Cargando…
Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1
Autosomal-dominant spinocerebellar ataxias (SCA) are neurodegenerative diseases characterized by progressive ataxia. Here, we report on neurometabolic alterations in spinocerebellar ataxia type 1 (SCA1; SCA-ATXN1) and 14 (SCA14; SCA-PRKCG) assessed by non-invasive (1)H magnetic resonance spectroscop...
Autores principales: | Grosch, Anne Sophie, Rinnenthal, Jan Leo, Rönnefarth, Maria, Lux, Silke, Scheel, Michael, Endres, Matthias, Brandt, Alexander U., Paul, Friedemann, Schmitz-Hübsch, Tanja, Minnerop, Martina, Doss, Sarah |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004522/ https://www.ncbi.nlm.nih.gov/pubmed/33063293 http://dx.doi.org/10.1007/s12311-020-01201-y |
Ejemplares similares
-
Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14
por: Ihl, Thomas, et al.
Publicado: (2020) -
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult‐onset disorder
por: Schmitz‐Hübsch, Tanja, et al.
Publicado: (2021) -
Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1
por: Oertel, Frederike Cosima, et al.
Publicado: (2020) -
Neuropsychological Features of Patients with Spinocerebellar Ataxia (SCA) Types 1, 2, 3, and 6
por: Klinke, Ina, et al.
Publicado: (2010) -
Disease progression of spinocerebellar ataxia types 1, 2, 3 and 6 before and after ataxia onset
por: Jacobi, Heike, et al.
Publicado: (2023)