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There are 24301 results for: content related to: Commentary

  1. You have free access to this content
    Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3-deficient heterozygous mice

    The Journal of Physiology

    Volume 591, Issue 13, July 2013, Pages: 3433–3449, Keiko Ikeda, Shin’Ichiro Satake, Tatsushi Onaka, Hiroki Sugimoto, Naoki Takeda, Keiji Imoto and Kiyoshi Kawakami

    Version of Record online : 4 JUN 2013, DOI: 10.1113/jphysiol.2012.247817

  2. Cognitive impairment in rapid-onset dystonia-parkinsonism

    Movement Disorders

    Volume 29, Issue 3, March 2014, Pages: 344–350, Jared F. Cook, Deborah F. Hill, Beverly M. Snively, Niki Boggs, Cynthia K. Suerken, Ihtsham Haq, Mark Stacy, W. Vaughn McCall, Laurie J. Ozelius, Kathleen J. Sweadner and Allison Brashear

    Version of Record online : 16 JAN 2014, DOI: 10.1002/mds.25790

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    Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly

    Epilepsia

    Volume 56, Issue 3, March 2015, Pages: 422–430, Alex R. Paciorkowski, Sharon S. McDaniel, Laura A. Jansen, Hannah Tully, Emily Tuttle, Dalia H. Ghoneim, Srinivasan Tupal, Sonya A. Gunter, Valeria Vasta, Qing Zhang, Thao Tran, Yi B. Liu, Laurie J. Ozelius, Allison Brashear, Kathleen J. Sweadner, William B. Dobyns and Sihoun Hahn

    Version of Record online : 5 FEB 2015, DOI: 10.1111/epi.12914

  4. The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms

    Movement Disorders

    Volume 30, Issue 6, May 2015, Pages: 770–779, Jin-Sung Park, Nicholas F. Blair and Carolyn M. Sue

    Version of Record online : 21 APR 2015, DOI: 10.1002/mds.26243

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    ATP1A3 mutations in infants: a new rapid-onset dystonia–Parkinsonism phenotype characterized by motor delay and ataxia

    Developmental Medicine & Child Neurology

    Volume 54, Issue 11, November 2012, Pages: 1065–1067, ALLISON BRASHEAR, JONATHAN W MINK, DEBORAH F HILL, NIKI BOGGS, W VAUGHN MCCALL, MARK A STACY, BEVERLY SNIVELY, LANEY S LIGHT, KATHLEEN J SWEADNER, LAURIE J OZELIUS and LESLIE MORRISON

    Version of Record online : 28 AUG 2012, DOI: 10.1111/j.1469-8749.2012.04421.x

  6. Engineering animal models of dystonia

    Movement Disorders

    Volume 28, Issue 7, 15 June 2013, Pages: 990–1000, Janneth Oleas, Fumiaki Yokoi, Mark P. DeAndrade, Antonio Pisani and Yuqing Li

    Version of Record online : 25 JUL 2013, DOI: 10.1002/mds.25583

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    Knock-in mouse model of alternating hemiplegia of childhood: Behavioral and electrophysiologic characterization

    Epilepsia

    Volume 56, Issue 1, January 2015, Pages: 82–93, Arsen S. Hunanyan, Nina A. Fainberg, Molly Linabarger, Eric Arehart, A. Soren Leonard, Syed M. Adil, Ashley R. Helseth, Amanda K. Swearingen, Stacy L. Forbes, Ramona M. Rodriguiz, Theodore Rhodes, Xiaodi Yao, Nadine Kibbi, Daryl W. Hochman, William C. Wetsel, Ute Hochgeschwender and Mohamad A. Mikati

    Version of Record online : 19 DEC 2014, DOI: 10.1111/epi.12878

  8. Rapid-Onset Dystonia-Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation

    Movement Disorders Clinical Practice

    Volume 2, Issue 1, March 2015, Pages: 74–75, Ai Huey Tan, Laurie J. Ozelius, Allison Brashear, Anthony E. Lang, Azlina Ahmad-Annuar, Chong Tin Tan and Shen-Yang Lim

    Version of Record online : 30 DEC 2014, DOI: 10.1002/mdc3.12122

  9. 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

  10. Endolysosomal dysfunction in Parkinson's disease: Recent developments and future challenges

    Movement Disorders

    Volume 31, Issue 10, October 2016, Pages: 1433–1443, Lauren R. Kett and William T. Dauer

    Version of Record online : 13 SEP 2016, DOI: 10.1002/mds.26797

  11. Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia–parkinsonism

    Movement Disorders

    Volume 29, Issue 1, January 2014, Pages: 153–154, Masayuki Sasaki, Atsushi Ishii, Yoshiaki Saito and Shinichi Hirose

    Version of Record online : 30 SEP 2013, DOI: 10.1002/mds.25659

  12. 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

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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

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    Decreased neuronal Na+,K+-ATPase activity in Atp1a3 heterozygous mice increases susceptibility to depression-like endophenotypes by chronic variable stress

    Genes, Brain and Behavior

    Volume 10, Issue 5, July 2011, Pages: 542–550, G. S. Kirshenbaum, K. Saltzman, B. Rose, J. Petersen, B. Vilsen and J. C. Roder

    Version of Record online : 13 APR 2011, DOI: 10.1111/j.1601-183X.2011.00691.x

  15. The multiple faces of the ATP1A3-related dystonic movement disorder

    Movement Disorders

    Volume 28, Issue 10, September 2013, Pages: 1457–1459, Anne Roubergue, Emmanuel Roze, Sandrine Vuillaumier-Barrot, Marie-Joséphine Fontenille, Aurélie Méneret, Marie Vidailhet, Bertrand Fontaine, Diane Doummar, Bertrand Philibert, Florence Riant and Sophie Nicole

    Version of Record online : 8 MAR 2013, DOI: 10.1002/mds.25396

  16. Milestones in dystonia

    Movement Disorders

    Volume 26, Issue 6, May 2011, Pages: 1106–1126, Laurie J. Ozelius, Naomi Lubarr and Susan B. Bressman

    Version of Record online : 27 MAY 2011, DOI: 10.1002/mds.23775

  17. 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

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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

  19. 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

  20. 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