Yoshino M - Search Results

1

Studies of urinary organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency.

Kuhara T, Shinka T, Inoue Y, Matsumoto M, Yoshino M, Sakaguchi Y, Matsumoto I. Kuhara T, et al. Among authors: yoshino m. Clin Chim Acta. 1983 Sep 30;133(2):133-40. doi: 10.1016/0009-8981(83)90398-4. Clin Chim Acta. 1983. PMID: 6688766

2

Pyruvate dehydrogenase subcomplex with lipoamide dehydrogenase deficiency in a patient with lactic acidosis and branched chain ketoaciduria.

Matuda S, Kitano A, Sakaguchi Y, Yoshino M, Saheki T. Matuda S, et al. Among authors: yoshino m. Clin Chim Acta. 1984 Jun 27;140(1):59-64. doi: 10.1016/0009-8981(84)90151-7. Clin Chim Acta. 1984. PMID: 6430599

3

Chemical diagnosis of dihydrolipoyl dehydrogenase deficiency.

Kuhara T, Inoue Y, Shinka T, Matsumoto M, Matsumoto I, Yoshino M, Okada S. Kuhara T, et al. Among authors: yoshino m. J Inherit Metab Dis. 1984;7 Suppl 2:115-6. doi: 10.1007/978-94-009-5612-4_32. J Inherit Metab Dis. 1984. PMID: 6434859 No abstract available.

4

Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction.

Sakaguchi Y, Yoshino M, Aramaki S, Yoshida I, Yamashita F, Kuhara T, Matsumoto I, Hayashi T. Sakaguchi Y, et al. Among authors: yoshino m. Eur J Pediatr. 1986 Sep;145(4):271-4. doi: 10.1007/BF00439399. Eur J Pediatr. 1986. PMID: 3769994

5

A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiency.

Yoshino M, Koga Y, Yamashita F. Yoshino M, et al. J Inherit Metab Dis. 1986;9(4):399-400. doi: 10.1007/BF01800493. J Inherit Metab Dis. 1986. PMID: 3104678 No abstract available.

6

An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme: a carboxylase deficiency detected by newborn screening for maple syrup urine disease.

Ihara K, Kuromaru R, Inoue Y, Kuhara T, Matsumoto I, Yoshino M, Fukushige J. Ihara K, et al. Among authors: yoshino m. Eur J Pediatr. 1997 Sep;156(9):713-5. doi: 10.1007/s004310050696. Eur J Pediatr. 1997. PMID: 9296536

7

Maple syrup urine disease: nutritional management by intravenous hyperalimentation and uneventful course after surgical repair of dislocation of the hip.

Koga Y, Iwanaga T, Yoshida I, Yoshino M, Kaneko S, Kato H. Koga Y, et al. Among authors: yoshino m. J Inherit Metab Dis. 1998 Apr;21(2):177-8. doi: 10.1023/a:1005324516186. J Inherit Metab Dis. 1998. PMID: 9584272 No abstract available.

8

Carbonic anhydrase II deficiency in three unrelated Japanese patients.

Aramaki S, Yoshida I, Yoshino M, Kondo M, Sato Y, Noda K, Jo R, Okue A, Sai N, Yamashita F. Aramaki S, et al. Among authors: yoshino m. J Inherit Metab Dis. 1993;16(6):982-90. doi: 10.1007/BF00711514. J Inherit Metab Dis. 1993. PMID: 8127074

9

Potential pitfall of prenatal enzymatic diagnosis of carbamoyl-phosphate synthetase I deficiency.

Yoshino M, Nishiyori A, Koga Y, Mizushima Y, Maeshiro H, Inoue T, Izumi S, Hatase T, Yakushiji M, Kato H. Yoshino M, et al. J Inherit Metab Dis. 1997 Sep;20(5):711-2. doi: 10.1023/a:1005338812965. J Inherit Metab Dis. 1997. PMID: 9323570 No abstract available.

10

Sudden onset of ornithine carbamoyltransferase deficiency after aspirin ingestion.

Yoshida I, Yoshino M, Watanabe J, Yamashita F. Yoshida I, et al. Among authors: yoshino m. J Inherit Metab Dis. 1993;16(5):917. doi: 10.1007/BF00714301. J Inherit Metab Dis. 1993. PMID: 8295421 No abstract available.

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