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There are 236277 results for: content related to: Self-rated health status in spinocerebellar ataxia—Results from a European multicenter study

  1. You have free access to this content
    Poster Presentations

    Movement Disorders

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

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25051

  2. Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

    Annals of Neurology

    Volume 42, Issue 6, December 1997, Pages: 924–932, Dr. Ludger Schöls, Georgios Amoiridis, Thomas Büttner, Horst Przuntek, Jörg T. Epplen and Olaf Riess

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410420615

  3. You have free access to this content
    Poster Presentations

    Movement Disorders

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

    Article first published online : 6 JUN 2014, DOI: 10.1002/mds.25914

  4. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7

    Neuropathology and Applied Neurobiology

    Volume 32, Issue 6, December 2006, Pages: 635–649, U. Rüb, E. R. Brunt, E. Petrasch-Parwez, L. Schöls, D. Theegarten, G. Auburger, K. Seidel, C. Schultz, K. Gierga, H. Paulson, C. Van Broeckhoven, T. Deller and R. A. I. De Vos

    Article first published online : 8 AUG 2006, DOI: 10.1111/j.1365-2990.2006.00772.x

  5. Proton magnetic resonance spectroscopic imaging reveals differences in spinocerebellar ataxia types 2 and 6

    Journal of Magnetic Resonance Imaging

    Volume 13, Issue 4, April 2001, Pages: 553–559, S.M. Boesch, M. Schocke, K. Bürk, P. Hollosi, F. Fornai, F.T. Aichner, W. Poewe and S. Felber

    Article first published online : 21 MAR 2001, DOI: 10.1002/jmri.1078

  6. Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum

    Neuropathology

    Volume 32, Issue 6, December 2012, Pages: 595–603, Makoto Takahashi, Kinya Ishikawa, Nozomu Sato, Masato Obayashi, Yusuke Niimi, Taro Ishiguro, Mitsunori Yamada, Yasuko Toyoshima, Hitoshi Takahashi, Takeo Kato, Masaki Takao, Shigeo Murayama, Osamu Mori, Yoshinobu Eishi and Hidehiro Mizusawa

    Article first published online : 7 MAR 2012, DOI: 10.1111/j.1440-1789.2012.01302.x

  7. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: A study of 1,286 Japanese patients

    American Journal of Medical Genetics

    Volume 114, Issue 5, 8 July 2002, Pages: 578–583, Hirofumi Maruyama, Yuishin Izumi, Hiroyuki Morino, Masaya Oda, Hiromasa Toji, Shigenobu Nakamura and Hideshi Kawakami

    Article first published online : 31 MAY 2002, DOI: 10.1002/ajmg.10514

  8. CAG repeat expansions in patients with sporadic cerebellar ataxia

    Acta Neurologica Scandinavica

    Volume 98, Issue 1, July 1998, Pages: 55–59, N. Futamura, R. Matsumura, Y. Fujimoto, H. Horikawa, A. Suzumura and T. Takayanagi

    Article first published online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1998.tb07378.x

  9. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 portuguese ataxia families

    American Journal of Medical Genetics

    Volume 81, Issue 2, 28 March 1998, Pages: 134–138, I. Silveira, P. Coutinho, P. Maciel, C. Gaspar, S. Hayes, A. Dias, J. Guimarães, L. Loureiro, J. Sequeiros and G.A. Rouleau

    Article first published online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980328)81:2<134::AID-AJMG3>3.0.CO;2-W

  10. Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect

    Clinical Genetics

    Volume 85, Issue 2, February 2014, Pages: 159–165, J.J. Magaña, Y.S. Tapia-Guerrero, L. Velázquez-Pérez, C.M. Cerecedo-Zapata, M. Maldonado-Rodríguez, J.S. Jano-Ito, N. Leyva-García, R. González-Piña, E. Martínez-Cruz, O. Hernández-Hernández and B. Cisneros

    Article first published online : 11 MAR 2013, DOI: 10.1111/cge.12114

  11. Searching for modulating effects of SCA2, SCA6 and DRPLA CAG tracts on the Machado-Joseph disease (SCA3) phenotype

    Acta Neurologica Scandinavica

    Volume 107, Issue 3, March 2003, Pages: 211–214, L. Jardim, I. Silveira, M. L. Pereira, M. Do Céu Moreira, P. Mendonça, J. Sequeiros and R. Giugliani

    Article first published online : 4 MAR 2003, DOI: 10.1034/j.1600-0404.2003.00046.x

  12. Age at onset variance analysis in spinocerebellar ataxias: A study in a Dutch–French cohort

    Annals of Neurology

    Volume 57, Issue 4, April 2005, Pages: 505–512, Bart P. C. van de Warrenburg, Harrie Hendriks, Alexandra Dürr, Martin C. A. van Zuijlen, Giovanni Stevanin, Agnès Camuzat, Richard J. Sinke, Alexis Brice and Berry P. H. Kremer

    Article first published online : 3 MAR 2005, DOI: 10.1002/ana.20424

  13. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6

    Clinical Genetics

    Volume 53, Issue 1, January 1998, Pages: 13–19, Hidetaka Watanabe, Fumiaki Tanaka, Michiyo Matsumoto, Manabu Doyu, Tetsuo Ando, Terunori Mitsuma and Gen Sobue

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1998.tb02575.x

  14. Ocular motor characteristics of different subtypes of spinocerebellar ataxia: Distinguishing features

    Movement Disorders

    Volume 28, Issue 9, August 2013, Pages: 1271–1277, Ji Sun Kim, Ji Soo Kim, Jinyoung Youn, Dae-Won Seo, Yuri Jeong, Ji-Hoon Kang, Jeong Ho Park and Jin Whan Cho

    Article first published online : 22 APR 2013, DOI: 10.1002/mds.25464

  15. 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

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

  16. 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

    Article first published online : 14 JAN 2003, DOI: 10.1034/j.1600-0404.2003.01347.x

  17. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan

    Acta Neurologica Scandinavica

    Volume 109, Issue 5, May 2004, Pages: 355–360, H.-F. Tsai, C.-S. Liu, T.-M. Leu, F.-C. Wen, S.-J. Lin, C.-C. Liu, D.-K. Yang, C. Li and M. Hsieh

    Article first published online : 3 NOV 2003, DOI: 10.1046/j.1600-0404.2003.00229.x

  18. Autosomal dominant cerebellar ataxias: a systematic review of clinical features

    European Journal of Neurology

    Volume 21, Issue 4, April 2014, Pages: 607–615, M. Rossi, S. Perez-Lloret, L. Doldan, D. Cerquetti, J. Balej, P. Millar Vernetti, M. Hawkes, A. Cammarota and M. Merello

    Article first published online : 12 FEB 2014, DOI: 10.1111/ene.12350

  19. Spinocerebellar Ataxias

    Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders, Second Edition

    Hidehiro Mizusawa, H. Brent Clark, Arnulf H. Koeppen, Pages: 273–287, 2011

    Published Online : 21 SEP 2011, DOI: 10.1002/9781444341256.ch27

  20. 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

    Article first published online : 30 JAN 2004, DOI: 10.1111/j.0009-9163.2004.00213.x