Univ.-Prof. Dr. med. Alexander Münchau

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

Eunju Seong, Ryan Insolera, Marija Dulovic, Erik-Jan Kamsteeg, Joanne Trinh, Norbert Brüggemann, Erin Sandford, Sheng Li, Ayse Bilge Ozel, Jun Z. Li, Tamison Jewett, Anneke J. A. Kievit, Alexander Münchau, Vikram Shakkottai, Christine Klein, Catherine A. Collins, Katja Lohmann, Bart P. van de Warrenburg, and Margit Burmeister,
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects, Ann Neurol , vol. 83, no. 6, pp. 1075–1088, 2018.

DOI:	10.1002/ana.25220

Humera Manzoor, Norbert Brüggemann, Hafiz Muhammad Jafar Hussain, Tobias Bäumer, Frauke Hinrichs, Muhammad Wajid, Alexander Münchau, Sadaf Naz, and Katja Lohmann,
Novel homozygous variants in ATCAY, MCOLN1, and SACS in complex neurological disorders, Parkinsonism Relat Disord , vol. 51, pp. 91–95, 2018.

DOI:	10.1016/j.parkreldis.2018.02.005

S. Zittel, Vera Tadic, C. K. E. Moll, Tobias Bäumer, A. Fellbrich, A. Gulberti, D. Rasche, N. Brüggemann, V. Tronnier, and Alexander Münchau,
Prospective evaluation of Globus pallidus internus deep brain stimulation in Huntington’s disease, Parkinsonism Relat Disord , vol. 51, pp. 96–100, 2018.

DOI:	10.1016/j.parkreldis.2018.02.030

Alexander Münchau,
Seltene neurologische Erkrankungen, Nervenheilkunde , vol. 37, no. 03, pp. 119–121, 2018.

DOI:	10.1055/s-0038-1642085