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There are 9957 results for: content related to: Rare autosomal dominant mutations in GNAL are associated with primary torsion dystonia

  1. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  2. Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites

    Movement Disorders

    Volume 29, Issue 6, May 2014, Pages: 812–818, Rachel Saunders-Pullman, Tania Fuchs, Marta San Luciano, Deborah Raymond, Alison Brashear, Robert Ortega, Andres Deik, Laurie J. Ozelius and Susan B. Bressman

    Version of Record online : 5 FEB 2014, DOI: 10.1002/mds.25818

  3. You have free access to this content
    Poster Presentations

    Movement Disorders

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

    Version of Record online : 6 JUN 2014, DOI: 10.1002/mds.25914

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    Isolated and combined dystonia syndromes – an update on new genes and their phenotypes

    European Journal of Neurology

    Volume 22, Issue 4, April 2015, Pages: 610–617, B. Balint and K. P. Bhatia

    Version of Record online : 29 JAN 2015, DOI: 10.1111/ene.12650

  5. Novel GNAL mutations in two German patients with sporadic dystonia

    Movement Disorders

    Volume 29, Issue 14, December 2014, Pages: 1833–1834, Julia Ziegan, Matthias Wittstock, Ana Westenberger, Valerija Dobričić, Alexander Wolters, Reiner Benecke, Christine Klein and Christoph Kamm

    Version of Record online : 7 NOV 2014, DOI: 10.1002/mds.26066

  6. Genetics of dystonia: What's known? What's new? What's next?

    Movement Disorders

    Volume 28, Issue 7, 15 June 2013, Pages: 899–905, Katja Lohmann and Christine Klein

    Version of Record online : 25 JUL 2013, DOI: 10.1002/mds.25536

  7. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

    Movement Disorders

    Volume 29, Issue 1, January 2014, Pages: 143–147, Michael Zech, Nadine Gross, Angela Jochim, Florian Castrop, Maria Kaffe, Christian Dresel, Peter Lichtner, Annette Peters, Christian Gieger, Thomas Meitinger, Bernhard Haslinger and Juliane Winkelmann

    Version of Record online : 22 OCT 2013, DOI: 10.1002/mds.25715

  8. Screening of mutations in GNAL in sporadic dystonia patients

    Movement Disorders

    Volume 29, Issue 9, August 2014, Pages: 1193–1196, Claudia Dufke, Marc Sturm, Christopher Schroeder, Susanne Moll, Thomas Ott, Olaf Riess, Peter Bauer and Kathrin Grundmann

    Version of Record online : 9 JAN 2014, DOI: 10.1002/mds.25794

  9. The focal dystonias: Current views and challenges for future research

    Movement Disorders

    Volume 28, Issue 7, 15 June 2013, Pages: 926–943, H. A. Jinnah, Alfredo Berardelli, Cynthia Comella, Giovanni DeFazio, Mahlon R. DeLong, Stewart Factor, Wendy R. Galpern, Mark Hallett, Christy L. Ludlow, Joel S. Perlmutter, Ami R. Rosen and for the Dystonia Coalition Investigators

    Version of Record online : 25 JUL 2013, DOI: 10.1002/mds.25567

  10. Novel genes and novel pathogenetic mechanisms in adult-onset primary dystonia

    Movement Disorders

    Volume 28, Issue 4, April 2013, Page: 440, Simona Petrucci and Enza Maria Valente

    Version of Record online : 8 APR 2013, DOI: 10.1002/mds.25412

  11. Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families

    Movement Disorders

    Volume 30, Issue 5, 15 April 2015, Pages: 743–744, Ling-Yan Ma, Lin Wang, Ying-Mai Yang, Tao Feng and Xin-Hua Wan

    Version of Record online : 4 APR 2015, DOI: 10.1002/mds.26190

  12. GNAL mutation in isolated laryngeal dystonia

    Movement Disorders

    Volume 31, Issue 5, May 2016, Pages: 750–755, Gregory G. Putzel, Tania Fuchs, Giovanni Battistella, Estee Rubien-Thomas, Steven J. Frucht, Andrew Blitzer, Laurie J. Ozelius and Kristina Simonyan

    Version of Record online : 1 FEB 2016, DOI: 10.1002/mds.26502

  13. Emerging common molecular pathways for primary dystonia

    Movement Disorders

    Volume 28, Issue 7, 15 June 2013, Pages: 968–981, Mark S. LeDoux, William T. Dauer and Thomas T. Warner

    Version of Record online : 25 JUL 2013, DOI: 10.1002/mds.25547

  14. Primary dystonia: Moribund or viable

    Movement Disorders

    Volume 28, Issue 7, 15 June 2013, Pages: 906–913, Susan B. Bressman and Rachel Saunders-Pullman

    Version of Record online : 25 JUL 2013, DOI: 10.1002/mds.25528

  15. CK2 in Embryonic Development

    Protein Kinase CK2

    Laura Macias Alvarez, Jesus Revuelta-Cervantes, Isabel Dominguez, Pages: 129–168, 2013

    Published Online : 5 MAR 2013, DOI: 10.1002/9781118482490.ch4

  16. A comparison of molecular alterations in environmental and genetic rat models of ADHD: A pilot study

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 8, 5 December 2008, Pages: 1554–1563, Tania DasBanerjee, Frank A. Middleton, David F. Berger, John P. Lombardo, Terje Sagvolden and Stephen V. Faraone

    Version of Record online : 20 OCT 2008, DOI: 10.1002/ajmg.b.30877

  17. TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia

    Movement Disorders

    Volume 30, Issue 13, November 2015, Pages: 1853–1854, Michael Zech, Sylvia Boesch, Thomas Sycha, Joerg Mueller, Werner Poewe and Juliane Winkelmann

    Version of Record online : 28 OCT 2015, DOI: 10.1002/mds.26458

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    List of Abstracts

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S568–S633,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26296

  19. De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient

    Movement Disorders

    Volume 29, Issue 9, August 2014, Pages: 1190–1193, Valerija Dobričić, Nikola Kresojević, Ana Westenberger, Marina Svetel, Aleksandra Tomić, Vesna Ralić, Igor Petrović, Milica Ječmenica Lukić, Katja Lohmann, Ivana Novaković, Christine Klein and Vladimir S. Kostić

    Version of Record online : 13 APR 2014, DOI: 10.1002/mds.25876

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    Poster Session

    Movement Disorders

    Volume 31, Issue S2, June 2016, Pages: S1–S697,

    Version of Record online : 19 JUN 2016, DOI: 10.1002/mds.26688