Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease
Abstract Background Spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD) is an autosomal dominant inherited neurodegenerative disorder. Several post-mortem and imaging studies have shown cerebellar and brainstem atrophy. A number of studies have used volumetric regional information to inv...
Main Authors: | Carlos R. Hernandez-Castillo, Rosalinda Diaz, Aurelio Campos-Romo, Juan Fernandez-Ruiz |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2017-06-01
|
Series: | Cerebellum & Ataxias |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s40673-017-0065-7 |
Similar Items
-
Itajaí, Santa Catarina – Azorean ancestry and spinocerebellar ataxia type 3
by: Hélio A. G. Teive, et al. -
The SCA1 (Spinocerebellar ataxia type 1) and MJD (Machado-Joseph disease) CAG repeats in normal individuals: segregation analysis and allele frequencies
by: Cláudia Emília Vieira Wiezel, et al.
Published: (2003-01-01) -
Peripheral Oxidative Stress Biomarkers in Spinocerebellar Ataxia Type 3/Machado–Joseph Disease
by: Adriano M. de Assis, et al.
Published: (2017-09-01) -
Identifying Therapeutic Targets for Spinocerebellar Ataxia Type 3/Machado–Joseph Disease through Integration of Pathological Biomarkers and Therapeutic Strategies
by: Yu-Shuan Chen, et al.
Published: (2020-04-01) -
Assessment of Bone Mineral Density of Patients with Spinocerebellar Ataxia Type 3
by: Aline MS Farias, et al.
Published: (2019-01-01)