Univ.-Prof. Dr. med. Alexander Münchau

Alexander Münchau, and Christian Beste,
Sonderheft – Gilles de la Tourette Syndrom, Z Neuropsych , vol. 30, no. 4, pp. 213–214, 2019.

DOI:	10.1024/1016-264X/a000269

Sinem Tunc, Marija Dulovic-Mahlow, Hauke Baumann, Magdalena Khira Baaske, Magdalena Jahn, Johanna Junker, Alexander Münchau, Norbert Brüggemann, and Katja Lohmann,
Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2, Cerebellum , vol. 18, no. 4, pp. 817–822, 2019.

DOI:	10.1007/s12311-019-01036-2

N. H. Jung, Alexander Münchau, and V. Mall,
[Neuronal plasticity and neuromodulation in pediatric neurology], Nervenarzt , vol. 89, no. 10, pp. 1131–1139, 2018.

DOI:	10.1007/s00115-018-0586-1

Jennifer Tübing, Bettina Gigla, Valerie Cathérine Brandt, Julius Verrel, Anne Weissbach, Christian Beste, Alexander Münchau, and Tobias Bäumer,
Associative plasticity in supplementary motor area - motor cortex pathways in Tourette syndrome, Sci Rep , vol. 8, no. 1, pp. 11984, 2018.

DOI:	10.1038/s41598-018-30504-8

L. Schöls, T. Gasser, I. Krägeloh-Mann, H. Graessner, T. Klockgether, and Alexander Münchau,
Centers for Rare Neurological Diseases, Aktuel Neurol , vol. 45, no. 3, pp. 178–186, 2018.

DOI:	10.1055/s-0043-114000

L. Schöls, H. Graessner, and Alexander Münchau,
Deutsche Akademie für Seltene Neurologische Erkrankungen, Nervenheilkunde , vol. 37, no. 03, pp. 136–141, 2018.

DOI:	10.1055/s-0038-1642087

Hauke Baumann, Magdalena Jahn, Alexander Münchau, Michaela Trilck-Winkler, Katja Lohmann, and Philip Seibler,
Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriers, Stem Cell Res , vol. 33, pp. 60–64, 2018.

DOI:	10.1016/j.scr.2018.09.018

Mohamed Abdulkadir, Douglas Londono, Derek Gordon, Thomas V. Fernandez, Lawrence W. Brown, Keun-Ah Cheon, Barbara J. Coffey, Lonneke Elzerman, Carolin Fremer, Odette Fründt, Blanca Garcia-Delgar, Donald L. Gilbert, Dorothy E. Grice, Tammy Hedderly, Isobel Heyman, Hyun Ju Hong, Chaim Huyser, Laura Ibanez-Gomez, Ewgeni Jakubovski, Young Key Kim, Young Shin Kim, Yun-Joo Koh, Sodahm Kook, Samuel Kuperman, Bennett Leventhal, Andrea G. Ludolph, Marcos Madruga-Garrido, Athanasios Maras, Pablo Mir, Astrid Morer, Kirsten Müller-Vahl, Alexander Münchau, Tara L. Murphy, Kerstin J. Plessen, Veit Roessner, Eun-Young Shin, Dong-Ho Song, Jungeun Song, Jennifer Tübing, Els van den Ban, Frank Visscher, Sina Wanderer, Martin Woods, Samuel H. Zinner, Robert A. King, Jay A. Tischfield, Gary A. Heiman, Pieter J. Hoekstra, and Andrea Dietrich,
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach, Eur Arch Psychiatry Clin Neurosci , vol. 268, no. 3, pp. 301–316, 2018.

DOI:	10.1007/s00406-017-0808-8

Philip Seibler, Lena F. Burbulla, Marija Dulovic, Simone Zittel, Johanne Heine, Thomas Schmidt, Franziska Rudolph, Ana Westenberger, Aleksandar Raković, Alexander Münchau, Dimitri Krainc, and Christine Klein,
Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells, Brain , vol. 141, no. 10, pp. 3052–3064, 2018.

DOI:	10.1093/brain/awy230

J. Tübing, J. Bohnenpoll, J. Spiegler, G. Gillessen-Kaesbach, Tobias Bäumer, C. Max, J. Sperner, C. Klein, and Alexander Münchau,
Methylphenidate Can Improve Chorea in NKX2.1 and ADCY5 Mutation-positive Patients-A Report of Two Children, Mov Disord Clin Pract , vol. 5, no. 3, pp. 343–345, 2018.

DOI:	10.1002/mdc3.12608