nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes
|
Ikeda, Yoshio |
|
2008 |
7 |
2 |
p. 150-158 |
artikel |
2 |
Clinical and genetic analysis of spinocerebellar ataxia type 11
|
Johnson, Janel |
|
2008 |
7 |
2 |
p. 159-164 |
artikel |
3 |
Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1
|
Matilla-Dueñas, Antoni |
|
2008 |
7 |
2 |
p. 106-114 |
artikel |
4 |
Electrophysiology in spinocerebellar ataxias: Spread of disease and characteristic findings
|
Schöls, Ludger |
|
2008 |
7 |
2 |
p. 198-203 |
artikel |
5 |
Magnetic resonance imaging in spinocerebellar ataxias
|
Döhlinger, Susanne |
|
2008 |
7 |
2 |
p. 204-214 |
artikel |
6 |
Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration
|
Garden, Gwenn A. |
|
2008 |
7 |
2 |
p. 138-149 |
artikel |
7 |
SCA13
|
Waters, M. F. |
|
2008 |
7 |
2 |
p. 165-169 |
artikel |
8 |
SCA3: Neurological features, pathogenesis and animal models
|
Riess, Olaf |
|
2008 |
7 |
2 |
p. 125-137 |
artikel |
9 |
Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21)
|
Delplanque, J. |
|
2008 |
7 |
2 |
p. 179-183 |
artikel |
10 |
Spinocerebellar ataxia 2 (SCA2)
|
Lastres-Becker, Isabel |
|
2008 |
7 |
2 |
p. 115-124 |
artikel |
11 |
Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4)
|
Stevanin, Giovanni |
|
2008 |
7 |
2 |
p. 170-178 |
artikel |
12 |
Spinocerebellar ataxias caused by polyglutamine expansions: A review of therapeutic strategies
|
Underwood, Benjamin R. |
|
2008 |
7 |
2 |
p. 215-221 |
artikel |
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 |
artikel |
14 |
Sporadic ataxias in Japan – a population-based epidemiological study
|
Tsuji, Shoji |
|
2008 |
7 |
2 |
p. 189-197 |
artikel |
15 |
The clinical diagnosis of autosomal dominant spinocerebellar ataxias
|
Klockgether, Thomas |
|
2008 |
7 |
2 |
p. 101-105 |
artikel |
16 |
The highly heterogeneous spinocerebellar ataxias: From genes to targets for therapeutic intervention
|
Matilla-Dueñas, Antoni |
|
2008 |
7 |
2 |
p. 97-100 |
artikel |