P, Sander T, Neubauer BA, Zimprich F. Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy. Epilepsia. 2014 Aug;55(8):e89-93. doi: 10.1111/epi.12712. Epub 2014 Jul 3.

Steiß JO, Durschnabel M, Hamscho N, Burchert D, Hahn A, Weidner W, Altinkilic B. Nierenkarbunkel und perinephritischer Abszess im Kindes- und Jugendalter. Der Urologe 2014, 53: 1476-81