Yoshida I - Search Results

1

Pilot study of gas chromatographic-mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease.

Kuhara T, Shinka T, Inoue Y, Ohse M, Zhen-wei X, Yoshida I, Inokuchi T, Yamaguchi S, Takayanagi M, Matsumoto I. Kuhara T, et al. Among authors: yoshida i. J Chromatogr B Biomed Sci Appl. 1999 Aug 6;731(1):141-7. doi: 10.1016/s0378-4347(99)00205-4. J Chromatogr B Biomed Sci Appl. 1999. PMID: 10492000

2

Neonatal ketosis is not rare: experience of neonatal screening using gas chromatography-mass spectrometry.

Inokuchi T, Yoshida I, Kaneko A, Tashiro K, Tashiro S, Jogo M, Aoki K, Tanaka M. Inokuchi T, et al. Among authors: yoshida i. J Chromatogr B Biomed Sci Appl. 2001 Jul 5;758(1):57-60. doi: 10.1016/s0378-4347(01)00043-3. J Chromatogr B Biomed Sci Appl. 2001. PMID: 11482735

3

Effect of supplementation with L-carnitine at a small dose on acylcarnitine profiles in serum and urine and the renal handling of acylcarnitines in a patient with multiple acyl-coenzyme A dehydrogenation defect.

Yoshino M, Tokunaga Y, Watanabe Y, Yoshida I, Sakaguchi M, Hata I, Shigematsu Y, Kimura M, Yamaguchi S. Yoshino M, et al. Among authors: yoshida i. J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jul 15;792(1):73-82. doi: 10.1016/s1570-0232(03)00310-6. J Chromatogr B Analyt Technol Biomed Life Sci. 2003. PMID: 12828999

4

Determination of the 8-methyl ether of xanthurenic acid in human serum by high-performance liquid chromatography with fluorescence detection.

Imai J, Yoshida I, Murayama K, Sakai Y, Shimizu H, Sumi T, Iguchi T, Kawai M, Yamaguchi S. Imai J, et al. Among authors: yoshida i. J Chromatogr B Biomed Appl. 1996 Apr 26;679(1-2):204-7. doi: 10.1016/0378-4347(95)00572-2. J Chromatogr B Biomed Appl. 1996. PMID: 8998563

5

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

6

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.

7

Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications.

Yorifuji T, Kawai M, Muroi J, Mamada M, Kurokawa K, Shigematsu Y, Hirano S, Sakura N, Yoshida I, Kuhara T, Endo F, Mitsubuchi H, Nakahata T. Yorifuji T, et al. Among authors: yoshida i. Hum Genet. 2002 Aug;111(2):161-5. doi: 10.1007/s00439-002-0761-z. Epub 2002 Jul 4. Hum Genet. 2002. PMID: 12189489

8

Late-onset type II glutaric aciduria with massive pericardial effusion associated with severe fatty liver.

Hirose S, Hamamoto K, Yoshida I, Inokuchi T, Kogo T, Mitsudome A. Hirose S, et al. Among authors: yoshida i. Acta Paediatr. 2000 Jul;89(7):887-8. doi: 10.1080/080352500750043846. Acta Paediatr. 2000. PMID: 10943977 No abstract available.

9

Glycerol kinase deficiency: evidence for complexity in a single gene disorder.

Dipple KM, Zhang YH, Huang BL, McCabe LL, Dallongeville J, Inokuchi T, Kimura M, Marx HJ, Roederer GO, Shih V, Yamaguchi S, Yoshida I, McCabe ER. Dipple KM, et al. Among authors: yoshida i. Hum Genet. 2001 Jul;109(1):55-62. doi: 10.1007/s004390100545. Hum Genet. 2001. PMID: 11479736

10

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: yoshida i. Eur J Pediatr. 1986 Sep;145(4):271-4. doi: 10.1007/BF00439399. Eur J Pediatr. 1986. PMID: 3769994

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