Kobayashi M - Search Results

1

Automated determination of orotic acid, uracil and pseudouridine in urine by high-performance liquid chromatography with column switching.

Ohba S, Kidouchi K, Katoh T, Kibe T, Kobayashi M, Wada Y. Ohba S, et al. Among authors: kobayashi m. J Chromatogr. 1991 Aug 23;568(2):325-32. doi: 10.1016/0378-4347(91)80170-h. J Chromatogr. 1991. PMID: 1783638

2

Reference values of orotic acid, uracil and pseudouridine in urine.

Ohba S, Kidouchi K, Nakamura C, Katoh T, Kobayashi M, Wada Y. Ohba S, et al. Among authors: kobayashi m. Adv Exp Med Biol. 1991;309B:27-30. doi: 10.1007/978-1-4615-7703-4_6. Adv Exp Med Biol. 1991. PMID: 1781382 No abstract available.

3

Urinary acylcarnitines in a patient with neonatal multiple acyl-CoA dehydrogenation deficiency, quantified by a carboxylic acid analyzer with a reversed-phase column.

Kidouchi K, Niwa T, Nohara D, Asai K, Sugiyama N, Morishita H, Kobayashi M, Wada Y. Kidouchi K, et al. Among authors: kobayashi m. Clin Chim Acta. 1988 Apr 29;173(3):263-72. doi: 10.1016/0009-8981(88)90013-7. Clin Chim Acta. 1988. PMID: 3383426

4

Dihydropyrimidinuria: the first case in Japan.

Ohba S, Kidouchi K, Sumi S, Imaeda M, Takeda N, Yoshizumi H, Tatematsu A, Kodama K, Yamanaka K, Kobayashi M, et al. Ohba S, et al. Among authors: kobayashi m. Adv Exp Med Biol. 1994;370:383-6. doi: 10.1007/978-1-4615-2584-4_83. Adv Exp Med Biol. 1994. PMID: 7660934 No abstract available.

5

Urinary propionylcarnitine analysis for monitoring carnitine supplementation in inherited disorders of propionate metabolism.

Sugiyama N, Matsuda I, Wada Y, Narisawa K, Kobayashi M, Kidouchi K. Sugiyama N, et al. Among authors: kobayashi m. J Inherit Metab Dis. 1994;17(5):611-5. doi: 10.1007/BF00711600. J Inherit Metab Dis. 1994. PMID: 7837769 No abstract available.

6

Quantitative analysis of amniotic fluid pyrimidines for the prenatal diagnosis of hereditary orotic aciduria.

Ohba S, Kidouchi K, Toyama J, Oda T, Tsuboi T, Ichiki T, Sobajima H, Sugiyama N, Morishita H, Købayashi M, et al. Ohba S, et al. Among authors: kobayashi m. J Inherit Metab Dis. 1993;16(5):872-5. doi: 10.1007/BF00714281. J Inherit Metab Dis. 1993. PMID: 8295404 No abstract available.

7

Carnitine deficiency in inherited organic acid disorders and Reye syndrome.

Sugiyama N, Kidouchi K, Kobayashi M, Wada Y. Sugiyama N, et al. Among authors: kobayashi m. Acta Paediatr Jpn. 1990 Aug;32(4):410-6. doi: 10.1111/j.1442-200x.1990.tb00854.x. Acta Paediatr Jpn. 1990. PMID: 2288224

8

Analysis of acylcarnitines in maternal urine for prenatal diagnosis of glutaric aciduria type 2.

Sakuma T, Sugiyama N, Ichiki T, Kobayashi M, Wada Y, Nohara D. Sakuma T, et al. Among authors: kobayashi m. Prenat Diagn. 1991 Feb;11(2):77-82. doi: 10.1002/pd.1970110203. Prenat Diagn. 1991. PMID: 2062823

9

Identification of glutarylcarnitine in glutaric aciduria type 1 by carboxylic acid analyzer with an ODS reverse-phase column.

Kidouchi K, Sugiyama N, Morishita H, Kobayashi M, Wada Y, Nohara D. Kidouchi K, et al. Among authors: kobayashi m. Clin Chim Acta. 1987 May 15;164(3):261-6. doi: 10.1016/0009-8981(87)90300-7. Clin Chim Acta. 1987. PMID: 3594917

10

Clinical and molecular heterogeneity in patients with mitochondrial encephalomyopathies due to complex I deficiency.

Ichiki T, Kobayashi M, Wada Y, Tanaka M, Ozawa T. Ichiki T, et al. Among authors: kobayashi m. J Inherit Metab Dis. 1988;11(3):333-6. doi: 10.1007/BF01800387. J Inherit Metab Dis. 1988. PMID: 3148084 No abstract available.

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