Eto Y - Search Results

1

Diaminobenzidine peroxidase in rat brain.

Yamaguchi S, Eto Y. Yamaguchi S, et al. Among authors: eto y. Exp Neurol. 1983 Apr;80(1):1-8. doi: 10.1016/0014-4886(83)90001-8. Exp Neurol. 1983. PMID: 6832264

2

Pathochemical study of a case of hereditary cerebral degenerative disease--lipopigment accumulation and peroxidase deficiency in brain.

Yamaguchi S, Okuno A, Eto Y, Maekawa K. Yamaguchi S, et al. Among authors: eto y. Tohoku J Exp Med. 1985 Feb;145(2):223-9. doi: 10.1620/tjem.145.223. Tohoku J Exp Med. 1985. PMID: 3992585 Free article.

3

Prenatal diagnosis of metachromatic leukodystrophy: a diagnosis by amniotic fluid and its confirmation.

Eto Y, Tahara T, Koda N, Yamaguchi S, Ito F, Okuno A. Eto Y, et al. Arch Neurol. 1982 Jan;39(1):29-32. doi: 10.1001/archneur.1982.00510130031007. Arch Neurol. 1982. PMID: 6119972

4

Clinical and biochemical studies of Japanese neuronal ceroid-lipofuscinosis.

Eto Y, Tsuda T, Ohhashi T, Yamaguchi S, Okuno A. Eto Y, et al. Am J Med Genet Suppl. 1988;5:59-67. doi: 10.1002/ajmg.1320310609. Am J Med Genet Suppl. 1988. PMID: 3146330

5

Abnormal excretion of autofluorescent lipids in urine from patients with neuronal ceroid lipofuscinosis.

Ohashi T, Kanamoto Y, Yamaguchi S, Eto Y, Maekawa K. Ohashi T, et al. Among authors: eto y. Tohoku J Exp Med. 1986 Apr;148(4):335-9. doi: 10.1620/tjem.148.335. Tohoku J Exp Med. 1986. PMID: 3738902 Free article.

6

Prenatal diagnosis of metachromatic leukodystrophy: a diagnosis with amniotic fluid by DEAE-Sepharose column chromatography and its confirmation by kidney lipid analysis.

Eto Y, Tahara T, Koda N, Yamaguchi S. Eto Y, et al. J Inherit Metab Dis. 1982;5(2):77-8. doi: 10.1007/BF01799995. J Inherit Metab Dis. 1982. PMID: 6820428 No abstract available.

7

Revised method of 1H-NMR urinalysis for detecting inborn errors of metabolism.

Yamamoto H, Koda N, Yamaguchi S, Eto Y, Aoki K. Yamamoto H, et al. Among authors: eto y. Clin Chem. 1987 May;33(5):714-5. Clin Chem. 1987. PMID: 3568367 No abstract available.

8

Quick screening and diagnosis of organic acidemia by NMR urinalysis.

Yamaguchi S, Koda N, Eto Y, Aoki K. Yamaguchi S, et al. Among authors: eto y. J Pediatr. 1985 Apr;106(4):620-2. doi: 10.1016/s0022-3476(85)80088-3. J Pediatr. 1985. PMID: 3981318 No abstract available.

9

Rapid screening of metabolic disease by proton NMR urinalysis.

Yamaguchi S, Koda N, Eto Y, Aoki K. Yamaguchi S, et al. Among authors: eto y. Lancet. 1984 Aug 4;2(8397):284. doi: 10.1016/s0140-6736(84)90322-2. Lancet. 1984. PMID: 6146830 No abstract available.

10

Partial deficiency of beta-hexosaminidase activity in canine GM2-gangliosidosis.

Eto Y, Ida H, Umezawa F, Ohashi T, Gomibuchi I, Maekawa K. Eto Y, et al. Tohoku J Exp Med. 1987 Aug;152(4):333-8. doi: 10.1620/tjem.152.333. Tohoku J Exp Med. 1987. PMID: 2958961 Free article.

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