Inui K - Search Results

1

[Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].

Tsukamoto H, Inui K, Okada S. Tsukamoto H, et al. Among authors: inui k. Nihon Rinsho. 1993 Sep;51(9):2428-34. Nihon Rinsho. 1993. PMID: 8105117 Review. Japanese.

2

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: inui k. J Inherit Metab Dis. 1991;14(5):819-24. doi: 10.1007/BF01799956. J Inherit Metab Dis. 1991. PMID: 1779629 No abstract available.

3

One base deletion in the cysteine-rich domain of the dystrophin gene in Duchenne muscular dystrophy patients.

Tsukamoto H, Inui K, Matsuoka T, Yanagihara I, Fukushima H, Okada S. Tsukamoto H, et al. Among authors: inui k. Hum Mol Genet. 1994 Jun;3(6):995-6. doi: 10.1093/hmg/3.6.995. Hum Mol Genet. 1994. PMID: 7951251 No abstract available.

4

Gene therapy in Duchenne muscular dystrophy.

Inui K, Okada S, Dickson G. Inui K, et al. Brain Dev. 1996 Sep-Oct;18(5):357-61. doi: 10.1016/0387-7604(96)00043-5. Brain Dev. 1996. PMID: 8891229 Review.

5

Allele frequencies of intragenic, and 5' and 3' markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy.

Tsukamoto H, Inui K, Fukushima H, Okada S. Tsukamoto H, et al. Among authors: inui k. Jpn J Hum Genet. 1996 Dec;41(4):391-7. doi: 10.1007/BF01876329. Jpn J Hum Genet. 1996. PMID: 9088109

6

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: inui k. 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

7

[Peripheral neuropathy in two children with mitochondrial encephalomyopathy].

Tanaka J, Taniike M, Inui K, Nagai T, Okada S. Tanaka J, et al. Among authors: inui k. Rinsho Shinkeigaku. 1991 Jul;31(7):772-4. Rinsho Shinkeigaku. 1991. PMID: 1664789 Japanese.

8

A family with pseudodeficiency of acid alpha-glucosidase.

Nishimoto J, Inui K, Okada S, Ishigami W, Hirota S, Yamano T, Yabuuchi H. Nishimoto J, et al. Among authors: inui k. Clin Genet. 1988 Apr;33(4):254-61. doi: 10.1111/j.1399-0004.1988.tb03446.x. Clin Genet. 1988. PMID: 3282727

9

Different clinical features in monozygotic twins: a case of 7q--syndrome.

Tsukamoto H, Inui K, Taniike M, Kamiyama K, Hori M, Sumi K, Okada S. Tsukamoto H, et al. Among authors: inui k. Clin Genet. 1993 Mar;43(3):139-42. doi: 10.1111/j.1399-0004.1993.tb04438.x. Clin Genet. 1993. PMID: 7684659

10

[Krabbe disease (globoid cell leukodystrophy)].

Sakai N, Inui K, Okada S. Sakai N, et al. Among authors: inui k. Nihon Rinsho. 1995 Dec;53(12):2947-51. Nihon Rinsho. 1995. PMID: 8577041 Review. Japanese.

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