Oshima A - Search Results

1

GM1-gangliosidosis: tandem duplication within exon 3 of beta-galactosidase gene in an infantile patient.

Oshima A, Yoshida K, Ishizaki A, Shimmoto M, Fukuhara Y, Sakuraba H, Suzuki Y. Oshima A, et al. Clin Genet. 1992 May;41(5):235-8. doi: 10.1111/j.1399-0004.1992.tb03672.x. Clin Genet. 1992. PMID: 1606711

2

GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patients.

Yoshida K, Oshima A, Sakuraba H, Nakano T, Yanagisawa N, Inui K, Okada S, Uyama E, Namba R, Kondo K, et al. Yoshida K, et al. Among authors: oshima a. Ann Neurol. 1992 Mar;31(3):328-32. doi: 10.1002/ana.410310316. Ann Neurol. 1992. PMID: 1353343

3

Splicing defect of the glycoasparaginase gene in two Japanese siblings with apartylglucosaminuria.

Yoshida K, Yanagisawa N, Oshima A, Sakuraba H, Iida Y, Suzuki Y. Yoshida K, et al. Among authors: oshima a. Hum Genet. 1992 Sep-Oct;90(1-2):179-80. doi: 10.1007/BF00210771. Hum Genet. 1992. PMID: 1427775

4

Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase A.

Nagao Y, Nakashima H, Fukuhara Y, Shimmoto M, Oshima A, Ikari Y, Mori Y, Sakuraba H, Suzuki Y. Nagao Y, et al. Among authors: oshima a. Clin Genet. 1991 Mar;39(3):233-7. doi: 10.1111/j.1399-0004.1991.tb03018.x. Clin Genet. 1991. PMID: 1645238

5

Clinical and molecular heterogeneity in hereditary beta-galactosidase deficiency.

Suzuki Y, Sakuraba H, Oshima A, Yoshida K, Shimmoto M, Takano T, Fukuhara Y. Suzuki Y, et al. Among authors: oshima a. Dev Neurosci. 1991;13(4-5):299-303. doi: 10.1159/000112201. Dev Neurosci. 1991. PMID: 1817034 Review.

6

Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases.

Yoshida K, Oshima A, Shimmoto M, Fukuhara Y, Sakuraba H, Yanagisawa N, Suzuki Y. Yoshida K, et al. Among authors: oshima a. Am J Hum Genet. 1991 Aug;49(2):435-42. Am J Hum Genet. 1991. PMID: 1907800 Free PMC article.

7

Human beta-galactosidase gene mutations in morquio B disease.

Oshima A, Yoshida K, Shimmoto M, Fukuhara Y, Sakuraba H, Suzuki Y. Oshima A, et al. Am J Hum Genet. 1991 Nov;49(5):1091-3. Am J Hum Genet. 1991. PMID: 1928092 Free PMC article.

8

Beta-galactosidase-deficient human fibroblasts: uptake and processing of the exogenous precursor enzyme expressed by stable transformant COS cells.

Oshima A, Itoh K, Nagao Y, Sakuraba H, Suzuki Y. Oshima A, et al. Hum Genet. 1990 Oct;85(5):505-8. doi: 10.1007/BF00194225. Hum Genet. 1990. PMID: 2121639

9

Partial deletion of human alpha-galactosidase A gene in Fabry disease: direct repeat sequences as a possible cause of slipped mispairing.

Fukuhara Y, Sakuraba H, Oshima A, Shimmoto M, Nagao Y, Nadaoka Y, Suzuki T, Suzuki Y. Fukuhara Y, et al. Among authors: oshima a. Biochem Biophys Res Commun. 1990 Jul 16;170(1):296-300. doi: 10.1016/0006-291x(90)91273-u. Biochem Biophys Res Commun. 1990. PMID: 2164807

10

Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry disease.

Sakuraba H, Oshima A, Fukuhara Y, Shimmoto M, Nagao Y, Bishop DF, Desnick RJ, Suzuki Y. Sakuraba H, et al. Among authors: oshima a. Am J Hum Genet. 1990 Nov;47(5):784-9. Am J Hum Genet. 1990. PMID: 2171331 Free PMC article.

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