Cargando…
Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in Canada
BACKGROUND: Autosomal dominant (AD) spinocerebellar ataxias (SCAs) encompass a large group of rare disorders, which occurs in individuals of different ethnic backgrounds. To date, demographics, and clinical descriptions of AD SCA in Canada are lacking. METHODS: A retrospective chart review of patien...
Autores principales: | Alshimemeri, Sohaila, Abo Alsamh, Danah, Zhou, Lily, Furtado, Sarah, Kraft, Scott, Bruno, Veronica, Duquette, Antoine, Brais, Bernard, Suchowersky, Oksana, Munhoz, Renato P., Slow, Elizabeth |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026276/ https://www.ncbi.nlm.nih.gov/pubmed/36949783 http://dx.doi.org/10.1002/mdc3.13666 |
Ejemplares similares
-
Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review
por: Park, Jun Young, et al.
Publicado: (2020) -
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
por: Huang, Lijia, et al.
Publicado: (2012) -
Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India
por: Sharma, Shashikant, et al.
Publicado: (2012) -
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
por: Huang, Lijia, et al.
Publicado: (2022) -
Endocannabinoid System in Spinocerebellar Ataxia Type-3 and Other Autosomal-Dominant Cerebellar Ataxias: Potential Role in Pathogenesis and Expected Relevance as Neuroprotective Targets
por: Gómez-Ruiz, María, et al.
Publicado: (2019)