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There are 27888 results for: content related to: Screening of mutations in GNAL in sporadic dystonia patients

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  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. 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

  8. 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

  9. 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

  10. 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

  11. 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

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    No pathogenic GNAL mutations in 192 sporadic and familial cases of cervical dystonia

    Movement Disorders

    Volume 29, Issue 1, January 2014, Pages: 154–155, Gavin Charlesworth, Kailash P. Bhatia and Nicholas W. Wood

    Version of Record online : 12 NOV 2013, DOI: 10.1002/mds.25713

  13. 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

  14. Mutations in CIZ1 are not a major cause for dystonia in Germany

    Movement Disorders

    Volume 30, Issue 5, 15 April 2015, Pages: 740–743, Claudia Dufke, Ann-Kathrin Hauser, Marc Sturm, Susanne Fluhr, Tobias Wächter, Barbara Leube, Georg Auburger, Thomas Ott, Peter Bauer, Thomas Gasser and Kathrin Grundmann

    Version of Record online : 17 MAR 2015, DOI: 10.1002/mds.26198

  15. 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

  16. Therapeutic advances in dystonia

    Movement Disorders

    Volume 30, Issue 11, 15 September 2015, Pages: 1547–1556, Alberto Albanese, Luigi M. Romito and Daniela Calandrella

    Version of Record online : 24 AUG 2015, DOI: 10.1002/mds.26384

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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

  18. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

    Movement Disorders

    Volume 31, Issue 4, April 2016, Pages: 436–457, Connie Marras, Anthony Lang, Bart P. van de Warrenburg, Carolyn M. Sue, Sarah J. Tabrizi, Lars Bertram, Saadet Mercimek-Mahmutoglu, Darius Ebrahimi-Fakhari, Thomas T. Warner, Alexandra Durr, Birgit Assmann, Katja Lohmann, Vladimir Kostic and Christine Klein

    Version of Record online : 15 APR 2016, DOI: 10.1002/mds.26527

  19. Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up

    Movement Disorders

    Michael Zech, Sylvia Boesch, Angela Jochim, Sandrina Weber, Tobias Meindl, Barbara Schormair, Thomas Wieland, Christian Lunetta, Valeria Sansone, Michael Messner, Joerg Mueller, Andres Ceballos-Baumann, Tim M. Strom, Roberto Colombo, Werner Poewe, Bernhard Haslinger and Juliane Winkelmann

    Version of Record online : 26 SEP 2016, DOI: 10.1002/mds.26808

  20. Pisa syndrome in Parkinson's disease: An integrated approach from pathophysiology to management

    Movement Disorders

    Volume 31, Issue 12, December 2016, Pages: 1785–1795, Michele Tinazzi, Christian Geroin, Marialuisa Gandolfi, Nicola Smania, Stefano Tamburin, Francesca Morgante and Alfonso Fasano

    Version of Record online : 25 OCT 2016, DOI: 10.1002/mds.26829