Priv. doz. Dr. med. 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 |