III．脊髄小脳変性症の治療開発の進歩
Author:
Affiliation:
1. Department of Neurology, Gunma University Graduate School of Medicine
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/naika/111/8/111_1520/_pdf
Reference11 articles.
1. 1) Zu T, et al: Non-ATG-initiated translation directed by microsatellite expansions. Proceedings of the National Academy of Sciences of the United States of America 108: 260-265, 2011.
2. 2) Minakawa EN, et al: Arginine is a disease modifier for polyQ disease models that stabilizes polyQ protein conformation. Brain: a journal of neurology 143: 1811-1825, 2020.
3. 3) Jin JL, et al: Safety and efficacy of umbilical cord mesenchymal stem cell therapy in hereditary spinocerebellar ataxia. Curr Neurovasc Res 10: 11-20, 2013.
4. 4) Nishizawa M, et al: Effect of rovatirelin in patients with cerebellar ataxia: two randomised double-blind placebo-controlled phase 3 trials. Journal of neurology, neurosurgery, and psychiatry 91: 254-262, 2020.
5. 5) Coarelli G, et al: Safety and efficacy of riluzole in spinocerebellar ataxia type 2 in France (ATRIL): a multicentre, randomised, double-blind, placebo-controlled trial. The Lancet Neurology 2022.
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