Prof. Dr. med. Anne Weissbach

Universität zu Lübeck
Universitätsklinikum Schleswig-Holstein, Campus Lübeck
Ratzeburger Allee 160
23562 Lübeck
Gebäude CBBM (Haus 66),
Raum 040,3.OG
Email: | anne.weissbach(at)uni-luebeck.de |
Phone: | 0451 500 43452 |
Fax: | 0451 3101 8225 |
Publikationen
2017
Anne
Weissbach,
Elisa
Werner,
Julien F.
Bally,
Sinem
Tunc,
Sebastian
Löns,
Dagmar
Timmann,
Kirsten E.
Zeuner,
Vera
Tadic,
Norbert
Brüggemann,
Anthony
Lang,
Christine
Klein,
Alexander
Münchau, and
Tobias
Bäumer,
Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation, Ann Neurol , vol. 82, no. 4, pp. 543–553, 2017.
Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation, Ann Neurol , vol. 82, no. 4, pp. 543–553, 2017.
DOI: | 10.1002/ana.25035 |
Ana
Westenberger,
Christoph
Max,
Norbert
Brüggemann,
Aloysius
Domingo,
Karen
Grütz,
Heike
Pawlack,
Anne
Weissbach,
Andrea A.
Kühn,
Juliane
Spiegler,
Anthony E.
Lang,
Jürgen
Sperner,
Victor S. C.
Fung,
Jens
Schallner,
Gabriele
Gillessen-Kaesbach,
Alexander
Münchau, and
Christine
Klein,
Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases, J Pediatr , vol. 181, pp. 306-308.e1, 2017.
Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases, J Pediatr , vol. 181, pp. 306-308.e1, 2017.
DOI: | 10.1016/j.jpeds.2016.10.079 |
Karen
Grütz,
Philip
Seibler,
Anne
Weissbach,
Katja
Lohmann,
Francesca A.
Carlisle,
Derek J.
Blake,
Ana
Westenberger,
Christine
Klein, and
Anne
Grünewald,
Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia, Sci Rep , vol. 7, pp. 41156, 2017.
Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia, Sci Rep , vol. 7, pp. 41156, 2017.
DOI: | 10.1038/srep41156 |
Eva
Hebert,
Friederike
Borngräber,
Alexander
Schmidt,
Aleksandar
Raković,
Ingrid
Brænne,
Anne
Weissbach,
Jennie
Hampf,
Eva-Juliane
Vollstedt,
Leopold
Größer,
Susen
Schaake,
Michaela
Müller,
Humera
Manzoor,
Hans-Christian
Jabusch,
Daniel
Alvarez-Fischer,
Meike
Kasten,
Vladimir S.
Kostić,
Thomas
Gasser,
Kirsten E.
Zeuner,
Han-Joon
Kim,
Beomseok
Jeon,
Peter
Bauer,
Eckart
Altenmüller,
Christine
Klein, and
Katja
Lohmann,
Functional Characterization of Rare RAB12 Variants and Their Role in Musician’s and Other Dystonias, Genes , vol. 8, no. 10, pp. 276, 2017.
Functional Characterization of Rare RAB12 Variants and Their Role in Musician’s and Other Dystonias, Genes , vol. 8, no. 10, pp. 276, 2017.
DOI: | 10.3390/genes8100276 |
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
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 |
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 |
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 |