Kondo N - Search Results

1

Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease).

Isogai K, Sukegawa K, Tomatsu S, Fukao T, Song XQ, Yamada Y, Fukuda S, Orii T, Kondo N. Isogai K, et al. Among authors: kondo n. J Inherit Metab Dis. 1998 Feb;21(1):60-70. doi: 10.1023/a:1005363414792. J Inherit Metab Dis. 1998. PMID: 9501270

2

Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene.

Ogawa T, Tomatsu S, Fukuda S, Yamagishi A, Rezvi GM, Sukegawa K, Kondo N, Suzuki Y, Shimozawa N, Orü T. Ogawa T, et al. Among authors: kondo n. Hum Mol Genet. 1995 Mar;4(3):341-9. doi: 10.1093/hmg/4.3.341. Hum Mol Genet. 1995. PMID: 7795586

3

Molecular analysis by Southern blot for the N-acetylgalactosamine-6-sulphate sulphatase gene causing mucopolysaccharidosis IVA in the Japanese population.

Tomatsu S, Fukuda S, Uchiyama A, Hori T, Nakashima Y, Kondo N, Suzuki Y, Shimozawa N, Sukegawa K, Orii T. Tomatsu S, et al. Among authors: kondo n. J Inherit Metab Dis. 1994;17(5):601-5. doi: 10.1007/BF00711598. J Inherit Metab Dis. 1994. PMID: 7837767 No abstract available.

4

A novel splice site mutation in intron 1 of the GALNS gene in a Japanese patient with mucopolysaccharidosis IVA.

Tomatsu S, Fukuda S, Ogawa T, Kato Z, Isogai K, Kondo N, Suzuki Y, Shimozawa N, Sukegawa K, Orii T. Tomatsu S, et al. Among authors: kondo n. Hum Mol Genet. 1994 Aug;3(8):1427-8. doi: 10.1093/hmg/3.8.1427. Hum Mol Genet. 1994. PMID: 7987329 No abstract available.

5

Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region.

Nakashima Y, Tomatsu S, Hori T, Fukuda S, Sukegawa K, Kondo N, Suzuki Y, Shimozawa N, Orii T. Nakashima Y, et al. Among authors: kondo n. Genomics. 1994 Mar 1;20(1):99-104. doi: 10.1006/geno.1994.1132. Genomics. 1994. PMID: 8020961

6

Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families.

Yamada Y, Tomatsu S, Sukegawa K, Suzuki Y, Kondo N, Hopwood JJ, Orii T. Yamada Y, et al. Among authors: kondo n. Hum Genet. 1993 Sep;92(2):110-4. doi: 10.1007/BF00219675. Hum Genet. 1993. PMID: 8370574 Free article.

7

[Mucopolysaccharidosis type VII: characterization of exonic point mutations and molecular heterogeneity].

Orii T, Tomatsu S, Fukuda S, Sukegawa K, Kondo N. Orii T, et al. Among authors: kondo n. Nihon Rinsho. 1993 Sep;51(9):2330-5. Nihon Rinsho. 1993. PMID: 8411710 Japanese.

8

Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency.

Tomatsu S, Fukuda S, Yamagishi A, Cooper A, Wraith JF, Hori T, Kato Z, Yamada N, Isogai K, Sukegawa K, Kondo N, Suzuki Y, Shimozawa N, Orii T. Tomatsu S, et al. Among authors: kondo n. Am J Hum Genet. 1996 May;58(5):950-62. Am J Hum Genet. 1996. PMID: 8651279 Free PMC article.

9

Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populations.

Yamagishi A, Tomatsu S, Fukuda S, Uchiyama A, Shimozawa N, Suzuki Y, Kondo N, Sukegawa K, Orii T. Yamagishi A, et al. Among authors: kondo n. Hum Mutat. 1996;7(1):23-9. doi: 10.1002/(SICI)1098-1004(1996)7:1<23::AID-HUMU3>3.0.CO;2-Q. Hum Mutat. 1996. PMID: 8664897

10

Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations.

Rezvi GM, Tomatsu S, Fukuda S, Yamagishi A, Cooper A, Wraith JE, Iwata H, Kato Z, Yamada N, Sukegawa K, Shimozawa N, Suzuki Y, Kondo N, Orii T. Rezvi GM, et al. Among authors: kondo n. J Inherit Metab Dis. 1996;19(3):301-8. doi: 10.1007/BF01799258. J Inherit Metab Dis. 1996. PMID: 8803772 Free article.

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