Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference49 articles.
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1. Liver involvement in urea cycle disorders: a review of the literature;Journal of Inherited Metabolic Disease;2017-09-12
2. 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;Neurochemical Research;2016-05-09
3. Ornithine In Vivo Administration Disrupts Redox Homeostasis and Decreases Synaptic Na+, K+-ATPase Activity in Cerebellum of Adolescent Rats: Implications for the Pathogenesis of Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome;Cellular and Molecular Neurobiology;2015-03-13
4. The hyperornithinemia–hyperammonemia-homocitrullinuria syndrome;Orphanet Journal of Rare Diseases;2015-03-11
5. Impairment of brain redox homeostasis caused by the major metabolites accumulating in hyperornithinemia–hyperammonemia–homocitrullinuria syndrome in vivo;Metabolic Brain Disease;2012-07-15
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