Progression of Cerebellar Atrophy in Spinocerebellar Ataxia Type 2 Gene Carriers: A Longitudinal MRI Study in Preclinical and Early Disease Stages.
cerebellar lobule segmentation
cerebellar structural MRI
cognitive assessment
cortical thickness
pre-symptomatic gene carriers
spinocerebellar ataxia (SCA2)
symbol digit modalities test
Journal
Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899
Informations de publication
Date de publication:
2020
2020
Historique:
received:
13
10
2020
accepted:
17
11
2020
entrez:
1
1
2021
pubmed:
2
1
2021
medline:
2
1
2021
Statut:
epublish
Résumé
Spinocerebellar ataxias type 2 (SCA2) is an autosomal dominant inherited disease caused by expanded trinucleotide repeats (≥32 CAG) within the coding region of
Identifiants
pubmed: 33384659
doi: 10.3389/fneur.2020.616419
pmc: PMC7770103
doi:
Types de publication
Journal Article
Langues
eng
Pagination
616419Informations de copyright
Copyright © 2020 Nigri, Sarro, Mongelli, Pinardi, Porcu, Castaldo, Ferraro, Grisoli, Bruzzone, Gellera, Taroni, Mariotti and Nanetti.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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