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There are 14191 results for: content related to: Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patients

  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. Childhood-onset ataxia: Testing for large CAG-repeats in SCA2 and SCA7

    American Journal of Medical Genetics

    Volume 110, Issue 4, 15 July 2002, Pages: 338–345, Rong Mao, Arthur S. Aylsworth, Nicholas Potter, William G. Wilson, Galen Breningstall, Myra J. Wick, Dusica Babovic-Vuksanovic, Martha Nance, Marc C. Patterson, Christopher M. Gomez and Karen Snow

    Article first published online : 9 MAY 2002, DOI: 10.1002/ajmg.10467

  3. You have free access to this content
    Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings

    Movement Disorders

    Volume 24, Issue 13, 15 October 2009, Pages: 2007–2011, Jun-Ling Wang, Bin Xiao, Xiang-Xiang Cui, Ji-Feng Guo, Li-Fang Lei, Xing-Wang Song, Lu Shen, Hong Jiang, Xin-Xiang Yan, Qian Pan, Zhi-Gao Long, Kun Xia and Bei-Sha Tang

    Article first published online : 11 AUG 2009, DOI: 10.1002/mds.22727

  4. SCA2 may present as levodopa-responsive parkinsonism

    Movement Disorders

    Volume 18, Issue 4, April 2003, Pages: 425–429, Haydeh Payami, John Nutt, Steven Gancher, Thomas Bird, Melissa Gonzales McNeal, William K. Seltzer, Jennifer Hussey, Paul Lockhart, Katrina Gwinn-Hardy, Amanda A. Singleton, Andrew B. Singleton, John Hardy and Matthew Farrer

    Article first published online : 20 DEC 2002, DOI: 10.1002/mds.10375

  5. Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2)

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 2, March 2010, Pages: 524–531, Eliana Marisa Ramos, Sandra Martins, Isabel Alonso, Vanessa E. Emmel, Maria Luiza Saraiva-Pereira, Laura Bannach Jardim, Paula Coutinho, Jorge Sequeiros and Isabel Silveira

    Article first published online : 12 AUG 2009, DOI: 10.1002/ajmg.b.31013

  6. Brisk deep-tendon reflexes as a distinctive phenotype in an argentinean spinocerebellar ataxia type 2 pedigree

    Movement Disorders

    Volume 21, Issue 1, January 2006, Pages: 66–68, Alberto L. Rosa, Irma Molina, Valeria Kowaljow and Cecilia B. Conde

    Article first published online : 17 AUG 2005, DOI: 10.1002/mds.20636

  7. Cortical atrophy in the cerebellar variant of multiple system atrophy: A voxel-based morphometry study

    Movement Disorders

    Volume 21, Issue 2, February 2006, Pages: 159–165, Christian Brenneis, Sylvia M. Boesch, Karl E. Egger, Klaus Seppi, Christoph Scherfler, Michael Schocke, Gregor K. Wenning and Werner Poewe

    Article first published online : 13 SEP 2005, DOI: 10.1002/mds.20656

  8. 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

  9. Spinocerebellar ataxia type 2 with levodopa-responsive parkinsonism culminating in motor neuron disease

    Movement Disorders

    Volume 19, Issue 7, July 2004, Pages: 848–852, Jon Infante, José Berciano, Victor Volpini, Jordi Corral, José Miguel Polo, Julio Pascual and Onofre Combarros

    Article first published online : 17 MAR 2004, DOI: 10.1002/mds.20090

  10. 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

  11. Abnormalities of dopaminergic neurotransmission in SCA2: A combined 123I-βCIT and 123I-IBZM SPECT study

    Movement Disorders

    Volume 19, Issue 11, November 2004, Pages: 1320–1325, Sylvia M. Boesch, Eveline Donnemiller, Jörg Müller, Klaus Seppi, Helga Weirich-Schwaiger, Werner Poewe and Gregor K. Wenning

    Article first published online : 26 MAY 2004, DOI: 10.1002/mds.20159

  12. Identification of five Spinocerebellar Ataxia Type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan

    Acta Neurologica Scandinavica

    Volume 100, Issue 3, September 1999, Pages: 189–194, M. Hsieh, S.-Y. Li, C.-J. Tsai, Y.-Y. Chen, C.-S. Liu, C.-Y. Chan, L.-S. Ro, D.-F. Chen, S.-S. Chen and C. Li

    Article first published online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1999.tb00737.x

  13. Clinical Aspects of CAG Repeat Diseases

    Brain Pathology

    Volume 7, Issue 3, July 1997, Pages: 881–900, Martha A. Nance

    Article first published online : 28 JAN 2008, DOI: 10.1111/j.1750-3639.1997.tb00892.x

  14. 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

  15. 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

  16. Phenotype variability in spinocerebellar ataxia type 2: A longitudinal family survey and a case featuring an unusual benign course of disease

    Movement Disorders

    Volume 24, Issue 5, 15 April 2009, Pages: 774–777, Sascha Hering, Clemens Achmüller, Andrea Köhler, Werner Poewe, Raine Schneider and Sylvia M. Boesch

    Article first published online : 17 FEB 2009, DOI: 10.1002/mds.22465

  17. SCA8 in the Spanish population including one homozygous patient

    Clinical Genetics

    Volume 62, Issue 5, November 2002, Pages: 404–409, B Tazón, C Badenas, L Jiménez, E Muñoz and M Milà

    Article first published online : 11 NOV 2002, DOI: 10.1034/j.1399-0004.2002.620509.x

  18. Large normal alleles and SCA2 prevalence: lessons from a nationwide study and analysis of the literature

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 96–98, J.M. Laffita-Mesa, L.E. Almaguer-Mederos, V. Kourí, P.O. Bauer, Y. Vázquez-Mojena, T. Cruz Mariño and L. Velázquez-Pérez

    Article first published online : 18 JUL 2013, DOI: 10.1111/cge.12221

  19. Brain structural damage in spinocerebellar ataxia type 2. A voxel-based morphometry study

    Movement Disorders

    Volume 23, Issue 6, 30 April 2008, Pages: 899–903, Riccardo Della Nave, Andrea Ginestroni, Carlo Tessa, Mirco Cosottini, Marco Giannelli, Elena Salvatore, Ferdinando Sartucci, Giuseppe De Michele, Maria Teresa Dotti, Silvia Piacentini and Mario Mascalchi

    Article first published online : 29 FEB 2008, DOI: 10.1002/mds.21982

  20. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population

    Movement Disorders

    Volume 22, Issue 7, 15 May 2007, Pages: 1050–1053, Elisa Alonso, Leticia Martínez-Ruano, Irene De Biase, Christopher Mader, Adriana Ochoa, Petra Yescas, Roxana Gutiérrez, Misti White, Luís Ruano, Marcela Fragoso-Benítez, Tetsuo Ashizawa, Sanjay I. Bidichandani and Astrid Rasmussen

    Article first published online : 11 APR 2007, DOI: 10.1002/mds.21470