Cargando…
Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease
BACKGROUND: Spinocerebellar ataxia (SCA) type 8 (SCA8) is an inherited neurodegenerative disorder caused by the expansion of untranslated CTA/CTG triplet repeats on 13q21. The phenomenology of SCA8 is relatively varied when compared to the other types of SCAs and its spectrum is not well established...
Autores principales: | Kim, Ji Sun, Son, Tae Ok, Youn, Jinyoung, Ki, Chang-Seok, Cho, Jin Whan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840139/ https://www.ncbi.nlm.nih.gov/pubmed/24285970 http://dx.doi.org/10.3988/jcn.2013.9.4.274 |
Ejemplares similares
-
VEGF ameliorates the ataxic phenotype in spinocerebellar ataxia type 1 (SCA1) mice
por: Cvetanovic, Marija, et al.
Publicado: (2011) -
Mimickers of Amyotrophic Lateral Sclerosis
por: Dubey, Ayush, et al.
Publicado: (2019) -
The longitudinal progression of MRI changes in pre-ataxic carriers of SCA3/MJD
por: de Oliveira, Camila Maria, et al.
Publicado: (2023) -
Ataxic Nystagmus in Disseminated Sclerosis
Publicado: (1944) -
Pre-ataxic loss of intrinsic plasticity and motor learning in a mouse model of SCA1
por: Osório, Catarina, et al.
Publicado: (2022)