| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes
|
Ikeda, Yoshio
|
|
2008
|
7 |
2 |
p. 150-158
|
article
|
| 2 |
Clinical and genetic analysis of spinocerebellar ataxia type 11
|
Johnson, Janel
|
|
2008
|
7 |
2 |
p. 159-164
|
article
|
| 3 |
Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1
|
Matilla-Dueñas, Antoni
|
|
2008
|
7 |
2 |
p. 106-114
|
article
|
| 4 |
Electrophysiology in spinocerebellar ataxias: Spread of disease and characteristic findings
|
Schöls, Ludger
|
|
2008
|
7 |
2 |
p. 198-203
|
article
|
| 5 |
Magnetic resonance imaging in spinocerebellar ataxias
|
Döhlinger, Susanne
|
|
2008
|
7 |
2 |
p. 204-214
|
article
|
| 6 |
Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration
|
Garden, Gwenn A.
|
|
2008
|
7 |
2 |
p. 138-149
|
article
|
| 7 |
SCA13
|
Waters, M. F.
|
|
2008
|
7 |
2 |
p. 165-169
|
article
|
| 8 |
SCA3: Neurological features, pathogenesis and animal models
|
Riess, Olaf
|
|
2008
|
7 |
2 |
p. 125-137
|
article
|
| 9 |
Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21)
|
Delplanque, J.
|
|
2008
|
7 |
2 |
p. 179-183
|
article
|
| 10 |
Spinocerebellar ataxia 2 (SCA2)
|
Lastres-Becker, Isabel
|
|
2008
|
7 |
2 |
p. 115-124
|
article
|
| 11 |
Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4)
|
Stevanin, Giovanni
|
|
2008
|
7 |
2 |
p. 170-178
|
article
|
| 12 |
Spinocerebellar ataxias caused by polyglutamine expansions: A review of therapeutic strategies
|
Underwood, Benjamin R.
|
|
2008
|
7 |
2 |
p. 215-221
|
article
|
| 13 |
Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis
|
Mariotti, Caterina
|
|
2008
|
7 |
2 |
p. 184-188
|
article
|
| 14 |
Sporadic ataxias in Japan – a population-based epidemiological study
|
Tsuji, Shoji
|
|
2008
|
7 |
2 |
p. 189-197
|
article
|
| 15 |
The clinical diagnosis of autosomal dominant spinocerebellar ataxias
|
Klockgether, Thomas
|
|
2008
|
7 |
2 |
p. 101-105
|
article
|
| 16 |
The highly heterogeneous spinocerebellar ataxias: From genes to targets for therapeutic intervention
|
Matilla-Dueñas, Antoni
|
|
2008
|
7 |
2 |
p. 97-100
|
article
|
Journal description