Priv. doz. Dr. med. Anne Weissbach

Photo of Anne  Weissbach

University of Lübeck
University Medical Center Schleswig-Holstein, Campus Lübeck
Ratzeburger Allee 160
23562 Lübeck

Gebäude CBBM (Building 66), Raum 040,3rd Floor

Email: anne.weissbach(at)uni-luebeck.de
Phone: +49 451 500 43452
Fax: +49 451 3101 8225

Publications

2017

Anne Weissbach, Inke R. König, Katja Hückelheim, Peter P. Pramstaller, Elisa Werner, Norbert Brüggemann, Vera Tadic, Katja Lohmann, Tobias Bäumer, Alexander Münchau, Meike Kasten, and Christine Klein,
Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers, Parkinsonism Relat Disord , vol. 42, pp. 95–99, 2017.
DOI:10.1016/j.parkreldis.2017.07.003

2016

Mark S. LeDoux, Satya R. Vemula, Jianfeng Xiao, Misty M. Thompson, Joel S. Perlmutter, Laura J. Wright, H. A. Jinnah, Ami R. Rosen, Peter Hedera, Cynthia L. Comella, Anne Weissbach, Johanna Junker, Joseph Jankovic, Richard L. Barbano, Stephen G. Reich, Ramon L. Rodriguez, Brian D. Berman, Sylvain Chouinard, Lawrence Severt, Pinky Agarwal, and Natividad P. Stover,
Clinical and genetic features of cervical dystonia in a large multicenter cohort, Neurol Genet , vol. 2, no. 3, pp. e69, 2016.
DOI:10.1212/NXG.0000000000000069
Eva Koschmidder, Anne Weissbach, Norbert Brüggemann, Meike Kasten, Christine Klein, and Katja Lohmann,
A nonsense mutation in CHCHD2 in a patient with Parkinson disease, Neurology , vol. 86, no. 6, pp. 577–579, 2016.
DOI:10.1212/WNL.0000000000002361

2015

Niccolò E. Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, Friedrich Asmus, Marthe H. R. Ludtmann, Mina Ryten, Vincent Plagnol, Ann-Kathrin Hauser, Sara Bandres-Ciga, Conceição Bettencourt, Paola Forabosco, Deborah Hughes, Marc M. P. Soutar, Kathryn Peall, Huw R. Morris, Daniah Trabzuni, Mehmet Tekman, Horia C. Stanescu, Robert Kleta, Miryam Carecchio, Giovanna Zorzi, Nardo Nardocci, Barbara Garavaglia, Ebba Lohmann, Anne Weissbach, Christine Klein, John Hardy, Alan M. Pittman, Thomas Foltynie, Andrey Y. Abramov, Thomas Gasser, Kailash P. Bhatia, and Nicholas W. Wood,
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia, Am J Hum Genet , vol. 96, no. 6, pp. 938–947, 2015.
DOI:10.1016/j.ajhg.2015.04.008
Anne Weissbach, Tobias Bäumer, Raymond Rosales, Lillian V. Lee, Norbert Brüggemann, Aloysius Domingo, Ana Westenberger, Roland D. Jamora, Cid C. Diesta, Valerie Brandt, Vera Tadic, Simone Zittel, Christine Klein, and Alexander Münchau,
Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease, Mov Disord , vol. 30, no. 6, pp. 873–875, 2015.
DOI:10.1002/mds.26224
Anne Weissbach, Tobias Bäumer, Norbert Brüggemann, Vera Tadic, Simone Zittel, Bastian Cheng, Götz Thomalla, Christine Klein, and Alexander Münchau,
Premotor-motor excitability is altered in dopa-responsive dystonia, Mov Disord , vol. 30, no. 12, pp. 1705–1709, 2015.
DOI:10.1002/mds.26365
Niccolò E. Mencacci, Léa R’bibo, Sara Bandres-Ciga, Miryam Carecchio, Giovanna Zorzi, Nardo Nardocci, Barbara Garavaglia, Amit Batla, Kailash P. Bhatia, Alan M. Pittman, John Hardy, Anne Weissbach, Christine Klein, Thomas Gasser, Ebba Lohmann, and Nicholas W. Wood,
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort, Hum Mol Genet , vol. 24, no. 18, pp. 5326–5329, 2015.
DOI:10.1093/hmg/ddv255

2014

Anne Weissbach, and Christine Klein,
Hereditary dystonia and parkinsonism: two sides of the same coin?, Brain , vol. 137, no. Pt 9, pp. 2402–2404, 2014.
DOI:10.1093/brain/awu181
Franca Vulinovic, Katja Lohmann, Aleksandar Raković, Philipp Capetian, Daniel Alvarez-Fischer, Alexander Schmidt, Anne Weissbach, Alev Erogullari, Frank J. Kaiser, Karin Wiegers, Andreas Ferbert, Arndt Rolfs, Christine Klein, and Philip Seibler,
Unraveling cellular phenotypes of novel TorsinA/TOR1A mutations, Hum Mutat , vol. 35, no. 9, pp. 1114–1122, 2014.
DOI:10.1002/humu.22604

2013

Anne Weissbach, Meike Kasten, Anne Grünewald, Norbert Brüggemann, Peter Trillenberg, Christine Klein, and Johann Hagenah,
Prominent psychiatric comorbidity in the dominantly inherited movement disorder myoclonus-dystonia, Parkinsonism Relat Disord , vol. 19, no. 4, pp. 422–425, 2013.
DOI:10.1016/j.parkreldis.2012.12.004