A Unique Case of Pyruvate Carboxylase Deficiency
Author:
Publisher
Cureus, Inc.
Subject
Aerospace Engineering
Reference13 articles.
1. "Pyruvate carboxylase, structure and function";Valle M;Subcell Biochem,2017
2. Pyruvate carboxylase deficiency type c: a rare cause of acute transient flaccid paralysis with ketoacidosis;Almomen M;Neuropediatrics,2018
3. Pyruvate carboxylase deficiency: an underestimated cause of lactic acidosis;Habarou F;Mol Genet Metab Rep,2015
4. Pyruvate carboxylase deficiency;Wang D
5. Inborn errors of carbohydrate, ammonia, amino acid, and organic acid metabolism;Cederbaum S,2012
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1. Long-term chronic food-derived arsenic exposure induce the urinary system metabolic dysfunction in mice;Science of The Total Environment;2023-11
2. Case Report: Prenatal neurological injury in a neonate with pyruvate carboxylase deficiency type B;Frontiers in Endocrinology;2023-07-07
3. The Presence of Pyruvate Carboxylase in the Human Brain and its Role in the Survival of Cultured Human Astrocytes;Physiological Research;2023-06-30
4. Dioctyl phthalate enhances volatile fatty acids production from sludge anaerobic fermentation: Insights of electron transport and metabolic functions;Science of The Total Environment;2023-02
5. PC Splice-Site Variant c.1825+5G>A Caused Intron Retention in a Patient With Pyruvate Carboxylase Deficiency: A Case Report;Frontiers in Pediatrics;2022-04-28
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