Udaka F - Search Results

1

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

2

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.

3

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.

4

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

5

Metaiodobenzylguanidine (MIBG) scintigraphy at various parts of the body in Parkinson's disease and multiple system atrophy.

Matsui H, Udaka F, Oda M, Kubori T, Nishinaka K, Kameyama M. Matsui H, et al. Among authors: udaka f. Auton Neurosci. 2005 Apr 29;119(1):56-60. doi: 10.1016/j.autneu.2005.03.003. Epub 2005 Apr 20. Auton Neurosci. 2005. PMID: 15893708

6

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

7

[A case of inflammatory myopathy worsened by miscarriage with autoimmune disorder-associated disease].

Oda M, Udaka F, Izumi Y, Sakaguchi K, Kaido M, Kameyama M. Oda M, et al. Among authors: udaka f. No To Shinkei. 2001 Apr;53(4):369-72. No To Shinkei. 2001. PMID: 11360477 Japanese.

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

Cerebral white matter lesions are not associated with apoE genotype but with age and female sex in Alzheimer's disease.

Sawada H, Udaka F, Izumi Y, Nishinaka K, Kawakami H, Nakamura S, Kameyama M. Sawada H, et al. Among authors: udaka f. J Neurol Neurosurg Psychiatry. 2000 May;68(5):653-6. doi: 10.1136/jnnp.68.5.653. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766901 Free PMC article.

10

The relation between visual hallucinations and visual evoked potential in Parkinson disease.

Matsui H, Udaka F, Tamura A, Oda M, Kubori T, Nishinaka K, Kameyama M. Matsui H, et al. Among authors: udaka f. Clin Neuropharmacol. 2005 Mar-Apr;28(2):79-82. doi: 10.1097/01.wnf.0000157066.50948.65. Clin Neuropharmacol. 2005. PMID: 15795550

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