Kato T - Search Results

1

A case of late variant form of infantile Krabbe disease with a partial deficiency of galactocerebrosidase.

Okada S, Kato T, Tanaka H, Takada K, Aramitsu Y. Okada S, et al. Among authors: kato t. Brain Dev. 1988;10(1):45-6. doi: 10.1016/s0387-7604(88)80045-7. Brain Dev. 1988. PMID: 3369670

2

The complementation of beta-galactosidase in fused cells of mucolipidosis II with another variants of beta-galactosidase deficiency using new single cell enzyme assay.

Okada S, Kato T, Yabuuchi H, Okada Y. Okada S, et al. Among authors: kato t. Biochem Biophys Res Commun. 1979 May 28;88(2):559-62. doi: 10.1016/0006-291x(79)92084-9. Biochem Biophys Res Commun. 1979. PMID: 111672 No abstract available.

3

A case of neuraminidase deficiency associated with a partial beta-galactosidase defect. Clinical, biochemical and radiological studies.

Okada S, Yutaka T, Kato T, Ikehara C, Yabuuchi H, Okawa M, Inui M, Chiyo H. Okada S, et al. Among authors: kato t. Eur J Pediatr. 1979 Apr 3;130(4):239-49. doi: 10.1007/BF00441360. Eur J Pediatr. 1979. PMID: 436849

4

A simple method of lysosomal hydrolase assay in a single somatic cell and its application.

Okada S, Kato T, Yutaka T, Yabuuchi H, Furuyama JI. Okada S, et al. Among authors: kato t. Clin Chim Acta. 1979 Sep 3;96(3):281-4. doi: 10.1016/0009-8981(79)90441-8. Clin Chim Acta. 1979. PMID: 487599

5

beta-Galactosidase deficient-type mucolipidosis: a complementation study of neuraminidase in somatic cell hybrids.

Kato T, Okada S, Yutaka T, Inui K, Yabuuchi H, Chiyo H, Furuyama JI, Okada Y. Kato T, et al. Biochem Biophys Res Commun. 1979 Nov 14;91(1):114-7. doi: 10.1016/0006-291x(79)90590-4. Biochem Biophys Res Commun. 1979. PMID: 518612 No abstract available.

6

Lack of hepatotoxicity or promotion of enzyme-altered liver foci development in rats treated with harman or norharman.

Hagiwara A, Tanaka H, Kurata Y, Kato T, Tsuda H, Ito N. Hagiwara A, et al. Among authors: kato t. J Toxicol Environ Health. 1990;29(2):211-8. doi: 10.1080/15287399009531384. J Toxicol Environ Health. 1990. PMID: 2299694

7

Biochemical heterogeneity in I-cell disease. Sucrose-loading test classifies two distinct subtypes.

Okada S, Inui K, Furukawa M, Midorikawa M, Nishimoto J, Yabuuchi H, Kato T, Watanabe M, Gasa S, Makita A. Okada S, et al. Among authors: kato t. Enzyme. 1987;38(1-4):267-72. doi: 10.1159/000469215. Enzyme. 1987. PMID: 2831041

8

Diagnosis of Pompe's disease using pyridylamino-maltooligosaccharides as substrates of alpha-1,4-glucosidase.

Midorikawa M, Okada S, Kato T, Yutaka T, Yabuuchi H. Midorikawa M, et al. Among authors: kato t. Clin Chim Acta. 1985 Apr 15;147(2):97-102. doi: 10.1016/0009-8981(85)90069-5. Clin Chim Acta. 1985. PMID: 3886206

9

Degradation of keratan sulfate by beta-N-acetylhexosaminidases in GM2-gangliosidosis.

Yutaka T, Okada S, Kato T, Yabuuhi H. Yutaka T, et al. Among authors: kato t. Clin Genet. 1982 Mar;21(3):196-202. doi: 10.1111/j.1399-0004.1982.tb00963.x. Clin Genet. 1982. PMID: 6212169

10

Impaired degradation of keratan sulfate in GM1-gangliosidosis.

Yutaka T, Okada S, Kato T, Yabuuchi H. Yutaka T, et al. Among authors: kato t. Clin Chim Acta. 1982 Oct 27;125(2):233-40. doi: 10.1016/0009-8981(82)90199-1. Clin Chim Acta. 1982. PMID: 6216030 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

12,692 results

Search Page

Filters