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Prof. Dr.med. Susanne Schneider

schneider

Dept. of Neurology
Ludwig-Maximilians-University Munich, Klinikum Großhadern
Feodor-Lynen-Straße 19, 81377 Munich, Germany

Tel. ++ 49 89 4400-74828
Fax ++ 49 89 4400-74801
susanne.schneider(at)med.uni-muenchen.de

Publications

 

Klinische Schwerpunkte

 

1. Bewegungsstörungen

  • Parkinson, Dystonie, Tremor, Chorea, Tics, Myoclonus, paroxysmale Dyskinesien
  • vererbte / genetische Formen

2. Klinische Genetik, seltene Erkrankungen

 

Main Research Topics

 

1. Clinical, diagnostic, pathophysiological and therapeutic aspects of Movement Disorders

2. Genetic Aspects of Movement Disorders

3. Neurodegenerative Diseases

4. Syndromes of Neurodegeneration with Brain Iron Accumulation (NBIA-Syndromes)

5. Elektrophysiological abnormalities of Movement Disorders (transcranial magnetic stimulation, TMS)

 

Selected Literature

 

- Schneider SA, Alcalay RN. Neuropathology of Genetic Synucleinopathies with Parkinsonism - review of the literature. Mov Disord. 2017;32(11):1504-1523

- Klettner A, Richert E, Kuhlenbäumer G, Nölle B, Bhatia KP, Deuschl G, Roider J, Schneider SA. Alpha synuclein and crystallin expression in human lens in Parkinson's disease. Mov Disord. 2016 Apr;31(4):600-1

- Dusek P, Schneider SA, Aaseth J Iron chelation in the treatment of neurodegenerative diseases. J Trace Elem Med Biol. 2016;38:81-92

- Müller SH, Girard SL, Hopfner F, Merner ND, Bourassa CV, Lorenz D, Clark LN, Tittmann L, Soto-Ortolaza AI, Klebe S, Hallett M, Schneider SA, Hodgkinson CA, Lieb W, Wszolek ZK, Pendziwiat M, Lorenzo-Betancor O, Poewe W, Ortega-Cubero S, Seppi K, Rajput A, Hussl A, Rajput AH, Berg D, Dion PA, Wurster I, Shulman JM, Srulijes K, Haubenberger D, Pastor P, Vilariño-Güell C, Postuma RB, Bernard G, Ladwig KH, Dupré N, Jankovic J, Strauch K, Panisset M, Winkelmann J, Testa CM, Reischl E, Zeuner KE, Ross OA, Arzberger T, Chouinard S, Deuschl G, Louis ED, Kuhlenbäumer G, Rouleau GA. Genome-wide association study in essential tremor identifies three new loci. Brain. 2016;139(Pt 12):3163-3169

- Schneider SA, Boettner M, Alexoudi A, Zorenkova D, Deuschl G, Wedel T. Can we use peripheral tissue biopsies to diagnose Parkinson´s disease? A review of the literature. Eur J Neurol 2016;23:247-6

- Brändl B, Schneider SA, Loring JF, Hardy J, Müller FJ. Stem cell research and reprogramming: basic implications and future perspective for movement disorders. Mov Disord 2015;30:301-12

- Muthuraman M, Deuschl G, Anwar AR, Mideksa KG, von Helmolt F, Schneider SA. Essential and aging-related tremor: Differences of central control. Mov Disord. 2015;30:1673-80

- Kun-Rodrigues C, Ganos C, Guerreiro R, Schneider SA, Schulte C, Lesage S, Darwent L, Holmans P, Singleton A; International Parkinson's Disease Genomics Consortium (IPDGC), Bhatia K, Bras J. A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. Hum Mol Genet. 2015;24(23):6711-20

- Dusek P, Tovar-Martinez E, Istvan Madai V, Jech R, Sobesky J, Paul F, Niendorf T, Wuerfel J, Schneider SA. Seven Tesla MRI for brain iron quantification in homozygous and heterozygous PANK2 mutation carriers. MDCP 12/2014; 1(4)

- Bras J, Guerreiro RJ, Teo JH, Darwent L, Vaughan J, Molloy S, Hardy J, Schneider SA. Atypical parkinsonism-dystonia syndrome caused by a novel DJ1 mutation. Mov Disord Clin Pract, 1/2014; 1(1)

- Schneider SA, Pleger B, Draganski B, Cordivari C, Rothwell JC, Bhatia KP, Dolan RJ. Modulatory effects of 5Hz rTMS over the primary somatosensory cortex in focal dystonia - an fMRI-TMS study. MovDisord 2010;25:76-83

- Djarmati A*, Schneider SA*, Lohmann K, Winkler S, Pawlack H, Hagenah J, Brüggemann N, Zittel S, Fuchs T, Raković A, Schmidt A, Jabusch HC, Wilcox R, Kostić VS, Siebner H, Altenmüller E, Münchau A, Ozelius LJ, Klein C. Mutations in the THAP1 (DYT6) and generalized dystonia with prominent spasmodic dysphonia: a genetic screening study. Lancet Neurol. 2009;8:447-52

- Paisan-Ruiz C, Bhatia KP, Li A, Hernandez D, Davis M, Wood NW, Hardy J, Houlden H, Singleton A, Schneider SA. Characterisation of PLA2G6 as a locus for dystonia-parkinsonism. Ann Neurol. 2009;65:19-23

- Schneider SA, Bhatia KP, Hardy J. Complicated recessive dystonia parkinsonism syndromes. MovDisord. 2009;24:490-9

- Schneider SA, Talelli P, Cheeran B, Khan N, Wood NW, Rothwell J, Bhatia KP. Corticospinal and intracortical excitability in patients and asymptomatic carriers with parkin gene mutations: a TMS study. MovDisord. 2008;23:1812-9

- Weber YG, Storch A, Wuttke TV, Brockmann K, Kempfle J, Maljevic S, Margari L, Kamm C, Schneider SA, Huber SM, Pekrun A, Roebling R, Seebohm G, Koka S, Lang C, Kraft E, Blazevic D, Salvo-Vargas A, Fauler M, Mottaghy FM, Münchau A, Edwards MJ, Presicci A, Margari F, Gasser T, Lang F, Bhatia KP, Lehmann-Horn F, Lerche H. Paroxysmal exertion-induced dyskinesias are caused by mutations in GLUT1 and an associated hemolytic anemia is linked to a cation leak of this glucose transporter. J Clin Invest. 2008;118:2157-68

- Schneider SA, van de Warrenburg BP, Hughes T, Davis M, Sweeney M, Wood N, Quinn NP, Bhatia KP. Phenotypic homogeneity of the Huntington’s disease-like presentation in a SCA17 family. Neurology. 2007;67:1701-3

Books:

- Donaldson C, Marsden CD, Schneider SA, Bhatia KP. Marsden’s Book of Movement Disorders. Oxford University Press. 2015. ISBN13: 9780192619112ISBN10: 019261911X Hardback, 1552 pages

- Schneider SA, Bras J. Movement Disorder Genetics. Eds: Schneider SA, Bras J. Springer, 2015. ISBN 978-3-319-17223-1

- Schneider SA, Bhatia KP. Metal Related Neurodegenerative Disease, International Review of Neurobiology, Vol. 110, Elsevier 2013

 

Methods

 

1) Klinische Genetik

2) Phänotyp-Genotyp-Korrelation

3) Radiologische Charakterisierung

4) Elektrophysiologie (Transkranielle Magnetstimulation /TMS)

 

Grants

 

Eugene Brehm Bequest, UCL London (2005)

JJ Astor Prize, Brain Research Trust, UK (2005-2008)

Intramurale Förderung durch die Universität zu Lübeck (2008-2010)

Graduierten-Stipendium der Novartis-Stiftung (2008) Eugene

Initiativgruppe „Neurobiomedizinische Forschung“ der Medizinischen Fakultäten der Universität zu Lübeck und der Christian-Albrechts-Universität zu Kiel (2010-2012)

Fast-Track-Stipendium der Robert-Bosch-Stiftung (2012-2013)

Intramurale Förderung der Universität Kiel (2013)

SFB 855 der Deutschen Forschungsgemeinschaft (DFG) (2012/2013)

Else Kröner-Fresenius-Stiftung (seit 2013)

Eva Luise und Horst Köhler Stiftung für seltene Erkrankungen (seit 2012)

Intramurale Förderung der LMU München (seit 2016)

Braun-Stiftung Melsungen (seit 2017)

 

Scientific Awards

 

Eugen Rehfisch-Preis (2018)

Leadership-Programm der International Movement Disorders Society (MDS-LEAP) (2014-2016)

Buch des Jahres – ausgezeichnet mit dem BMA Book Award 2013 für Marsden’s Book of Movement Dsorders. "This is the greatest, most authoritative and up-to-date book on movement disorders ever produced.. ... it is highly accessible, complete and reflects the thinking processes of neurologists engaged in clinical work. It is a marvel and may be wholly and unreservedly recommended" (2013)

Jon Stolk Award in Movement Disorders for Young Investigators, American Academy of Neurology (2011)

“Best Poster”-Preis, International Dystonia Society Meeting, Barcelona(2011)

Empiris-Award, Empiris-Foundation, Zurich (2010)

Oppenheim-Preis der Deutschen Dystonie Gesellschaft (2010)

Forschungspreis Pro ZNS - Dr. med. Joachim Elbrächter (2010)

David Marsden Award, European Dystonia Society (seit 2009)

Graduierten-Stipendum der Novartis-Stiftung (2008)

“Best Poster”-Award, ABN/IAN Joint Annual Meeting in Mumbai, Indien (2007)

“William Koller Memorial Fund Award for outstanding and innovative clinical research in the field of Movement Disorders”, Movement Disorders Society, Jahrestagung Kyoto, Japan (2006)

 

Team Members

 

n.n.

 

Cooperation with

 

Queen Square Institute of Neurology, England

Abt. für Neurologie, Universität Kiel

Max-Dellbrück Centrum (MDC) Charite Berlin

Abt. für Neurologie, Universität Prag

 
 

Anschrift

Neurologische Klinik und Poliklinik & Deutsches Schwindel- und Gleichgewichtszentrum DSGZ
Ludwig-Maximilians-Universität München, Klinikum Großhadern, Marchioninistraße 15
D-81377 München

Direktorin:
Univ.Prof. Dr. med. Marianne Dieterich, FANA, FEAN
direktion.neurologie
(at)med.uni-muenchen.de

Telefonzentrale
Tel. (089) 4400-0