1. The highly heterogeneous spinocerebellar ataxias: From genes to targets for therapeutic intervention

   • Antoni Matilla-Dueñas

   Introduction to the special issue 04 April 2008 Pages: 97 - 100

2. The clinical diagnosis of autosomal dominant spinocerebellar ataxias

   • Thomas Klockgether

   Original Article 12 April 2008 Pages: 101 - 105

3. Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1

   • Antoni Matilla-Dueñas
   • Robert Goold
   • Paola Giunti

   Original Article 03 April 2008 Pages: 106 - 114

4. Spinocerebellar ataxia 2 (SCA2)

   • Isabel Lastres-Becker
   • Udo Rüb
   • Georg Auburger

   Original Article 03 April 2008 Pages: 115 - 124

5. SCA3: Neurological features, pathogenesis and animal models

   • Olaf Riess
   • Udo Rüb
   • Ludger Schöls

   Original Article 26 March 2008 Pages: 125 - 137

6. Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration

   • Gwenn A. Garden
   • Albert R. La Spada

   OriginalPaper 12 April 2008 Pages: 138 - 149

7. Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes

   • Yoshio Ikeda
   • Randy S. Daughters
   • Laura P. W. Ranum

   Article 03 April 2008 Pages: 150 - 158

8. Clinical and genetic analysis of spinocerebellar ataxia type 11

   • Janel Johnson
   • Nicholas Wood
   • Henry Houlden

   Article 12 April 2008 Pages: 159 - 164

9. SCA13

   • M. F. Waters
   • S. M. Pulst

   OriginalPaper 01 July 2008 Pages: 165 - 169

   

10. Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4)

    • Giovanni Stevanin
    • Alexis Brice

    Original Article 26 March 2008 Pages: 170 - 178

11. Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21)

    • J. Delplanque
    • D. Devos
    • B. Sablonnière

    Original Article 26 March 2008 Pages: 179 - 183

12. Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis

    • Caterina Mariotti
    • Alfredo Brusco
    • Franco Taroni

    Original Article 04 September 2008 Pages: 184 - 188

13. Sporadic ataxias in Japan – a population-based epidemiological study

    • Shoji Tsuji
    • Osamu Onodera
    • On Behalf of the Study Group on Ataxic Diseases*

    Original Article 12 April 2008 Pages: 189 - 197

14. Electrophysiology in spinocerebellar ataxias: Spread of disease and characteristic findings

    • Ludger Schöls
    • Christoph Linnemann
    • Christoph Globas

    Original Article 12 April 2008 Pages: 198 - 203

15. Magnetic resonance imaging in spinocerebellar ataxias

    • Susanne Döhlinger
    • Till-Karsten Hauser
    • Jörg B. Schulz

    Original Article 12 April 2008 Pages: 204 - 214

16. Spinocerebellar ataxias caused by polyglutamine expansions: A review of therapeutic strategies

    • Benjamin R. Underwood
    • David C. Rubinsztein

    Original Article 12 April 2008 Pages: 215 - 221