Kuno S - Search Results

1

Influence of monocyte chemoattractant protein 1 gene polymorphism on age at onset of sporadic Parkinson's disease.

Nishimura M, Kuno S, Mizuta I, Ohta M, Maruyama H, Kaji R, Kawakami H. Nishimura M, et al. Among authors: kuno s. Mov Disord. 2003 Aug;18(8):953-5. doi: 10.1002/mds.10462. Mov Disord. 2003. PMID: 12889089

2

Association between dopamine transporter gene polymorphism and susceptibility to Parkinson's disease in Japan.

Nishimura M, Kaji R, Ohta M, Mizuta I, Kuno S. Nishimura M, et al. Among authors: kuno s. Mov Disord. 2002 Jul;17(4):831-2. doi: 10.1002/mds.10187. Mov Disord. 2002. PMID: 12210886

3

Influence of a tumor necrosis factor gene polymorphism in Japanese patients with multiple system atrophy.

Nishimura M, Kuno S, Kaji R, Kawakami H. Nishimura M, et al. Among authors: kuno s. Neurosci Lett. 2005 Feb 21;374(3):218-21. doi: 10.1016/j.neulet.2004.10.056. Neurosci Lett. 2005. PMID: 15663966

4

Glutathione-S-transferase-1 and interleukin-1beta gene polymorphisms in Japanese patients with Parkinson's disease.

Nishimura M, Kuno S, Kaji R, Yasuno K, Kawakami H. Nishimura M, et al. Among authors: kuno s. Mov Disord. 2005 Jul;20(7):901-2. doi: 10.1002/mds.20477. Mov Disord. 2005. PMID: 15834859

5

Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy.

Nishimura M, Kuno S, Kaji R, Kawakami H. Nishimura M, et al. Among authors: kuno s. Mov Disord. 2005 Aug;20(8):1031-3. doi: 10.1002/mds.20491. Mov Disord. 2005. PMID: 15838855

6

Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.

Nishimura M, Kawakami H, Komure O, Maruyama H, Morino H, Izumi Y, Nakamura S, Kaji R, Kuno S. Nishimura M, et al. Among authors: kuno s. Mov Disord. 2002 Jul;17(4):808-11. doi: 10.1002/mds.10124. Mov Disord. 2002. PMID: 12210881

7

Influence of interleukin-1beta gene polymorphisms on age-at-onset of sporadic Parkinson's disease.

Nishimura M, Mizuta I, Mizuta E, Yamasaki S, Ohta M, Kuno S. Nishimura M, et al. Among authors: kuno s. Neurosci Lett. 2000 Apr 21;284(1-2):73-6. doi: 10.1016/s0304-3940(00)00991-5. Neurosci Lett. 2000. PMID: 10771165

8

Meta-analysis of polymorphism of the catechol-O-methyltransferase gene in relation to the etiology of Parkinson's disease in Japan.

Mizuta I, Mizuta E, Yamasaki S, Kuno S, Yasuda M, Tanaka C. Mizuta I, et al. Among authors: kuno s. Mov Disord. 2000 Sep;15(5):1013-4. doi: 10.1002/1531-8257(200009)15:5<1013::aid-mds1040>3.0.co;2-s. Mov Disord. 2000. PMID: 11009216 No abstract available.

9

Influence of interleukin-1beta gene polymorphism on age-at-onset of spinocerebellar ataxia 6 (SCA6) in Japanese patients.

Nishimura M, Kawakami H, Maruyama H, Izumi Y, Kuno S, Kaji R, Nakamura S. Nishimura M, et al. Among authors: kuno s. Neurosci Lett. 2001 Jul 13;307(2):128-30. doi: 10.1016/s0304-3940(01)01934-6. Neurosci Lett. 2001. PMID: 11427317

10

Tumor necrosis factor gene polymorphisms in patients with sporadic Parkinson's disease.

Nishimura M, Mizuta I, Mizuta E, Yamasaki S, Ohta M, Kaji R, Kuno S. Nishimura M, et al. Among authors: kuno s. Neurosci Lett. 2001 Sep 21;311(1):1-4. doi: 10.1016/s0304-3940(01)02111-5. Neurosci Lett. 2001. PMID: 11585553

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