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There are 6409 results for: content related to: Spinocerebellar ataxias type 1, 2 and 3: a study of heart rate variability

  1. Coenzyme Q10 and spinocerebellar ataxias

    Movement Disorders

    Volume 30, Issue 2, February 2015, Pages: 214–220, Raymond Y. Lo, Karla P. Figueroa, Stefan M. Pulst, Chi-Ying Lin, Susan Perlman, George Wilmot, Christopher Gomez, Jeremy Schmahmann, Henry Paulson, Vikram G. Shakkottai, Sarah Ying, Theresa Zesiewicz, Khalaf Bushara, Michael Geschwind, Guangbin Xia, S.H. Subramony, Tetsuo Ashizawa and Sheng-Han Kuo

    Version of Record online : 1 DEC 2014, DOI: 10.1002/mds.26088

  2. 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

  3. Progressive impairment of cerebellar mGluR signalling and its therapeutic potential for cerebellar ataxia in spinocerebellar ataxia type 1 model mice

    The Journal of Physiology

    Anton N. Shuvaev, Nobutake Hosoi, Yamato Sato, Dai Yanagihara and Hirokazu Hirai

    Version of Record online : 15 SEP 2016, DOI: 10.1113/JP272950

  4. 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

  5. Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights

    Neuropathology and Applied Neurobiology

    Volume 38, Issue 7, December 2012, Pages: 665–680, U. Rüb, K. Bürk, D. Timmann, W. den Dunnen, K. Seidel, K. Farrag, E. Brunt, H. Heinsen, R. Egensperger, A. Bornemann, S. Schwarzacher, H.-W. Korf, L. Schöls, J. Bohl and T. Deller

    Version of Record online : 14 NOV 2012, DOI: 10.1111/j.1365-2990.2012.01259.x

  6. Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia

    American Journal of Medical Genetics

    Volume 95, Issue 4, 11 December 2000, Pages: 351–358, Elsdon Storey, Desiree du Sart, Janet H. Shaw, Peter Lorentzos, Louise Kelly, R.J. McKinley Gardner, Susan M. Forrest, Ivan Biros and Garth A. Nicholson

    Version of Record online : 5 DEC 2000, DOI: 10.1002/1096-8628(20001211)95:4<351::AID-AJMG10>3.0.CO;2-R

  7. 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

    Version of Record online : 2 MAR 2011, DOI: 10.1002/mds.23584

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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

  9. Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: Striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomography

    Movement Disorders

    Volume 21, Issue 10, October 2006, Pages: 1667–1673, Matthias Reimold, Christoph Globas, Marc Gleichmann, Michael Schulze, Christian Gerloff, Roland Bares, H.-J. Machulla and Katrin Bürk

    Version of Record online : 28 AUG 2006, DOI: 10.1002/mds.20978

  10. CAG repeats in restless legs syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 2, 5 March 2006, Pages: 173–176, Markus Konieczny, Peter Bauer, Jürgen Tomiuk, Gabriele Weisser, Jean Haan, Klaus Berger, Olaf Riess and Ludger Schöls

    Version of Record online : 2 JAN 2006, DOI: 10.1002/ajmg.b.30265

  11. Spinocerebellar ataxia: relationship between phenotype and genotype – a review

    Clinical Genetics

    Volume 90, Issue 4, October 2016, Pages: 305–314, Y.-M. Sun, C. Lu and Z.-Y. Wu

    Version of Record online : 30 JUN 2016, DOI: 10.1111/cge.12808

  12. You have full text access to this OnlineOpen article
    Survival and severity in dominant cerebellar ataxias

    Annals of Clinical and Translational Neurology

    Volume 2, Issue 2, February 2015, Pages: 202–207, Marie-Lorraine Monin, Sophie Tezenas du Montcel, Cecilia Marelli, Cecile Cazeneuve, Perrine Charles, Chantal Tallaksen, Sylvie Forlani, Giovanni Stevanin, Alexis Brice and Alexandra Durr

    Version of Record online : 7 JAN 2015, DOI: 10.1002/acn3.156

  13. The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population

    Acta Neurologica Scandinavica

    Volume 111, Issue 3, March 2005, Pages: 154–162, V. Juvonen, M. Hietala, V. Kairisto and M.-L. Savontaus

    Version of Record online : 27 JAN 2005, DOI: 10.1111/j.1600-0404.2005.00349.x

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    Dopamine D2 receptor signaling modulates mutant ataxin-1 S776 phosphorylation and aggregation

    Journal of Neurochemistry

    Volume 114, Issue 3, August 2010, Pages: 706–716, Scoty M. Hearst, Mariper E. Lopez, Qingmei Shao, Yong Liu and Parminder J. S. Vig

    Version of Record online : 30 APR 2010, DOI: 10.1111/j.1471-4159.2010.06791.x

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    Non-invasive detection of neurochemical changes prior to overt pathology in a mouse model of spinocerebellar ataxia type 1

    Journal of Neurochemistry

    Volume 127, Issue 5, December 2013, Pages: 660–668, Uzay E. Emir, Howard Brent Clark, Manda L. Vollmers, Lynn E. Eberly and Gülin Öz

    Version of Record online : 17 SEP 2013, DOI: 10.1111/jnc.12435

  16. A comparative study of cardiac dysautonomia in autosomal dominant spinocerebellar ataxias and idiopathic sporadic ataxias

    Acta Neurologica Scandinavica

    Volume 120, Issue 3, September 2009, Pages: 204–209, M. Netravathi, T. N. Sathyaprabha, K. Jayalaxmi, P. Datta, M. Nirmala and P. K. Pal

    Version of Record online : 28 JAN 2009, DOI: 10.1111/j.1600-0404.2008.01144.x

  17. Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan

    Acta Neurologica Scandinavica

    Volume 107, Issue 1, January 2003, Pages: 38–41, R. Matsumura, N. Futamura, N. Ando and S. Ueno

    Version of Record online : 14 JAN 2003, DOI: 10.1034/j.1600-0404.2003.01347.x

  18. Mesenchymal stem cells attenuate peripheral neuronal degeneration in spinocerebellar ataxia type 1 knockin mice

    Journal of Neuroscience Research

    Volume 94, Issue 3, March 2016, Pages: 246–252, Tokue Mieda, Nana Suto, Akira Iizuka, Serina Matsuura, Haku Iizuka, Kenji Takagishi, Kazuhiro Nakamura and Hirokazu Hirai

    Version of Record online : 28 DEC 2015, DOI: 10.1002/jnr.23698

  19. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

    Clinical Genetics

    Volume 65, Issue 3, March 2004, Pages: 209–214, YR Wu, HY Lin, CM Chen, K Gwinn-Hardy, LS Ro, YC Wang, SH Li, JC Hwang, K Fang, HM Hsieh-Li, ML Li, LC Tung, MT Su, KT Lu and GJ Lee-Chen

    Version of Record online : 30 JAN 2004, DOI: 10.1111/j.0009-9163.2004.00213.x

  20. Subclinical pulmonary dysfunction in spinocerebellar ataxias 1, 2 and 3

    Acta Neurologica Scandinavica

    Volume 122, Issue 5, November 2010, Pages: 323–328, S. J. Sriranjini, P. K. Pal, N. Krishna and T. N. Sathyaprabha

    Version of Record online : 30 NOV 2009, DOI: 10.1111/j.1600-0404.2009.01306.x