Kimura M - Search Results

1

[Short-chain acyl-CoA dehydrogenase deficiency].

Kimura M, Yamaguchi S. Kimura M, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):71-3. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596454 Review. Japanese. No abstract available.

2

[2,4-Dienoyl-CoA reductase deficiency].

Kimura M, Yamaguchi S. Kimura M, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):411-3. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590086 Review. Japanese. No abstract available.

3

[Medium-chain acyl-CoA dehydrogenase deficiency].

Kimura M, Yamaguchi S. Kimura M, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):414-6. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590087 Review. Japanese. No abstract available.

4

[Trifunctional protein deficiency and long-chain-3-hydroxy-acyl CoA dehydrogenase deficiency].

Kimura M, Yamaguchi S. Kimura M, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):77-9. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596456 Review. Japanese. No abstract available.

5

Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 15-year-old girl.

Murayama K, Kimura M, Yamaguchi S, Shinka T, Kodama K. Murayama K, et al. Among authors: kimura m. Brain Dev. 1997 Jun;19(4):303-5. doi: 10.1016/s0387-7604(97)86920-3. Brain Dev. 1997. PMID: 9187484

6

Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitonin.

Watanabe H, Yamaguchi S, Kimura M, Wakazono A, Song XQ, Fukao T, Orii T, Hashimoto T. Watanabe H, et al. Among authors: kimura m. Tohoku J Exp Med. 1998 Jan;184(1):29-38. doi: 10.1620/tjem.184.29. Tohoku J Exp Med. 1998. PMID: 9607396 Free article.

7

A case of West syndrome well controlled by very short and low-dose ACTH therapy.

Kimura M, Miyamoto S, Sejima H, Yamaguchi S. Kimura M, et al. Psychiatry Clin Neurosci. 1999 Feb;53(1):67-70. doi: 10.1046/j.1440-1819.1999.00473.x. Psychiatry Clin Neurosci. 1999. PMID: 10201287 Free article.

8

Screening for fatty acid beta oxidation disorders. Acylglycine analysis by electron impact ionization gas chromatography-mass spectrometry.

Kimura M, Yamaguchi S. Kimura M, et al. J Chromatogr B Biomed Sci Appl. 1999 Aug 6;731(1):105-10. doi: 10.1016/s0378-4347(99)00208-x. J Chromatogr B Biomed Sci Appl. 1999. PMID: 10491995

9

Rapid, simplified and sensitive method for screening fructose-1,6-diphosphatase deficiency by analyzing urinary metabolites in urease/direct preparations and gas chromatography-mass spectrometry in the selected-ion monitoring mode.

Iga M, Kimura M, Ohura T, Kikawa Y, Yamaguchi S. Iga M, et al. Among authors: kimura m. J Chromatogr B Biomed Sci Appl. 2000 Sep 1;746(1):75-82. doi: 10.1016/s0378-4347(00)00123-7. J Chromatogr B Biomed Sci Appl. 2000. PMID: 11048742

10

Molecular study of electron transfer flavoprotein alpha-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type II.

Purevjav E, Kimura M, Takusa Y, Ohura T, Tsuchiya M, Hara N, Fukao T, Yamaguchi S. Purevjav E, et al. Among authors: kimura m. Eur J Clin Invest. 2002 Sep;32(9):707-12. doi: 10.1046/j.1365-2362.2002.01045.x. Eur J Clin Invest. 2002. PMID: 12486872

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