Lactate/pyruvate in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Author:
Affiliation:
1. Department of Pediatrics; Hiroshima Prefectural Hospital; Hiroshima Japan
2. Department of Pediatrics; Faculty of Medical Sciences; University of Fukui; Eiheiji-cho Fukui Japan
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.13608/fullpdf
Reference5 articles.
1. Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family;Korman;J. Neurol. Sci.,2004
2. The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome;Martinelli;Orphanet J. Rare Dis.,2015
3. Evidence that the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome induce oxidative stress in brain of young rats;Amaral;Int. J. Dev. Neurosci.,2009
4. Dual mechanism of brain damage induced in vivo by the major metabolites accumulating in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome;Viegas;Brain Res.,2011
5. Ornithine and homocitrulline impair mitochondrial function, decrease antioxidant defenses and induce cell death in menadione-stressed rat cortical astrocytes: Potential mechanisms of neurological dysfunction in HHH syndrome;Zanatta;Neurochem. Res.,2016
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings;Metabolic Brain Disease;2024-06-04
2. Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome;Internal Medicine;2021
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