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There are 65245 results for: content related to: Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism

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    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25051

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    Poster Presentations

    Movement Disorders

    Volume 29, Issue S1, May 2014, Pages: S1–S571,

    Article first published online : 6 JUN 2014, DOI: 10.1002/mds.25914

  3. Abstracts of The Movement Disorder Society's Twelfth International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 23, Issue S1, 15 May 2008, Pages: S1–S422,

    Article first published online : 28 MAY 2008, DOI: 10.1002/mds.22133

  4. Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 4, 5 June 2007, Pages: 434–438, Chin-Hsien Lin, Wuh-Liang Hwu, Shu-Chuan Chiang, Chun-Hwei Tai and Ruey-Meei Wu

    Article first published online : 17 APR 2007, DOI: 10.1002/ajmg.b.30427

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    Abstracts of The Movement Disorder Society's Eleventh International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 22, Issue S16, 2007, Pages: S1–S325,

    Article first published online : 24 APR 2007, DOI: 10.1002/mds.21535

  6. Movement disorders in spinocerebellar ataxias

    Movement Disorders

    Volume 26, Issue 5, April 2011, Pages: 792–800, Judith van Gaalen, Paola Giunti and Bart P. van de Warrenburg

    Article first published online : 2 MAR 2011, DOI: 10.1002/mds.23584

  7. International meeting on atypical parkinsonian disorders, Innsbruck, Austria, 19–21 February 2003

    Movement Disorders

    Volume 20, Issue S12, August 2005, Pages: S127–S148,

    Article first published online : 9 AUG 2005, DOI: 10.1002/mds.20620

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    List of Abstracts

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S524–S592,

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25052

  9. Hereditary parkinsonism: Parkinson disease look-alikes—An algorithm for clinicians to “PARK” genes and beyond

    Movement Disorders

    Volume 24, Issue 14, 30 October 2009, Pages: 2042–2058, Christine Klein, Susanne A. Schneider and Anthony E. Lang

    Article first published online : 4 SEP 2009, DOI: 10.1002/mds.22675

  10. “Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy—A diagnostic guide

    Movement Disorders

    Volume 28, Issue 9, August 2013, Pages: 1184–1199, Maria Stamelou, Niall P. Quinn and Kailash P. Bhatia

    Article first published online : 29 MAY 2013, DOI: 10.1002/mds.25509

  11. Poster Session 2, Monday 10 September

    European Journal of Neurology

    Volume 19, Issue s1, September 2012, Pages: 458–807,

    Article first published online : 7 SEP 2012, DOI: 10.1111/j.1468-1331.2012.03889.x

  12. Poster session 1: Sunday, March 6th, Poster numbers 1–187

    Movement Disorders

    Volume 20, Issue S10, February 2005, Pages: S1–S56,

    Article first published online : 9 FEB 2005, DOI: 10.1002/mds.20422

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    Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings

    Movement Disorders

    Volume 24, Issue 13, 15 October 2009, Pages: 2007–2011, Jun-Ling Wang, Bin Xiao, Xiang-Xiang Cui, Ji-Feng Guo, Li-Fang Lei, Xing-Wang Song, Lu Shen, Hong Jiang, Xin-Xiang Yan, Qian Pan, Zhi-Gao Long, Kun Xia and Bei-Sha Tang

    Article first published online : 11 AUG 2009, DOI: 10.1002/mds.22727

  14. Poster session 1, Abstracts 1–90

    Movement Disorders

    Volume 19, Issue S9, 2004, Pages: S19–S47,

    Article first published online : 10 MAY 2004, DOI: 10.1002/mds.20168

  15. 2nd World Parkinson Congress Abstracts

    Movement Disorders

    Volume 25, Issue S3, 15 September 2010, Pages: S569–S717,

    Article first published online : 9 SEP 2010, DOI: 10.1002/mds.23386

    Corrected by:

    Erratum: Erratum

    Vol. 25, Issue 15, 2694, Article first published online: 10 NOV 2010

  16. Poster Session 1

    Movement Disorders

    Volume 21, Issue S15, September 2006, Pages: S329–S424,

    Article first published online : 20 SEP 2006, DOI: 10.1002/mds.21246

  17. Autosomal dominant cerebellar ataxias: a systematic review of clinical features

    European Journal of Neurology

    Volume 21, Issue 4, April 2014, Pages: 607–615, M. Rossi, S. Perez-Lloret, L. Doldan, D. Cerquetti, J. Balej, P. Millar Vernetti, M. Hawkes, A. Cammarota and M. Merello

    Article first published online : 12 FEB 2014, DOI: 10.1111/ene.12350

  18. Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

    Annals of Neurology

    Volume 42, Issue 6, December 1997, Pages: 924–932, Dr. Ludger Schöls, Georgios Amoiridis, Thomas Büttner, Horst Przuntek, Jörg T. Epplen and Olaf Riess

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410420615

  19. Poster session 5: Nonmotor aspects of movement disorders, clinical, Parkinsonism

    Movement Disorders

    Volume 17, Issue S5, November 2002, Pages: S218–S263,

    Article first published online : 21 OCT 2002, DOI: 10.1002/mds.10353

  20. Poster session 4, Abstracts 1074–1130

    Movement Disorders

    Volume 19, Issue S9, 2004, Pages: S367–S386,

    Article first published online : 10 MAY 2004, DOI: 10.1002/mds.20181