Maruyama H - Search Results

1

[Age-related changes in amplitude ratio, duration ratio and area ratio in nerve conduction studies].

Kurokawa K, Tanaka E, Yamashita H, Nakayama T, Maruyama H, Yukawa M, Kohriyama T, Mimori Y, Nakamura S. Kurokawa K, et al. Among authors: maruyama h. Nihon Ronen Igakkai Zasshi. 1995 Aug-Sep;32(8-9):547-52. doi: 10.3143/geriatrics.32.547. Nihon Ronen Igakkai Zasshi. 1995. PMID: 8531399 Free article. Japanese.

2

[A case of multiple sclerosis associated with lateralization of bone change].

Maruyama H, Sakata C, Harada A, Ishizaki F, Nakamura S. Maruyama H, et al. Nihon Ronen Igakkai Zasshi. 1995 Jun;32(6):442-5. doi: 10.3143/geriatrics.32.442. Nihon Ronen Igakkai Zasshi. 1995. PMID: 7563940 Free article. Japanese.

3

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. Hum Mol Genet. 1995 May;4(5):807-12. doi: 10.1093/hmg/4.5.807. Hum Mol Genet. 1995. PMID: 7633439

4

[Age-related difficulty in rhythmic movement].

Hashizume K, Nagasaki H, Ito H, Furuna T, Sugiura M, Kinugasa T, Maruyama H. Hashizume K, et al. Among authors: maruyama h. Nihon Ronen Igakkai Zasshi. 1994 May;31(5):360-5. doi: 10.3143/geriatrics.31.360. Nihon Ronen Igakkai Zasshi. 1994. PMID: 8072206 Free article. Japanese.

5

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. Hum Genet. 1996 May;97(5):591-5. doi: 10.1007/BF02281866. Hum Genet. 1996. PMID: 8655136

6

Cloning and expression of a rat brain basic helix-loop-helix factor.

Kawakami H, Maruyama H, Yasunami M, Ohkubo H, Hara H, Saida T, Nakanishi S, Nakamura S. Kawakami H, et al. Among authors: maruyama h. Biochem Biophys Res Commun. 1996 Apr 5;221(1):199-204. doi: 10.1006/bbrc.1996.0569. Biochem Biophys Res Commun. 1996. PMID: 8660336

7

[Molecular genetics of Machado-Joseph disease].

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

8

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: maruyama h. Neurology. 1997 Apr;48(4):1087-90. doi: 10.1212/wnl.48.4.1087. Neurology. 1997. PMID: 9109905

9

[Endothelial cell activation and/or injury in multiple sclerosis: analysis with von Willebrand factor and thrombomodulin].

Kohriyama T, Maruyama H, Kurokawa K, Harada T, Nakamura S. Kohriyama T, et al. Among authors: maruyama h. Rinsho Shinkeigaku. 1997 Apr;37(4):287-91. Rinsho Shinkeigaku. 1997. PMID: 9248336 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: maruyama h. 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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