Ashizawa T - Search Results

1

ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis.

Li PP, Sun X, Xia G, Arbez N, Paul S, Zhu S, Peng HB, Ross CA, Koeppen AH, Margolis RL, Pulst SM, Ashizawa T, Rudnicki DD. Li PP, et al. Among authors: ashizawa t. Ann Neurol. 2016 Oct;80(4):600-15. doi: 10.1002/ana.24761. Ann Neurol. 2016. PMID: 27531668 Free PMC article.

2

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.

Matsuura T, Achari M, Khajavi M, Bachinski LL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: ashizawa t. Ann Neurol. 1999 Mar;45(3):407-11. doi: 10.1002/1531-8249(199903)45:3<407::aid-ana21>3.0.co;2-d. Ann Neurol. 1999. PMID: 10072060

3

An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia.

Costanzi-Porrini S, Tessarolo D, Abbruzzese C, Liguori M, Ashizawa T, Giacanelli M. Costanzi-Porrini S, et al. Among authors: ashizawa t. Neurology. 2000 Jan 25;54(2):491-3. doi: 10.1212/wnl.54.2.491. Neurology. 2000. PMID: 10668721

4

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: ashizawa t. Nat Genet. 2000 Oct;26(2):191-4. doi: 10.1038/79911. Nat Genet. 2000. PMID: 11017075

5

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.

Rasmussen A, Matsuura T, Ruano L, Yescas P, Ochoa A, Ashizawa T, Alonso E. Rasmussen A, et al. Among authors: ashizawa t. Ann Neurol. 2001 Aug;50(2):234-9. doi: 10.1002/ana.1081. Ann Neurol. 2001. PMID: 11506407

6

Spinocerebellar ataxia type 10 in the French population.

Fujigasaki H, Tardieu S, Camuzat A, Stevanin G, LeGuern E, Matsuura T, Ashizawa T, Dürr A, Brice A. Fujigasaki H, et al. Among authors: ashizawa t. Ann Neurol. 2002 Mar;51(3):408-9. doi: 10.1002/ana.10126. Ann Neurol. 2002. PMID: 11891842 No abstract available.

7

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.

8

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.

Grewal RP, Achari M, Matsuura T, Durazo A, Tayag E, Zu L, Pulst SM, Ashizawa T. Grewal RP, et al. Among authors: ashizawa t. Arch Neurol. 2002 Aug;59(8):1285-90. doi: 10.1001/archneur.59.8.1285. Arch Neurol. 2002. PMID: 12164725

9

[Spinocerebellar ataxia type 10 (SCA10): a disease caused by a novel pentanucleotide repeat expansion].

Ashizawa T, Matsuura T. Ashizawa T, et al. Rinsho Shinkeigaku. 2001 Dec;41(12):1120-2. Rinsho Shinkeigaku. 2001. PMID: 12235814 Review. Japanese.

10

Huntington's disease--like 2 can present as chorea-acanthocytosis.

Walker RH, Rasmussen A, Rudnicki D, Holmes SE, Alonso E, Matsuura T, Ashizawa T, Davidoff-Feldman B, Margolis RL. Walker RH, et al. Among authors: ashizawa t. Neurology. 2003 Oct 14;61(7):1002-4. doi: 10.1212/01.wnl.0000085866.68470.6d. Neurology. 2003. PMID: 14557581

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