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Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study.
Nakamura K, Yoshida K, Matsushima A, Shimizu Y, Sato S, Yahikozawa H, Ohara S, Yazawa M, Ushiyama M, Sato M, Morita H, Inoue A, Ikeda SI. Nakamura K, et al. Cerebellum. 2017 Apr;16(2):518-524. doi: 10.1007/s12311-016-0833-6. Cerebellum. 2017. PMID: 27830516
Spinocerebellar ataxia type 31 (SCA31) is known as a late-onset, relatively pure cerebellar form of ataxia, but a longitudinal prospective study on the natural history of SCA31 has not been done yet. ...
Spinocerebellar ataxia type 31 (SCA31) is known as a late-onset, relatively pure cerebellar form of ataxia, but …
Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31.
Yabe I, Matsushima M, Yoshida K, Ishikawa K, Shirai S, Takahashi I, Sasaki H. Yabe I, et al. J Neurol Sci. 2015 Mar 15;350(1-2):90-2. doi: 10.1016/j.jns.2014.12.042. Epub 2015 Jan 5. J Neurol Sci. 2015. PMID: 25684342 Free article.
Spinocerebellar ataxia type 31 (SCA31) and spinocerebellar ataxia type 6 (SCA6) are the most frequent types of spinocerebellar degeneration in Japan. ...
Spinocerebellar ataxia type 31 (SCA31) and spinocerebellar ataxia type 6 (SCA6) are the most frequent types of s …
Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan.
Sakai H, Yoshida K, Shimizu Y, Morita H, Ikeda S, Matsumoto N. Sakai H, et al. Neurogenetics. 2010 Oct;11(4):409-15. doi: 10.1007/s10048-010-0245-6. Epub 2010 Apr 28. Neurogenetics. 2010. PMID: 20424877 Free PMC article.
Spinocerebellar ataxia type 31 (SCA31) is a recently defined subtype of autosomal dominant cerebellar ataxia (ADCA) characterized by adult-onset, pure cerebellar ataxia. ...
Spinocerebellar ataxia type 31 (SCA31) is a recently defined subtype of autosomal dominant cerebellar ataxia (AD …
Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians.
Ishikawa K, Dürr A, Klopstock T, Müller S, De Toffol B, Vidailhet M, Vighetto A, Marelli C, Wichmann HE, Illig T, Niimi Y, Sato N, Amino T, Stevanin G, Brice A, Mizusawa H. Ishikawa K, et al. Neurology. 2011 Nov 15;77(20):1853-5. doi: 10.1212/WNL.0b013e3182377e3a. Epub 2011 Nov 2. Neurology. 2011. PMID: 22049201 No abstract available.
Comparisons of acoustic function in SCA31 and other forms of ataxias.
Ikeda Y, Nagai M, Kurata T, Yamashita T, Ohta Y, Nagotani S, Deguchi K, Takehisa Y, Shiro Y, Matsuura T, Abe K. Ikeda Y, et al. Neurol Res. 2011 May;33(4):427-32. doi: 10.1179/1743132810Y.0000000011. Neurol Res. 2011. PMID: 21535943
OBJECTIVE: To investigate whether acoustic impairment can be one of the characteristic extracerebellar symptoms in sporadic and hereditary ataxias including spinocerebellar ataxia type 31 (SCA31). METHODS: We investigated genotypes of dominant ataxia f …
OBJECTIVE: To investigate whether acoustic impairment can be one of the characteristic extracerebellar symptoms in sporadic and hereditary a …
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31.
Ishiguro T, Sato N, Ueyama M, Fujikake N, Sellier C, Kanegami A, Tokuda E, Zamiri B, Gall-Duncan T, Mirceta M, Furukawa Y, Yokota T, Wada K, Taylor JP, Pearson CE, Charlet-Berguerand N, Mizusawa H, Nagai Y, Ishikawa K. Ishiguro T, et al. Neuron. 2017 Apr 5;94(1):108-124.e7. doi: 10.1016/j.neuron.2017.02.046. Epub 2017 Mar 23. Neuron. 2017. PMID: 28343865 Free PMC article.
We report that expression of expanded UGGAA (UGGAA(exp)) repeats, responsible for spinocerebellar ataxia type 31 (SCA31) in Drosophila, causes neurodegeneration accompanied by accumulation of UGGAA(exp) RNA foci and translation of repeat-associated pen …
We report that expression of expanded UGGAA (UGGAA(exp)) repeats, responsible for spinocerebellar ataxia type 31 …