Yoshida K - Search Results

1

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

2

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

3

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.

4

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.

5

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.

6

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

7

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

8

[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.

9

[beta-galactosidosis--GM1 gangliosidosis and Morquio B disease].

Yoshida K, Yanagisawa N. Yoshida K, et al. Nihon Rinsho. 1995 Dec;53(12):2960-6. Nihon Rinsho. 1995. PMID: 8577043 Review. Japanese.

10

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.

Morita H, Ikeda S, Yamamoto K, Morita S, Yoshida K, Nomoto S, Kato M, Yanagisawa N. Morita H, et al. Among authors: yoshida k. Ann Neurol. 1995 May;37(5):646-56. doi: 10.1002/ana.410370515. Ann Neurol. 1995. PMID: 7755360

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