Ashizawa T - Search Results

1

CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity.

Perez BA, Shorrock HK, Banez-Coronel M, Zu T, Romano LE, Laboissonniere LA, Reid T, Ikeda Y, Reddy K, Gomez CM, Bird T, Ashizawa T, Schut LJ, Brusco A, Berglund JA, Hasholt LF, Nielsen JE, Subramony SH, Ranum LP. Perez BA, et al. Among authors: ashizawa t. EMBO Mol Med. 2021 Nov 8;13(11):e14095. doi: 10.15252/emmm.202114095. Epub 2021 Oct 11. EMBO Mol Med. 2021. PMID: 34632710 Free PMC article.

2

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.

Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, Dobyns WB, Subramony SH, Zoghbi HY, Lee CC. Zhuchenko O, et al. Among authors: ashizawa t. Nat Genet. 1997 Jan;15(1):62-9. doi: 10.1038/ng0197-62. Nat Genet. 1997. PMID: 8988170

3

What is Kearns-Sayre syndrome after all?

Ashizawa T, Subramony SH. Ashizawa T, et al. Arch Neurol. 2001 Jul;58(7):1053-4. doi: 10.1001/archneur.58.7.1053. Arch Neurol. 2001. PMID: 11448292 No abstract available.

4

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.

Matsuura T, Ranum LP, Volpini V, Pandolfo M, Sasaki H, Tashiro K, Watase K, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: ashizawa t. Neurology. 2002 Mar 26;58(6):983-4. doi: 10.1212/wnl.58.6.983. Neurology. 2002. PMID: 11914424 No abstract available.

5

Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay.

Cagnoli C, Michielotto C, Matsuura T, Ashizawa T, Margolis RL, Holmes SE, Gellera C, Migone N, Brusco A. Cagnoli C, et al. Among authors: ashizawa t. J Mol Diagn. 2004 May;6(2):96-100. doi: 10.1016/S1525-1578(10)60496-5. J Mol Diagn. 2004. PMID: 15096564 Free PMC article.

6

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.

Ikeda Y, Dalton JC, Moseley ML, Gardner KL, Bird TD, Ashizawa T, Seltzer WK, Pandolfo M, Milunsky A, Potter NT, Shoji M, Vincent JB, Day JW, Ranum LP. Ikeda Y, et al. Among authors: ashizawa t. Am J Hum Genet. 2004 Jul;75(1):3-16. doi: 10.1086/422014. Epub 2004 May 19. Am J Hum Genet. 2004. PMID: 15152344 Free PMC article.

7

Measuring Friedreich ataxia: Interrater reliability of a neurologic rating scale.

Subramony SH, May W, Lynch D, Gomez C, Fischbeck K, Hallett M, Taylor P, Wilson R, Ashizawa T; Cooperative Ataxia Group. Subramony SH, et al. Among authors: ashizawa t. Neurology. 2005 Apr 12;64(7):1261-2. doi: 10.1212/01.WNL.0000156802.15466.79. Neurology. 2005. PMID: 15824358

8

Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?

Matsuura T, Fang P, Pearson CE, Jayakar P, Ashizawa T, Roa BB, Nelson DL. Matsuura T, et al. Among authors: ashizawa t. Am J Hum Genet. 2006 Jan;78(1):125-9. doi: 10.1086/498654. Epub 2005 Nov 15. Am J Hum Genet. 2006. PMID: 16385455 Free PMC article.

9

Measuring Friedreich ataxia: complementary features of examination and performance measures.

Lynch DR, Farmer JM, Tsou AY, Perlman S, Subramony SH, Gomez CM, Ashizawa T, Wilmot GR, Wilson RB, Balcer LJ. Lynch DR, et al. Among authors: ashizawa t. Neurology. 2006 Jun 13;66(11):1711-6. doi: 10.1212/01.wnl.0000218155.46739.90. Neurology. 2006. PMID: 16769945 Clinical Trial.

10

Antioxidant use in Friedreich ataxia.

Myers L, Farmer JM, Wilson RB, Friedman L, Tsou A, Perlman SL, Subramony SH, Gomez CM, Ashizawa T, Wilmot GR, Mathews KD, Balcer LJ, Lynch DR. Myers L, et al. Among authors: ashizawa t. J Neurol Sci. 2008 Apr 15;267(1-2):174-6. doi: 10.1016/j.jns.2007.10.008. Epub 2007 Nov 7. J Neurol Sci. 2008. PMID: 17988688 Free PMC article. Clinical Trial.

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