Koike R - Search Results

1

A Japanese family with adrenoleukodystrophy with a codon 291 deletion: a clinical, biochemical, pathological, and genetic report.

Kano S, Watanabe M, Kanai M, Koike R, Onodera O, Tsuji S, Okamoto K, Shoji M. Kano S, et al. Among authors: koike r. J Neurol Sci. 1998 Jun 30;158(2):187-92. doi: 10.1016/s0022-510x(98)00120-8. J Neurol Sci. 1998. PMID: 9702690

2

Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy.

Takano H, Koike R, Onodera O, Sasaki R, Tsuji S. Takano H, et al. Among authors: koike r. Arch Neurol. 1999 Mar;56(3):295-300. doi: 10.1001/archneur.56.3.295. Arch Neurol. 1999. PMID: 10190819

3

Mutational analysis of X-linked adrenoleukodystrophy gene.

Takano H, Koike R, Onodera O, Tsuji S. Takano H, et al. Among authors: koike r. Cell Biochem Biophys. 2000;32 Spring:177-85. doi: 10.1385/cbb:32:1-3:177. Cell Biochem Biophys. 2000. PMID: 11330045 Review.

4

Physiological significance of fatty acid elongation system in adrenoleukodystrophy.

Koike R, Tsuji S, Ohno T, Suzuki Y, Orii T, Miyatake T. Koike R, et al. J Neurol Sci. 1991 Jun;103(2):188-94. doi: 10.1016/0022-510x(91)90163-2. J Neurol Sci. 1991. PMID: 1880537

5

Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients.

Koike R, Onodera O, Tabe H, Kaneko K, Miyatake T, Iwasaki S, Nakano M, Shizuma N, Ikeguchi K, Nishizawa M, et al. Koike R, et al. Hum Mutat. 1995;6(3):263-7. doi: 10.1002/humu.1380060314. Hum Mutat. 1995. PMID: 8535450 No abstract available.

6

[Correlation between degrees of the CTG repeat expansion and clinical features of myotonic dystrophy].

Eguchi I, Koike R, Onodera O, Tanaka K, Kondo H, Tsuji S. Eguchi I, et al. Among authors: koike r. Rinsho Shinkeigaku. 1994 Feb;34(2):118-23. Rinsho Shinkeigaku. 1994. PMID: 8194263 Japanese.

7

CT and MR findings of neuroacanthocytosis.

Okamoto K, Ito J, Furusawa T, Sakai K, Tokiguchi S, Homma A, Koike R, Tsuji S. Okamoto K, et al. Among authors: koike r. J Comput Assist Tomogr. 1997 Mar-Apr;21(2):221-2. doi: 10.1097/00004728-199703000-00010. J Comput Assist Tomogr. 1997. PMID: 9071289 No abstract available.

8

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

Date H, Onodera O, Tanaka H, Iwabuchi K, Uekawa K, Igarashi S, Koike R, Hiroi T, Yuasa T, Awaya Y, Sakai T, Takahashi T, Nagatomo H, Sekijima Y, Kawachi I, Takiyama Y, Nishizawa M, Fukuhara N, Saito K, Sugano S, Tsuji S. Date H, et al. Among authors: koike r. Nat Genet. 2001 Oct;29(2):184-8. doi: 10.1038/ng1001-184. Nat Genet. 2001. PMID: 11586299

9

[A sporadic case of late onset familial amyloidotic polyneuropathy preceded by cardiac involvement].

Aoki K, Koike R, Yuasa T, Ikeda S, Tsuji S. Aoki K, et al. Among authors: koike r. Rinsho Shinkeigaku. 1993 Aug;33(8):905-8. Rinsho Shinkeigaku. 1993. PMID: 8261706 Japanese.

10

Effect of intravenous immunoglobulin in Lambert-Eaton myasthenic syndrome with small-cell lung cancer: correlation with the titer of anti-voltage-gated calcium channel antibody.

Takano H, Tanaka M, Koike R, Nagai H, Arakawa M, Tsuji S. Takano H, et al. Among authors: koike r. Muscle Nerve. 1994 Sep;17(9):1073-5. doi: 10.1002/mus.880170919. Muscle Nerve. 1994. PMID: 8065398 No abstract available.

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