Yoshida I - Search Results

1

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: yoshida i. J Inherit Metab Dis. 1993;16(6):982-90. doi: 10.1007/BF00711514. J Inherit Metab Dis. 1993. PMID: 8127074

2

Carbonic anhydrase II deficiency in a Japanese patient produced by a nonsense mutation (TAT-->TAG) at Tyr-40 in exon 2, (Y40X).

Soda H, Yukizane S, Yoshida I, Aramaki S, Kato H. Soda H, et al. Among authors: yoshida i. Hum Mutat. 1995;5(4):348-50. doi: 10.1002/humu.1380050415. Hum Mutat. 1995. PMID: 7627193 No abstract available.

3

Sudden onset of ornithine carbamoyltransferase deficiency after aspirin ingestion.

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

4

A point mutation in exon 3 (His 107-->Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement.

Soda H, Yukizane S, Yoshida I, Koga Y, Aramaki S, Kato H. Soda H, et al. Among authors: yoshida i. Hum Genet. 1996 Apr;97(4):435-7. doi: 10.1007/BF02267062. Hum Genet. 1996. PMID: 8834238

5

Persistent hyperkalaemia in vitamin B12 unresponsive methylmalonic acidaemia.

Morita J, Ito Y, Yoshino M, Koga Y, Yano S, Yoshida I, Yamashita F. Morita J, et al. Among authors: yoshida i. J Inherit Metab Dis. 1989;12(1):89-93. doi: 10.1007/BF01805536. J Inherit Metab Dis. 1989. PMID: 2501589

6

Lipid storage myopathy associated with recurrent Reye syndrome-like attacks, but with a normal carnitine level.

Matsuishi T, Yuge K, Aramaki S, Yoshino M, Yoshida I, Yamashita F. Matsuishi T, et al. Among authors: yoshida i. Brain Dev. 1988;10(2):125-9. doi: 10.1016/s0387-7604(88)80083-4. Brain Dev. 1988. PMID: 3389475

7

Prenatal diagnosis and therapy for a patient with vitamin B12-responsive methylmalonic acidaemia.

Soda H, Ohura T, Yoshida I, Aramaki S, Aoki K, Inokuchi T, Mikami H, Narisawa K. Soda H, et al. Among authors: yoshida i. J Inherit Metab Dis. 1995;18(3):295-8. doi: 10.1007/BF00710418. J Inherit Metab Dis. 1995. PMID: 7474895

8

Renal handling of methylmalonic acid in a uraemic patient with vitamin B12-unresponsive methylmalonic acidaemia.

Soda H, Yoshida I, Aramaki S, Kuriya N, Aoki K, Inokuchi T, Yoshino M, Kato H. Soda H, et al. Among authors: yoshida i. J Inherit Metab Dis. 1996;19(1):90-1. doi: 10.1007/BF01799356. J Inherit Metab Dis. 1996. PMID: 8830186 No abstract available.

9

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: yoshida i. 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.

10

The changing age distribution of Reye's syndrome in the United States and a critique of the CDC criteria.

Yoshida I, Yamashita F. Yoshida I, et al. Acta Paediatr Jpn. 1990 Aug;32(4):378-80. doi: 10.1111/j.1442-200x.1990.tb00848.x. Acta Paediatr Jpn. 1990. PMID: 1963024 No abstract available.

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