Longitudinal investigation of brain activation during motor tasks in Friedreich ataxia: 24-month data from IMAGE-FRDA
Author:
Funder
Australian National Health and Medical Research Council
Publisher
Springer Science and Business Media LLC
Subject
Histology,General Neuroscience,Anatomy
Link
https://link.springer.com/content/pdf/10.1007/s00429-021-02413-6.pdf
Reference33 articles.
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3. Campuzano V, Montermini L, Molto MD, Pianese L, Cossée M, Cavalcanti F, Monticelli A (1996) Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271(5254):1423–1427. https://doi.org/10.1126/science.271.5254.1423
4. Cocozza S, Costabile T, Tedeschi E, Abate F, Russo C, Liguori A, Filla A (2018) Cognitive and functional connectivity alterations in Friedreich’s ataxia. Ann Clin Transl Neurol 5(6):677–686. https://doi.org/10.1002/acn3.555
5. Corben LA, Delatycki MB, Bradshaw JL, Horne MK, Fahey MC, Churchyard AJ, Georgiou-Karistianis N (2010) Impairment in motor reprogramming in Friedreich ataxia reflecting possible cerebellar dysfunction. J Neurol 257(5):782–791
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Reduced cerebello-cerebral functional connectivity correlates with disease severity and impaired white matter integrity in Friedreich ataxia;Journal of Neurology;2023-03-01
2. A natural history study to track brain and spinal cord changes in individuals with Friedreich’s ataxia: TRACK-FA study protocol;PLOS ONE;2022-11-21
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