Univ.-Prof. Dr. med. Alexander Münchau

Universität zu Lübeck
Universitätsklinikum Schleswig-Holstein, Campus Lübeck
Ratzeburger Allee 160
23562 Lübeck
Gebäude CBBM (Haus 66),
Raum 012,2.OG
Email: | alexander.muenchau(at)uni-luebeck.de |
Phone: | 0451 3101 8215 |
Fax: | 0451 3101 8225 |
Publikationen
2019
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.
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 |
Valentina
Niccolai,
Silvana
Korczok,
Jennifer
Finis,
Melanie
Jonas,
Götz
Thomalla,
Hartwig Roman
Siebner,
Kirsten
Müller-Vahl,
Alexander
Münchau,
Alfons
Schnitzler, and
Katja
Biermann-Ruben,
A peek into premonitory urges in Tourette syndrome: Temporal evolution of neurophysiological oscillatory signatures, Parkinsonism Relat Disord , vol. 65, pp. 153–158, 2019.
A peek into premonitory urges in Tourette syndrome: Temporal evolution of neurophysiological oscillatory signatures, Parkinsonism Relat Disord , vol. 65, pp. 153–158, 2019.
DOI: | 10.1016/j.parkreldis.2019.05.039 |
Darius
Ebrahimi-Fakhari,
Alexander
Münchau, and
Maria
Stamelou,
A special issue on childhood-onset movement disorders, Mov Disord , vol. 34, no. 5, pp. 595–597, 2019.
A special issue on childhood-onset movement disorders, Mov Disord , vol. 34, no. 5, pp. 595–597, 2019.
DOI: | 10.1002/mds.27663 |
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.
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 |
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.
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 |
Henrike
Hanssen,
Julia
Steinhardt,
Alexander
Münchau,
Arkan
Al-Zubaidi,
Elinor
Tzvi,
Marcus
Heldmann,
Peter
Schramm,
Alexander
Neumann,
Dirk
Rasche,
Assel
Saryyeva,
Jürgen
Voges,
Imke
Galazky,
Lars
Büntjen,
Hans-Jochen
Heinze,
Joachim K.
Krauss,
Volker
Tronnier,
Thomas F.
Münte, and
Norbert
Brüggemann,
Cerebello-striatal interaction mediates effects of subthalamic nucleus deep brain stimulation in Parkinson’s disease, Parkinsonism Relat Disord , vol. 67, pp. 99–104, 2019.
Cerebello-striatal interaction mediates effects of subthalamic nucleus deep brain stimulation in Parkinson’s disease, Parkinsonism Relat Disord , vol. 67, pp. 99–104, 2019.
DOI: | 10.1016/j.parkreldis.2019.09.003 |
Christine
Klein,
Hauke
Baumann,
Luisa
Olschewski,
Henrike
Hanssen,
Alexander
Münchau,
Andreas
Ferbert,
Norbert
Brüggemann, and
Katja
Lohmann,
De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient, Parkinsonism Relat Disord , vol. 64, pp. 337–339, 2019.
De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient, Parkinsonism Relat Disord , vol. 64, pp. 337–339, 2019.
DOI: | 10.1016/j.parkreldis.2019.03.018 |
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.
[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 |
Alexander Münchau,
Einige Leute simulieren Tourette nur, Frankfurter Allgemeine Sonntagszeitung , 2019.
Einige Leute simulieren Tourette nur, Frankfurter Allgemeine Sonntagszeitung , 2019.
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.
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 |