Yoshida K - 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. Among authors: yoshida k. 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. 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. Hum Genet. 1992 Sep-Oct;90(1-2):179-80. doi: 10.1007/BF00210771. Hum Genet. 1992. PMID: 1427775

4

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: yoshida k. Dev Neurosci. 1991;13(4-5):299-303. doi: 10.1159/000112201. Dev Neurosci. 1991. PMID: 1817034 Review.

5

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. Am J Hum Genet. 1991 Aug;49(2):435-42. Am J Hum Genet. 1991. PMID: 1907800 Free PMC article.

6

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. Among authors: yoshida k. Am J Hum Genet. 1991 Nov;49(5):1091-3. Am J Hum Genet. 1991. PMID: 1928092 Free PMC article.

7

Molecular cloning and sequence analysis of cDNAs coding for guinea pig alpha 1-antiproteinases S and F and contrapsin.

Suzuki Y, Yoshida K, Honda E, Sinohara H. Suzuki Y, et al. Among authors: yoshida k. J Biol Chem. 1991 Jan 15;266(2):928-32. J Biol Chem. 1991. PMID: 1985973 Free article.

8

Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7.

Naritomi K, Izumikawa Y, Ohshiro S, Yoshida K, Shimozawa N, Suzuki Y, Orii T, Hirayama K. Naritomi K, et al. Among authors: yoshida k. Hum Genet. 1989 Dec;84(1):79-80. doi: 10.1007/BF00210677. Hum Genet. 1989. PMID: 2606480

9

[Molecular genetics of beta-galactosidase deficiency (GM1-gangliosidosis and Morquio syndrome type B)].

Yoshida K, Yanagisawa N. Yoshida K, et al. Nihon Rinsho. 1993 Sep;51(9):2269-75. Nihon Rinsho. 1993. PMID: 8411701 Review. Japanese.

10

Adult GM1 gangliosidosis: immunohistochemical and ultrastructural findings in an autopsy case.

Yoshida K, Ikeda S, Kawaguchi K, Yanagisawa N. Yoshida K, et al. Neurology. 1994 Dec;44(12):2376-82. doi: 10.1212/wnl.44.12.2376. Neurology. 1994. PMID: 7991129

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