Department of Neurology

Serotonin transporter gene and stress reactivity in unipolar depression : Role of the HPA system as endophenotype of the SLC6A4 gene (2014) Welper H, Aller A, Guttenthaler V, Hoefels S, Lennertz L, Pfeiffer U, Schwab S, Zobel A Journal article Impaired renal function in stroke patients with atrial fibrillation (2014) Sauer EM, Sauer R, Kallmuenzer B, Blinzler C, Breuer L, Huttner H, Schwab S, Köhrmann M Journal article Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice (2014) Casadei N, Pöhler AM, Tomas-Zapico C, Torres-Peraza J, Schwedhelm I, Witz A, Zamolo I, et al. Journal article The small GTPase Rab11 co-localizes with ?-synuclein in intracellular inclusions and modulates its aggregation, secretion and toxicity (2014) Chutna O, Goncalves S, Villar-Pique A, Guerreiro P, Marijanovic Z, Mendes T, Ramalho J, et al. Journal article 7T MRI features in control human hippocampus and hippocampal sclerosis: An ex vivo study with histologic correlations (2014) Coras R, Milesi G, Zucca I, Mastropietro A, Scotti A, Figini M, Muehlebner A, et al. Journal article Improved resection in lesional temporal lobe epilepsy surgery using neuronavigation and intraoperative MR imaging: Favourable long term surgical and seizure outcome in 88 consecutive cases (2014) Roessler K, Sommer B, Grummich P, Coras R, Kasper B, Hamer H, Blümcke I, et al. Journal article Frameless stereotactic functional neuronavigation combined with intraoperative magnetic resonance imaging as a strategy in highly eloquent located tumors causing epilepsy (2014) Sommer B, Grummich P, Hamer H, Blümcke I, Coras R, Buchfelder M, Roessler K Journal article Behandlung nach dem ersten Anfall? Pro (2014) Hamer H Journal article Comprehensive visualization of paresthesia in breast cancer survivors (2014) Jud S, Hatko R, Maihoefner C, Bani M, Schrauder MG, Lux MP, Beckmann M, et al. Journal article A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotype (2014) Leal A, Berghoff C, Berghoff M, Rojas-Araya M, Ortiz C, Heuss D, Del Valle G, Rautenstrauß B Journal article