Publikationen

2019

Luisa Olschewski, Silvia Jesús, Han-Joon Kim, Sinem Tunc, Sebastian Löns, Johanna Junker, Kirsten E. Zeuner, Andrea A. Kühn, Gregor Kuhlenbäumer, Eva Schäffer, Daniela Berg, Meike Kasten, Andreas Ferbert, Eckart Altenmüller, Norbert Brüggemann, Peter Bauer, Arndt Rolfs, Beomseok Jeon, Tobias Bäumer, Pablo Mir, Christine Klein, and Katja Lohmann,
Role of ANO3 mutations in dystonia: A large-scale mutational screening study, Parkinsonism Relat Disord , vol. 62, pp. 196–200, 2019.
DOI:10.1016/j.parkreldis.2018.12.030
Mayke Oosterloo, Emilia K. Bijlsma, Sander Mj van Kuijk, Floor Minkels, and Christine Em de Die-Smulders,
Clinical and genetic characteristics of late-onset Huntington’s disease, Parkinsonism Relat Disord , vol. 61, pp. 101–105, 2019.
DOI:10.1016/j.parkreldis.2018.11.009
Vanessa Petruo, Benjamin Bodmer, Valerie C. Brandt, Leoni Baumung, Veit Roessner, Alexander Münchau, and Christian Beste,
Altered perception-action binding modulates inhibitory control in Gilles de la Tourette syndrome, J Child Psychol Psychiatry , vol. 60, no. 9, pp. 953–962, 2019.
DOI:10.1111/jcpp.12938
Tim W. Rattay, Tobias Lindig, Jonathan Baets, Katrien Smets, Tine Deconinck, Anne S. Söhn, Konstanze Hörtnagel, Kathrin N. Eckstein, Sarah Wiethoff, Jennifer Reichbauer, Marion Döbler-Neumann, Ingeborg Krägeloh-Mann, Michaela Auer-Grumbach, Barbara Plecko, Alexander Münchau, Bernd Wilken, Marc Janauschek, Anne-Katrin Giese, Jan L. De Bleecker, Els Ortibus, Martine Debyser, Adolfo Lopez de Munain, Aurora Pujol, Maria Teresa Bassi, Maria Grazia D’Angelo, Peter De Jonghe, Stephan Züchner, Peter Bauer, Ludger Schöls, and Rebecca Schüle,
FAHN/SPG35: a narrow phenotypic spectrum across disease classifications, Brain , vol. 142, no. 6, pp. 1561–1572, 2019.
DOI:10.1093/brain/awz102
Armin Steffen, Wolfgang Jost, Tobias Bäumer, Dirk Beutner, Sabine Degenkolb-Weyers, Martin Groß, Maria Grosheva, Samer Hakim, Kai G. Kahl, Rainer Laskawi, Rebekka Lencer, Jan Löhler, Thekla Meyners, Saskia Rohrbach-Volland, Rainer Schönweiler, Sara-Christina Schröder, Sebastian Schröder, Heidrun Schröter-Morasch, Maria Schuster, Susanne Steinlechner, Roland Urban, and Orlando Guntinas-Lichius,
Hypersalivation: update of the German S2k guideline (AWMF) in short form, J Neural Transm (Vienna) , vol. 126, no. 7, pp. 853–862, 2019.
DOI:10.1007/s00702-019-02000-4
Joanne Trinh, Katja Lohmann, Hauke Baumann, Alexander Balck, Max Borsche, Norbert Brüggemann, Leon Dure, Marissa Dean, Jens Volkmann, Sinem Tunc, Jannik Prasuhn, Heike Pawlack, Sophie Imhoff, Christina M. Lill, Meike Kasten, Peter Bauer, Arndt Rolfs, [GROUP] International Parkinson’s Disease Genomics Consortium (IPDGC), and Christine Klein,
Utility and implications of exome sequencing in early-onset Parkinson’s disease, Mov Disord , vol. 34, no. 1, pp. 133–137, 2019.
DOI:10.1002/mds.27559
Sinem Tunc, Nastasja Baginski, Juliane Lubs, Julien F. Bally, Anne Weissbach, Magdalena Khira Baaske, Vera Tadic, Norbert Brüggemann, Tobias Bäumer, Christian Beste, and Alexander Münchau,
Predictive coding and adaptive behavior in patients with genetically determined cerebellar ataxia--A neurophysiology study, Neuroimage Clin , vol. 24, pp. 102043, 2019.
DOI:10.1016/j.nicl.2019.102043
Sinem Tunc, Jonas Denecke, Luisa Olschewski, Tobias Bäumer, Alexander Münchau, Davor Lessel, and Katja Lohmann,
A recurrent de-novo ANO3 mutation causes early-onset generalized dystonia, J Neurol Sci , vol. 396, pp. 199–201, 2019.
DOI:10.1016/j.jns.2018.11.024
Anne Weissbach, Kaviraja Udupa, Zhen Ni, Carolyn Gunraj, Cricia Rinchon, Julianne Baarbe, Alfonso Fasano, Renato P. Munhoz, Anthony Lang, Vera Tadic, Norbert Brüggemann, Alexander Münchau, Tobias Bäumer, and Robert Chen,
Single-pulse subthalamic deep brain stimulation reduces premotor-motor facilitation in Parkinson’s disease, Parkinsonism Relat Disord , vol. 66, pp. 224–227, 2019.
DOI:10.1016/j.parkreldis.2019.08.003
Anne Weissbach, Christina Wittke, Meike Kasten, and Christine Klein,
“Atypical” Parkinson’s disease - genetic, Int Rev Neurobiol , vol. 149, pp. 207–235, 2019.
DOI:10.1016/bs.irn.2019.10.011
Ana Westenberger, Charles Jourdan Reyes, Gerard Saranza, Valerija Dobricic, Henrike Hanssen, Aloysius Domingo, Björn-Hergen Laabs, Susen Schaake, Jelena Pozojevic, Aleksandar Raković, Karen Grütz, Kimberly Begemann, Uwe Walter, Dirk Dressler, Peter Bauer, Arndt Rolfs, Alexander Münchau, Frank J. Kaiser, Laurie J. Ozelius, Roland Dominic Jamora, Raymond L. Rosales, Cid Czarina E. Diesta, Katja Lohmann, Inke R. König, Norbert Brüggemann, and Christine Klein,
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism, Ann Neurol , vol. 85, no. 6, pp. 812–822, 2019.
DOI:10.1002/ana.25488
Anette Schrag, Davide Martino, Alan Apter, Juliane Ball, Erika Bartolini, Noa Benaroya-Milshtein, Maura Buttiglione, Francesco Cardona, Roberta Creti, Androulla Efstratiou, Maria Gariup, Marianthi Georgitsi, Tammy Hedderly, Isobel Heyman, Immaculada Margarit, Pablo Mir, Natalie Moll, Astrid Morer, Norbert Müller, Kirsten Müller-Vahl, Alexander Münchau, Graziella Orefici, Kerstin J. Plessen, Cesare Porcelli, Peristera Paschou, Renata Rizzo, Veit Roessner, Markus J. Schwarz, Tamar Steinberg, Friederike Tagwerker Gloor, Zsanett Tarnok, Susanne Walitza, Andrea Dietrich, Pieter J. Hoekstra, and [GROUP] EMTICS Collaborative Group,
European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents, Eur Child Adolesc Psychiatry , vol. 28, no. 1, pp. 91–109, 2019.
DOI:10.1007/s00787-018-1190-4
Max Borsche, Stefanie Hahn, Henrike Hanssen, Alexander Münchau, Klaus-Peter Wandinger, and Norbert Brüggemann,
Sez6l2-antibody-associated progressive cerebellar ataxia: a differential diagnosis of atypical parkinsonism, J Neurol , vol. 266, no. 2, pp. 522–524, 2019.
DOI:10.1007/s00415-018-9115-1
J. Prasuhn, K. Lohmann, H. Hanßen, Alexander Münchau, and N. Brüggemann,
Grenzen der Exomsequenzierung in der Diagnostik genetischer Erkrankungen, DGNeurologie , vol. 2, no. 2, pp. 109–112, 2019.
DOI:10.1007/s42451-018-0046-y
Stefan Hess, Petroula Mousikou, Julius Verrel, and Sascha Schroeder,
Syllabic processing in handwritten word production in German children and adults, Hum Mov Sci , vol. 65, pp. 5–14, 2019.
DOI:10.1016/j.humov.2018.07.003
Armin Steffen, Wolfgang Jost, Tobias Bäumer, Dirk Beutner, Sabine Degenkolb-Weyers, Martin Groß, Maria Grosheva, Samer Hakim, Kai G. Kahl, Rainer Laskawi, Rebekka Lencer, Jan Löhler, Thekla Meyners, Saskia Rohrbach-Volland, Rainer Schönweiler, Sara-Christina Schröder, Sebastian Schröder, Heidrun Schröter-Morasch, Maria Schuster, Susanne Steinlechner, Roland Urban, and Orlando Guntinas-Lichius,
[Hypersalivation - Update of the S2k guideline (AWMF) in short form], Laryngorhinootologie , vol. 98, no. 6, pp. 388–397, 2019.
DOI:10.1055/a-0874-2406
Alexander Münchau, Ludger Schöls, Christine Klein, and Holm Graessner,
[Model for personalized diagnostics and treatment in neurology-German Academy for Rare Neurological Diseases], Nervenarzt , vol. 90, no. 8, pp. 796–803, 2019.
DOI:10.1007/s00115-019-0750-2
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
Matt J. N. Brown, Anne Weissbach, Martje G. Pauly, Michael Vesia, Carolyn Gunraj, Julianne Baarbe, Alexander Münchau, Tobias Bäumer, and Robert Chen,
Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation, Brain Stimul , vol. 12, no. 5, pp. 1229–1243, 2019.
DOI:10.1016/j.brs.2019.04.009
Wolfgang H. Jost, Tobias Bäumer, Rainer Laskawi, Björn Spittau, Armin Steffen, and Martin Winterholler,
[Therapy of sialorrhea with botulinum toxin], Fortschr Neurol Psychiatr , vol. 87, no. 10, pp. 554–563, 2019.
DOI:10.1055/a-0958-2417
A. Koy, N. Bockhorn, A. A. Kühn, G.-H. Schneider, P. Krause, K. Lauritsch, K. Witt, S. Paschen, G. Deuschl, J. K. Krauss, A. Saryyeva, J. Runge, I. Borggraefe, J. H. Mehrkens, A. Horn, J. Vesper, A. Schnitzler, S. Siegert, M. Freilinger, M. Eckenweiler, V. A. Coenen, Vera Tadic, J. Voges, K. a. M. Pauls, J. Wirths, L. Timmermann, M. Hellmich, and [GROUP] GEPESTIM consortium,
Adverse events associated with deep brain stimulation in patients with childhood-onset dystonia, Brain Stimul , vol. 12, no. 5, pp. 1111–1120, 2019.
DOI:10.1016/j.brs.2019.04.003
Sebastian Löns,
KMT2B-Dystonie im Kindesalter – Häufigkeit und phänotypisches Spektrum, DGNeurologie , vol. 2, no. 6, pp. 510–512, 2019.
DOI:10.1007/s42451-019-00124-1
Wolfgang H. Jost, Tobias Bäumer, Rainer Laskawi, Jaroslaw Slawek, Björn Spittau, Armin Steffen, Martin Winterholler, and Ganesh Bavikatte,
Therapy of Sialorrhea with Botulinum Neurotoxin, Neurol Ther , vol. 8, no. 2, pp. 273–288, 2019.
DOI:10.1007/s40120-019-00155-6
Alexander Kleimaker, Maximilian Kleimaker, Christian Beste, Tobias Bäumer, and Alexander Münchau,
Somatosensory Processing in Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 238–242, 2019.
DOI:10.1024/1016-264X/a000273
Maximilian Kleimaker, Alexander Kleimaker, Christian Beste, Soyoung Q. Park, and Alexander Münchau,
Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 215–221, 2019.
DOI:10.1024/1016-264X/a000274
Shu-Chen Li, Roxane Dilcher, and Alexander Münchau,
Developmental Trajectories of Sensorimotor and Cognitive Control in Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 231–237, 2019.
DOI:10.1024/1016-264X/a000271
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
Adam Takacs, Annet Bluschke, Alexander Münchau, and Christian Beste,
Neuropharmacological Interventions and Event File Coding in Gilles de la Tourette Syndrome, Z Neuropsych , vol. 30, no. 4, pp. 223–229, 2019.
DOI:10.1024/1016-264X/a000270

2018

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
Christian Beste, Christian K. E. Moll, Monika Pötter-Nerger, and Alexander Münchau,
Striatal Microstructure and Its Relevance for Cognitive Control, Trends Cogn Sci , vol. 22, no. 9, pp. 747–751, 2018.
DOI:10.1016/j.tics.2018.06.007
Christian Beste, Moritz Mückschel, Raymond Rosales, Aloysius Domingo, Lillian Lee, Arlene Ng, Christine Klein, and Alexander Münchau,
The Basal Ganglia Striosomes Affect the Modulation of Conflicts by Subliminal Information-Evidence from X-Linked Dystonia Parkinsonism, Cereb Cortex , vol. 28, no. 7, pp. 2243–2252, 2018.
DOI:10.1093/cercor/bhx125
Christian Beste, and Alexander Münchau,
Tics and Tourette syndrome - surplus of actions rather than disorder?, Mov Disord , vol. 33, no. 2, pp. 238–242, 2018.
DOI:10.1002/mds.27244
Valerie C. Brandt, Johanna Hermanns, Christian Beck, Tobias Bäumer, Bartosz Zurowski, and Alexander Münchau,
The temporal relationship between premonitory urges and covert compulsions in patients with obsessive-compulsive disorder, Psychiatry Res , vol. 262, pp. 6–12, 2018.
DOI:10.1016/j.psychres.2018.01.041
Odette Fründt, Robert Schulz, Daniel Schöttle, Bastian Cheng, Götz Thomalla, Hanna Braass, Christos Ganos, Nicole David, Ina Peiker, Andreas K. Engel, Tobias Bäumer, and Alexander Münchau,
White Matter Microstructure of the Human Mirror Neuron System is Related to Symptom Severity in Adults with Autism, J Autism Dev Disord , vol. 48, no. 2, pp. 417–429, 2018.
DOI:10.1007/s10803-017-3332-9
H. A. Jinnah, Alberto Albanese, Kailash P. Bhatia, Francisco Cardoso, Gustavo Da Prat, Tom J. de Koning, Alberto J. Espay, Victor Fung, Pedro J. Garcia-Ruiz, Oscar Gershanik, Joseph Jankovic, Ryuji Kaji, Katya Kotschet, Connie Marras, Janis M. Miyasaki, Francesca Morgante, Alexander Münchau, Pramod Kumar Pal, Maria C. Rodriguez Oroz, Mayela Rodríguez-Violante, Ludger Schöls, Maria Stamelou, Marina Tijssen, Claudia Uribe Roca, Andres de la Cerda, Emilia M. Gatto, and [GROUP] International Parkinson’s Disease Movement Disorders Society Task Force on Rare Movement Disorders,
Treatable inherited rare movement disorders, Mov Disord , vol. 33, no. 1, pp. 21–35, 2018.
DOI:10.1002/mds.27140
Johanna Junker, Valerie Brandt, Brian D. Berman, Marie Vidailhet, Emmanuel Roze, Anne Weissbach, Cynthia Comella, Irene A. Malaty, Joseph Jankovic, Mark S. LeDoux, Alfredo Berardelli, Richard Barbano, Stephen G. Reich, Joel S. Perlmutter, H. A. Jinnah, and Norbert Brüggemann,
Predictors of alcohol responsiveness in dystonia, Neurology , vol. 91, no. 21, pp. e2020–e2026, 2018.
DOI:10.1212/WNL.0000000000006551
O. Kuseyri, Anne Weissbach, N. Brüggemann, C. Klein, M. Giżewska, D. Karall, S. Scholl-Bürgi, H. Romanowska, E. Krzywińska-Zdeb, A. A. Monavari, I. Knerr, Z. Yapıcı, V. Leuzzi, and T. Opladen,
Pregnancy management and outcome in patients with four different tetrahydrobiopterin disorders, J Inherit Metab Dis , vol. 41, no. 5, pp. 849–863, 2018.
DOI:10.1007/s10545-018-0169-0
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
Paul McNulty, Richard Pilcher, Raviram Ramesh, Renata Necuiniate, Alis Hughes, Daniel Farewell, Peter Holmans, Lesley Jones, and [GROUP] REGISTRY Investigators of the European Huntington’s Disease Network,
Reduced cancer incidence in Huntington’s disease: analysis in the Registry study, J Huntington Disease , vol. 7, no. 3, pp. 209–222, 2018.
Martje G. Pauly, Victor Krajka, Felix Stengel, Philip Seibler, Christine Klein, and Philipp Capetian,
Adherent vs. Free-Floating Neural Induction by Dual SMAD Inhibition for Neurosphere Cultures Derived from Human Induced Pluripotent Stem Cells, Front Cell Dev Biol , vol. 6, pp. 3, 2018.
DOI:10.3389/fcell.2018.00003
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
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
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
Andrew Sharott, Alessandro Gulberti, Wolfgang Hamel, Johannes A. Köppen, Alexander Münchau, Carsten Buhmann, Monika Pötter-Nerger, Manfred Westphal, Christian Gerloff, Christian K. E. Moll, and Andreas K. Engel,
Spatio-temporal dynamics of cortical drive to human subthalamic nucleus neurons in Parkinson’s disease, Neurobiol Dis , vol. 112, pp. 49–62, 2018.
DOI:10.1016/j.nbd.2018.01.001
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
Sinem Tunc, Vera Tadic, Christine Zühlke, Yorck Hellenbroich, and Norbert Brüggemann,
Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophy, Neurology , vol. 90, no. 3, pp. 142–143, 2018.
DOI:10.1212/WNL.0000000000004833
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
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
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