18-6-3-3　ⓔ文献

  1. Harding A: Classification of the hereditary ataxias and paraplegias. Lancet, 1983; 1: 1151–1155.

  2. Orr HT, Chung MY, et al: Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nature Genet, 1993; 4: 221–226.

  3. Tsuji S, Onodera O, et al: Sporadic ataxias in Japan–a population–based epidemiological study. Cerebellum, 2008; 7: 189–197.

  4. Ishikawa K, Mizusawa H: The chromosome 16q–linked autosomal dominant cerebellar ataxia (16q–ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell: The 50th Anniversary of Japanese Society of Neuropathology. Neuropathology, 2010; 30: 490–494.

  5. Daughters RS, Tuttle DL, et al: RNA gain–of–function in spinocerebellar ataxia type 8. PLoS Genet, 2009; 5: e1000600.

  6. Zu T, Gibbens B, et al: Non–ATG–initiated translation directed by microsatellite expansions. Proc Natl Acad Sci USA, 2011; 108: 260–265.

  7. Banez–Coronel M, Ayhan F, et al: RAN translation in Huntington disease. Neuron, 2015; 88: 667–677.

  8. Rossi M, Perez–Lloret S, et al: Autosomal dominant cerebellar ataxias: a systematic review of clinical features. Eur J Neurol, 2014; 21: 607–615.

  9. Yasui K, Yabe I, et al: A 3–year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan. Orphanet J Rare Dis, 2014; 9: 118.

  10. Miyai I, Ito M, et al: Cerebellar ataxia rehabilitation trial in degenerative cerebellar diseases. Neurorehabil Neural Repair, 2012; 26: 515–522.