Cargando…
Three cases of xanthinuria identified by gas chromatography/mass spectrometry‐based urine metabolomics
INTRODUCTION: Early diagnosis of patients with urolithiasis or hypouricemia owing to inborn errors of hypoxanthine metabolism is important in preventing renal failure or drug‐induced toxicity. CASE PRESENTATION: We identified three patients with xanthinuria using gas chromatography/mass spectrometry...
Autores principales: | Kuhara, Tomiko, Tetsuo, Masahiro, Ohse, Morimasa, Shirakawa, Toshihiko, Nakashima, Yumiko, Yoshiura, Koh‐ichiro, Tanaka, Nagaaki, Taya, Tadashi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622199/ https://www.ncbi.nlm.nih.gov/pubmed/37928284 http://dx.doi.org/10.1002/iju5.12642 |
Ejemplares similares
-
A Biomarker Found in Cadmium Exposed Residents of Thailand by Metabolome Analysis
por: Suvagandha, Dhitiwass, et al.
Publicado: (2014) -
Hereditary xanthinuria in a goat
por: Vail, Krystal J., et al.
Publicado: (2019) -
Mutations Associated with Functional Disorder of Xanthine Oxidoreductase and Hereditary Xanthinuria in Humans
por: Ichida, Kimiyoshi, et al.
Publicado: (2012) -
Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine Oxidoreductase
por: Sekine, Mai, et al.
Publicado: (2021) -
Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function
por: Miyazaki, Satoshi, et al.
Publicado: (2022)