Udaka F - Search Results

1

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).

Matsuyama Z, Kawakami H, Maruyama H, Izumi Y, Komure O, Udaka F, Kameyama M, Nishio T, Kuroda Y, Nishimura M, Nakamura S. Matsuyama Z, et al. Among authors: udaka f. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274

2

SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.

Izumi Y, Maruyama H, Oda M, Morino H, Okada T, Ito H, Sasaki I, Tanaka H, Komure O, Udaka F, Nakamura S, Kawakami H. Izumi Y, et al. Among authors: udaka f. Am J Hum Genet. 2003 Mar;72(3):704-9. doi: 10.1086/367775. Epub 2003 Jan 21. Am J Hum Genet. 2003. PMID: 12545428 Free PMC article.

3

[A sporadic case of spinocerebellar ataxia 6 (SCA 6) with large CAG expansion of the CACNL1A4 gene].

Izumi Y, Sawada H, Matsuyama Z, Kawakami H, Udaka F, Nakamura S, Kameyama M. Izumi Y, et al. Among authors: udaka f. No To Shinkei. 1999 Feb;51(2):167-70. No To Shinkei. 1999. PMID: 10198907 Japanese.

4

Spinocerebellar ataxia type 6 in relation to CAG repeat length.

Kaseda Y, Kawakami H, Matsuyama Z, Kumagai R, Toji M, Komure O, Nishimura M, Izumi Y, Udaka F, Kameyama M, Nishio T, Sunohara N, Kuroda Y, Nakamura S. Kaseda Y, et al. Among authors: udaka f. Acta Neurol Scand. 1999 Apr;99(4):209-12. doi: 10.1111/j.1600-0404.1999.tb07348.x. Acta Neurol Scand. 1999. PMID: 10225349

5

Genetic studies in Parkinson's disease with an alpha-synuclein/NACP gene polymorphism in Japan.

Izumi Y, Morino H, Oda M, Maruyama H, Udaka F, Kameyama M, Nakamura S, Kawakami H. Izumi Y, et al. Among authors: udaka f. Neurosci Lett. 2001 Mar 9;300(2):125-7. doi: 10.1016/s0304-3940(01)01557-9. Neurosci Lett. 2001. PMID: 11207390

6

Miller Fisher-Guillain-Barré overlap syndrome with enhancing lesions in the spinocerebellar tracts.

Urushitani M, Udaka F, Kameyama M. Urushitani M, et al. Among authors: udaka f. J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):241-3. doi: 10.1136/jnnp.58.2.241. J Neurol Neurosurg Psychiatry. 1995. PMID: 7876862 Free PMC article.

7

A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease.

Morino H, Kawarai T, Izumi Y, Kazuta T, Oda M, Komure O, Udaka F, Kameyama M, Nakamura S, Kawakami H. Morino H, et al. Among authors: udaka f. Ann Neurol. 2000 Apr;47(4):528-31. Ann Neurol. 2000. PMID: 10762168 Free article.

8

Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease.

Izumi Y, Miyamoto R, Morino H, Yoshizawa A, Nishinaka K, Udaka F, Kameyama M, Maruyama H, Kawakami H. Izumi Y, et al. Among authors: udaka f. Neurology. 2013 Feb 5;80(6):600-1. doi: 10.1212/WNL.0b013e3182815529. Epub 2013 Jan 16. Neurology. 2013. PMID: 23325900 No abstract available.

9

Cerebellar ataxia with glutamic aciduria.

Sawada H, Seriu N, Udaka F, Kameyama M, Sugiyama H. Sawada H, et al. Among authors: udaka f. Acta Neurol Scand. 1991 Jul;84(1):70-2. doi: 10.1111/j.1600-0404.1991.tb04907.x. Acta Neurol Scand. 1991. PMID: 1681667

10

[Clinical application of magnetic resonance imaging in neurology].

Udaka F, Kameyama M. Udaka F, et al. No To Shinkei. 1988 May;40(5):423-37. No To Shinkei. 1988. PMID: 3415862 Japanese. No abstract available.

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