Progressive subcortical involvement as spinocerebellar ataxia type 3 advances
Abstract Background and objectives Spinocerebellar ataxia type 3 (SCA3) is a progressive neurodegenerative disease characterized by heterogeneous motor and nonmotor manifestations. The progressive pattern of subcortical shape abnormalities and their associations with the clinical phenotypes in SCA3...
Saved in:
| Main Authors: | Pubing Yuan, Yonghua Huang, Minghui Dai, Xin Jin, Dingxin Zheng, Die Xiao, Lihua Deng, Peiling Ou, Linfeng Shi, Yifan Chen, Jian Wang, Wei Chen, Yuanchao Zhang, Chen Liu |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2025-06-01
|
| Series: | Orphanet Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13023-025-03803-3 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohortResearch in context
by: Moritz Berger, et al.
Published: (2025-08-01) -
Magnetic resonance imaging for spinocerebellar ataxia: a bibliometric analysis based on web of science
by: Zhen-Yi Liu, et al.
Published: (2025-07-01) -
ATXN3: a multifunctional protein involved in the polyglutamine disease spinocerebellar ataxia type 3
by: Esperanza Hernández-Carralero, et al.
Published: (2024-01-01) -
Effects of trace element dysregulation on brain structure and function in spinocerebellar Ataxia type 3
by: LiHua Deng, et al.
Published: (2025-04-01) -
Professor Wadia’s contributions to neurology and spinocerebellar ataxia type 2
by: Fernando Spina Tensini, et al.