Nishigaki T - Search Results

1

Pulse methylprednisolone with gammaglobulin as an initial treatment for acute Kawasaki disease.

Okada K, Hara J, Maki I, Miki K, Matsuzaki K, Matsuoka T, Yamamoto T, Nishigaki T, Kurotobi S, Sano T; Osaka Kawasaki Disease Study Group. Okada K, et al. Among authors: nishigaki t. Eur J Pediatr. 2009 Feb;168(2):181-5. doi: 10.1007/s00431-008-0727-9. Epub 2008 Apr 30. Eur J Pediatr. 2009. PMID: 18446365

2

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.

Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S. Inui K, et al. Among authors: nishigaki t. J Pediatr. 1992 Jan;120(1):62-6. doi: 10.1016/s0022-3476(05)80599-2. J Pediatr. 1992. PMID: 1370535

3

SSCP analysis by RT-PCR for the prenatal diagnosis of Niemann-Pick disease type C.

Tsukamoto H, Yamamoto T, Nishigaki T, Sakai N, Nanba E, Ninomiya H, Ohno K, Inui K, Okada S. Tsukamoto H, et al. Among authors: nishigaki t. Prenat Diagn. 2001 Jan;21(1):55-7. doi: 10.1002/1097-0223(200101)21:1<55::aid-pd23>3.0.co;2-m. Prenat Diagn. 2001. PMID: 11180242

4

Detection of the A to G(3243) mutation of mitochondrial DNA in Japanese families with mitochondrial encephalomyopathies.

Inui K, Tsukamoto H, Fukushima H, Taniike M, Tanaka J, Nishigaki T, Okada S. Inui K, et al. Among authors: nishigaki t. J Inherit Metab Dis. 1992;15(3):311-4. doi: 10.1007/BF02435964. J Inherit Metab Dis. 1992. PMID: 1405464 No abstract available.

5

Molecular study of Duchenne and Becker muscular dystrophies in Japanese.

Tsukamoto H, Inui K, Fukushima H, Nishigaki T, Taniike M, Tanaka J, Okada S. Tsukamoto H, et al. Among authors: nishigaki t. J Inherit Metab Dis. 1991;14(5):819-24. doi: 10.1007/BF01799956. J Inherit Metab Dis. 1991. PMID: 1779629 No abstract available.

6

Molecular defects in Krabbe disease.

Tatsumi N, Inui K, Sakai N, Fukushima H, Nishimoto J, Yanagihara I, Nishigaki T, Tsukamoto H, Fu L, Taniike M, et al. Tatsumi N, et al. Among authors: nishigaki t. Hum Mol Genet. 1995 Oct;4(10):1865-8. doi: 10.1093/hmg/4.10.1865. Hum Mol Genet. 1995. PMID: 8595408

7

Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's disease.

Sakai N, Inui K, Tatsumi N, Fukushima H, Nishigaki T, Taniike M, Nishimoto J, Tsukamoto H, Yanagihara I, Ozono K, Okada S. Sakai N, et al. Among authors: nishigaki t. J Neurochem. 1996 Mar;66(3):1118-24. doi: 10.1046/j.1471-4159.1996.66031118.x. J Neurochem. 1996. PMID: 8769874

8

Mutation analysis of a Japanese patient with fucosidosis.

Akagi M, Inui K, Nishigaki T, Muramatsu T, Kokubu C, Fu L, Fukushima H, Yanagihara I, Tsukamoto H, Kurahashi H, Okada S. Akagi M, et al. Among authors: nishigaki t. J Hum Genet. 1999;44(5):323-6. doi: 10.1007/s100380050169. J Hum Genet. 1999. PMID: 10496076

9

Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome.

Akagi M, Inui K, Nakajima S, Shima M, Nishigaki T, Muramatsu T, Kokubu C, Tsukamoto H, Sakai N, Okada S. Akagi M, et al. Among authors: nishigaki t. J Hum Genet. 2000;45(1):60-2. doi: 10.1007/s100380050013. J Hum Genet. 2000. PMID: 10697967

10

Mutation analysis of the acid ceramidase gene in Japanese patients with Farber disease.

Muramatsu T, Sakai N, Yanagihara I, Yamada M, Nishigaki T, Kokubu C, Tsukamoto H, Ito M, Inui K. Muramatsu T, et al. Among authors: nishigaki t. J Inherit Metab Dis. 2002 Nov;25(7):585-92. doi: 10.1023/a:1022047408477. J Inherit Metab Dis. 2002. PMID: 12638942

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