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xanthurenic acid and Amino Acid Metabolism Disorders, Inborn

xanthurenic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 3 studies

xanthurenic acid : A quinolinemonocarboxylic acid that is quinoline-2-carboxylic acid substituted by hydroxy groups at C-4 and C-8.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Christensen, M1
Duno, M1
Lund, AM1
Skovby, F1
Christensen, E1
Imai, J1
Yoshida, I1
Murayama, K1
Sakai, Y1
Shimizu, H1
Sumi, T1
Iguchi, T1
Kawai, M1
Yamaguchi, S1
Ohura, T1

Reviews

1 review available for xanthurenic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
[Kynureninase deficiency].
    Ryoikibetsu shokogun shirizu, 1998, Issue:18 Pt 1

    Topics: Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Humans; Hydrolases; Kynurenine; Progn

1998

Other Studies

2 other studies available for xanthurenic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:2

    Topics: Adenine; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acid Substitution; Child; DNA Mutation

2007
Determination of the 8-methyl ether of xanthurenic acid in human serum by high-performance liquid chromatography with fluorescence detection.
    Journal of chromatography. B, Biomedical applications, 1996, Apr-26, Volume: 679, Issue:1-2

    Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, High Pressure Liquid; Ethers; Humans; Kynureni

1996