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There are 21950 results for: content related to: Eye movement disorders in ATP13A2 mutation carriers (PARK9)

  1. 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

  2. You have free access to this content
    Poster Presentations

    Movement Disorders

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

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25051

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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

  4. Abstracts

    Movement Disorders

    Volume 29, Issue S2, November 2014, Pages: S13–S101,

    Version of Record online : 26 NOV 2014, DOI: 10.1002/mds.26090

  5. Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism

    Human Mutation

    Volume 32, Issue 8, August 2011, Pages: 956–964, Jin-Sung Park, Prachi Mehta, Antony A. Cooper, David Veivers, André Heimbach, Barbara Stiller, Christian Kubisch, Victor S. Fung, Dimitri Krainc, Alan Mackay-Sim and Carolyn M. Sue

    Version of Record online : 12 JUL 2011, DOI: 10.1002/humu.21527

  6. 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

  7. You have free access to this content
    Hypoxia regulation of ATP13A2 (PARK9) gene transcription

    Journal of Neurochemistry

    Volume 122, Issue 2, July 2012, Pages: 251–259, Qian Xu, Hongling Guo, Xiaojie Zhang, Beisha Tang, Fang Cai, Weihui Zhou and Weihong Song

    Version of Record online : 17 FEB 2012, DOI: 10.1111/j.1471-4159.2012.07676.x

  8. Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)

    Clinical Genetics

    Volume 82, Issue 3, September 2012, Pages: 256–263, H Eiberg, L Hansen, L Korbo, IM Nielsen, K Svenstrup, S Bech, LH Pinborg, L Friberg, LE Hjermind, OR Olsen and JE Nielsen

    Version of Record online : 18 JUL 2011, DOI: 10.1111/j.1399-0004.2011.01745.x

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    ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons

    FEBS Letters

    Volume 587, Issue 9, May 02, 2013, Pages: 1316–1325, Hideaki Matsui, Fumiaki Sato, Shigeto Sato, Masato Koike, Yosuke Taruno, Shinji Saiki, Manabu Funayama, Hidefumi Ito, Yoshihito Taniguchi, Norihito Uemura, Atsushi Toyoda, Yoshiyuki Sakaki, Shunichi Takeda, Yasuo Uchiyama, Nobutaka Hattori and Ryosuke Takahashi

    Version of Record online : 13 MAR 2013, DOI: 10.1016/j.febslet.2013.02.046

  10. Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants

    Journal of Neuroscience Research

    Volume 90, Issue 12, December 2012, Pages: 2306–2316, Jason P. Covy, Elisa A. Waxman and Benoit I. Giasson

    Version of Record online : 30 JUL 2012, DOI: 10.1002/jnr.23112

  11. Camptocormia and myopathy

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2689–2690, Günther Deuschl, Nils Margraf, Simone Spuler, Abdreas Kupsch and Walter J. Schulz-Schaeffer

    Version of Record online : 14 SEP 2010, DOI: 10.1002/mds.23363

  12. 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,

    Version of Record online : 28 MAY 2008, DOI: 10.1002/mds.22133

  13. Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations

    Movement Disorders

    Volume 27, Issue 1, January 2012, Pages: 42–53, Susanne A. Schneider, John Hardy and Kailash P. Bhatia

    Version of Record online : 26 OCT 2011, DOI: 10.1002/mds.23971

  14. PRICKLE1 progressive myoclonus epilepsy in Southern Italy

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2686–2687, C. Criscuolo, M.F. de Leva, P. Sorrentino, R. Piro, R. Carbone, A. Guacci, G. De Michele and A. Filla

    Version of Record online : 14 SEP 2010, DOI: 10.1002/mds.23350

  15. Reduced glutathione and Parkinson's disease

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2690–2691, Gian Pietro Sechi

    Version of Record online : 28 SEP 2010, DOI: 10.1002/mds.23383

  16. Dyskinesia–hyperpyrexia syndrome: Another Parkinson's disease emergency

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2691–2692, Silvia Gil-Navarro and Francisco Grandas

    Version of Record online : 18 AUG 2010, DOI: 10.1002/mds.23255

  17. Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations

    Movement Disorders

    Volume 25, Issue 12, 15 September 2010, Pages: 1929–1937, Maria I. Behrens, Norbert Brüggemann, Pedro Chana, Pablo Venegas, Marianne Kägi, Teresa Parrao, Patricia Orellana, Cristian Garrido, Cecilia V. Rojas, Jan Hauke, Eric Hahnen, Rafael González, Nicolas Seleme, Verónica Fernández, Alexander Schmidt, Ferdinand Binkofski, Detlef Kömpf, Christian Kubisch, Johann Hagenah, Christine Klein and Alfredo Ramirez

    Version of Record online : 3 AUG 2010, DOI: 10.1002/mds.22996

  18. Iatrogenic belly dancer syndrome following quadruple deep brain stimulation in a patient with myoclonus dystonia (DYT11)

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2692–2693, Elmar Lobsien, Doreen Gruber, Gerd-Helge Schneider, Andrea A. Kühn and Andreas Kupsch

    Version of Record online : 27 AUG 2010, DOI: 10.1002/mds.23276

  19. “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

    Version of Record online : 29 MAY 2013, DOI: 10.1002/mds.25509

  20. ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation

    Movement Disorders

    Volume 25, Issue 8, 15 June 2010, Pages: 979–984, Susanne A. Schneider, Coro Paisan-Ruiz, Niall P. Quinn, Andrew J. Lees, Henry Houlden, John Hardy and Kailash P. Bhatia

    Version of Record online : 22 MAR 2010, DOI: 10.1002/mds.22947