Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic Carriers-Reference-Cited by-同舟云学术

Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic Carriers

Published:2021-06-09 Issue: Volume: Page:
ISSN:1473-4222
Container-title:The Cerebellum
language:en
Short-container-title:Cerebellum

Author:

Nigri Anna,Sarro Lidia,Mongelli Alessia,Castaldo Anna,Porcu Luca,Pinardi Chiara,Grisoli Marina,Ferraro Stefania,Canafoglia Laura,Visani Elisa,Bruzzone Maria Grazia,Nanetti Lorenzo,Taroni Franco,Mariotti Caterina^ORCID

Funder

Ministero della Salute

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

https://link.springer.com/content/pdf/10.1007/s12311-021-01285-0.pdf

Reference45 articles.

1. Orr HT, Chung MY, Banfi S, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 1993;4:221–6. https://doi.org/10.1038/ng0793-221.

2. Klockgether T, Mariotti C, Paulson HL. Spinocerebellar ataxia. Nat Rev Dis Primers. 2019;5:24. https://doi.org/10.1038/s41572-019-0074-3.

3. Jacobi H, Reetz K, du Montcel ST, et al. Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data. Lancet Neurol. 2013;12:650–8. https://doi.org/10.1016/S1474-4422(13)70104-2.