Nakamura S - Search Results

1

Homozygosity for an allele carrying intermediate CAG repeats in the dentatorubral-pallidoluysian atrophy (DRPLA) gene results in spastic paraplegia.

Kurohara K, Kuroda Y, Maruyama H, Kawakami H, Yukitake M, Matsui M, Nakamura S. Kurohara K, et al. Among authors: nakamura s. Neurology. 1997 Apr;48(4):1087-90. doi: 10.1212/wnl.48.4.1087. Neurology. 1997. PMID: 9109905

2

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

3

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

4

Lack of an association of estrogen receptor alpha gene polymorphisms and transcriptional activity with Alzheimer disease.

Maruyama H, Toji H, Harrington CR, Sasaki K, Izumi Y, Ohnuma T, Arai H, Yasuda M, Tanaka C, Emson PC, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: nakamura s. Arch Neurol. 2000 Feb;57(2):236-40. doi: 10.1001/archneur.57.2.236. Arch Neurol. 2000. PMID: 10681083 Clinical Trial.

5

Lack of an association between cystatin C gene polymorphisms in Japanese patients with Alzheimer's disease.

Maruyama H, Izumi Y, Oda M, Torii T, Morino H, Toji H, Sasaki K, Terasawa H, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: nakamura s. Neurology. 2001 Jul 24;57(2):337-9. doi: 10.1212/wnl.57.2.337. Neurology. 2001. PMID: 11468325

6

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

7

Spinocerebellar ataxia type 6: MRI of three Japanese patients.

Satoh JI, Tokumoto H, Yukitake M, Matsui M, Matsuyama Z, Kawakami H, Nakamura S, Kuroda Y. Satoh JI, et al. Among authors: nakamura s. Neuroradiology. 1998 Apr;40(4):222-7. doi: 10.1007/s002340050571. Neuroradiology. 1998. PMID: 9592791

8

Characteristic magnetic resonance imaging findings in spinocerebellar ataxia 6.

Murata Y, Kawakami H, Yamaguchi S, Nishimura M, Kohriyama T, Ishizaki F, Matsuyama Z, Mimori Y, Nakamura S. Murata Y, et al. Among authors: nakamura s. Arch Neurol. 1998 Oct;55(10):1348-52. doi: 10.1001/archneur.55.10.1348. Arch Neurol. 1998. PMID: 9779664

9

[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.

10

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

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