The longitudinal progression of MRI changes in pre-ataxic carriers of SCA3/MJD-Reference-Cited by-同舟云学术

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The longitudinal progression of MRI changes in pre-ataxic carriers of SCA3/MJD

Published:2023-05-16 Issue:9 Volume:270 Page:4276-4287
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

de Oliveira Camila Maria,Leotti Vanessa Bielefeldt,Polita Sandra,Anes Mauricio,Cappelli Amanda Henz,Rocha Anastacia Guimarães,Ecco Gabriela,Bolzan Gabriela,Kersting Nathalia,Duarte Juliana Avila,Saraiva-Pereira Maria-Luiza,Junior Marcondes Cavalcante França,Rezende Thiago Junqueira Ribeiro,Jardim Laura Bannach^ORCID

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Hospital de Clínicas de Porto Alegre

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

https://link.springer.com/content/pdf/10.1007/s00415-023-11763-6.pdf

Reference43 articles.

1. Kawaguchi Y, Okamoto T, Taniwaki M et al (1994) CAG expansions in a novel gene for Machado–Joseph disease at chromosome 14q32.1. Nat Genet 8(3):221–228

2. Wu X, Liao X, Zhan Y et al (2017) Microstructural alterations in asymptomatic and symptomatic patients with spinocerebellar ataxia type 3: a tract-based spatial statistics study. Front Neurol 22(8):714

3. Jacobi H, du Montcel ST, Romanzetti S et al (2020) Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study. Lancet Neurol 19(9):738–747

4. de Oliveira CM, Leotti VB, Bolzan G et al (2021) Pre-ataxic changes of clinical scales and eye movement in Machado–Joseph disease: BIGPRO study. Mov Disord 36(4):985–994

5. de Oliveira CM, Leotti VB, Cappelli AH et al (2023) Progression of clinical and eye movement markers in pre-ataxic carriers of Machado–Joseph disease. Mov Disord 38(1):26–34

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