共 50 条
[41]
Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations
[J].
European Journal of Human Genetics,
2004, 12
:441-446
[43]
Quantitative analysis of proton diffusion in olivopontocerebellar degeneration due to SCA1 and SCA2
[J].
RIVISTA DI NEURORADIOLOGIA,
2003, 16
:46-46
[48]
Pathoanatomy of Cerebellar Degeneration in Spinocerebellar Ataxia Type 2 (SCA2) and Type 3 (SCA3)
[J].
The Cerebellum,
2012, 11
:749-760
[50]
Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias
[J].
NEUROLOGIA,
2011, 26 (03)
:157-165