Nakamura S - Search Results

1

[Molecular genetics of Machado-Joseph disease].

Kawakami H, Maruyama H, Nakamura S. Kawakami H, et al. Among authors: nakamura s. Nihon Rinsho. 1996 Mar;54(3):854-60. Nihon Rinsho. 1996. PMID: 8904248 Review. Japanese.

2

[Electrophysiological findings in patients with SCA6].

Kumagai R, Kaseda Y, Kawakami H, Nakamura S. Kumagai R, et al. Among authors: nakamura s. Nihon Rinsho. 1999 Apr;57(4):886-90. Nihon Rinsho. 1999. PMID: 10222784 Review. Japanese.

3

Variation in the number of CAG repeats in the Machado-Joseph disease gene (MJD1) in the Japanese population.

Matsuyama Z, Kawakami H, Maruyama H, Harada H, Nakata K, Yamaguchi Y, Nakamura S. Matsuyama Z, et al. Among authors: nakamura s. J Neurol Sci. 1999 Jun 15;166(1):71-3. doi: 10.1016/s0022-510x(99)00109-4. J Neurol Sci. 1999. PMID: 10465503

4

CAG repeat length and disease duration in Machado-Joseph disease: a new clinical classification.

Maruyama H, Kawakami H, Kohriyama T, Sakai T, Doyu M, Sobue G, Seto M, Tsujihata M, Oh-i T, Nishio T, Sunohara N, Takahashi R, Ohtake T, Hayashi M, Nishimura M, Saida T, Abe K, Itoyama Y, Matsumoto H, Nakamura S. Maruyama H, et al. Among authors: nakamura s. J Neurol Sci. 1997 Nov 25;152(2):166-71. doi: 10.1016/s0022-510x(97)00155-x. J Neurol Sci. 1997. PMID: 9415538

5

Characteristic magnetic resonance imaging findings in Machado-Joseph disease.

Murata Y, Yamaguchi S, Kawakami H, Imon Y, Maruyama H, Sakai T, Kazuta T, Ohtake T, Nishimura M, Saida T, Chiba S, Oh-i T, Nakamura S. Murata Y, et al. Among authors: nakamura s. Arch Neurol. 1998 Jan;55(1):33-7. doi: 10.1001/archneur.55.1.33. Arch Neurol. 1998. PMID: 9443709

6

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.

Kawaguchi Y, Okamoto T, Taniwaki M, Aizawa M, Inoue M, Katayama S, Kawakami H, Nakamura S, Nishimura M, Akiguchi I, et al. Kawaguchi Y, et al. Among authors: nakamura s. Nat Genet. 1994 Nov;8(3):221-8. doi: 10.1038/ng1194-221. Nat Genet. 1994. PMID: 7874163

7

Reevaluation of the exact CAG repeat length in hereditary cerebellar ataxias using highly denaturing conditions and long PCR.

Maruyama H, Kawakami H, Nakamura S. Maruyama H, et al. Among authors: nakamura s. Hum Genet. 1996 May;97(5):591-5. doi: 10.1007/BF02281866. Hum Genet. 1996. PMID: 8655136

8

A family with Machado-Joseph disease, previously diagnosed as dentatorubral-pallidoluysian atrophy.

Sakai T, Antoku Y, Kawakami H, Maruyama H, Nakamura S, Tanaka K. Sakai T, et al. Among authors: nakamura s. Neurology. 1996 Apr;46(4):1154-6. doi: 10.1212/wnl.46.4.1154. Neurology. 1996. PMID: 8780110

9

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: nakamura s. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274

10

Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease.

Maruyama H, Nakamura S, Matsuyama Z, Sakai T, Doyu M, Sobue G, Seto M, Tsujihata M, Oh-i T, Nishio T, et al. Maruyama H, et al. Among authors: nakamura s. Hum Mol Genet. 1995 May;4(5):807-12. doi: 10.1093/hmg/4.5.807. Hum Mol Genet. 1995. PMID: 7633439

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