Matsuura T - Search Results

1

A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.

Nagamitsu S, Matsuura T, Khajavi M, Armstrong R, Gooch C, Harati Y, Ashizawa T. Nagamitsu S, et al. Among authors: matsuura t. Neurology. 2000 Dec 12;55(11):1697-703. doi: 10.1212/wnl.55.11.1697. Neurology. 2000. PMID: 11113225

2

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

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

3

Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?

Tan EK, Matsuura T, Nagamitsu S, Khajavi M, Jankovic J, Ashizawa T. Tan EK, et al. Among authors: matsuura t. Neurology. 2000 Mar 14;54(5):1195-8. doi: 10.1212/wnl.54.5.1195. Neurology. 2000. PMID: 10720300

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. Neurology. 2002 Mar 26;58(6):983-4. doi: 10.1212/wnl.58.6.983. Neurology. 2002. PMID: 11914424 No abstract available.

5

The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.

Wakamiya M, Matsuura T, Liu Y, Schuster GC, Gao R, Xu W, Sarkar PS, Lin X, Ashizawa T. Wakamiya M, et al. Among authors: matsuura t. Neurology. 2006 Aug 22;67(4):607-13. doi: 10.1212/01.wnl.0000231140.26253.eb. Neurology. 2006. PMID: 16924013

6

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. 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

7

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: matsuura t. Neurology. 2003 Oct 14;61(7):1002-4. doi: 10.1212/01.wnl.0000085866.68470.6d. Neurology. 2003. PMID: 14557581

8

Alcohol dehydrogenase polymorphism and Parkinson's disease.

Tan EK, Nagamitsu S, Matsuura T, Khajavi M, Jankovic J, Ondo W, Ashizawa T. Tan EK, et al. Among authors: matsuura t. Neurosci Lett. 2001 Jun 1;305(1):70-2. doi: 10.1016/s0304-3940(01)01770-0. Neurosci Lett. 2001. PMID: 11356310

9

Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.

Burgess DL, Matsuura T, Ashizawa T, Noebels JL. Burgess DL, et al. Among authors: matsuura t. Epilepsia. 2000 Jan;41(1):24-7. doi: 10.1111/j.1528-1157.2000.tb01500.x. Epilepsia. 2000. PMID: 10643919 Free article.

10

Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.

Swoboda KJ, Soong B, McKenna C, Brunt ER, Litt M, Bale JF Jr, Ashizawa T, Bennett LB, Bowcock AM, Roach ES, Gerson D, Matsuura T, Heydemann PT, Nespeca MP, Jankovic J, Leppert M, Ptácek LJ. Swoboda KJ, et al. Among authors: matsuura t. Neurology. 2000 Jul 25;55(2):224-30. doi: 10.1212/wnl.55.2.224. Neurology. 2000. PMID: 10908896

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