A Rare Case of Type B Neonatal Pyruvate Carboxylase Enzyme Deficiency Presenting With Refractory Lactic Acidosis in the Early Neonatal Period-Reference-Cited by-同舟云学术

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A Rare Case of Type B Neonatal Pyruvate Carboxylase Enzyme Deficiency Presenting With Refractory Lactic Acidosis in the Early Neonatal Period

Published:2022-10-04 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Sharif Saima,Velumula Pradeep Kumar,Boddu Praveen kumar,Altinok Deniz,Fernandes Nithi

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference9 articles.

1. Pyruvate carboxylase deficiency;Wang D,2009

2. Transport of phosphoenolpyruvate by the tricarboxylate transporting system in mammalian mitochondria;Robinson BH;FEBS Lett,1971

3. Phosphoenolpyruvate carboxykinase (GTP): the gene and the enzyme;Hanson RW;Adv Enzymol Relat Areas Mol Biol,1994

4. Structure, mechanism and regulation of pyruvate carboxylase;Jitrapakdee S;Biochem J,2008

5. Feasibility of a mitochondrial pyruvate malate shuttle in pancreatic islets. Further implication of cytosolic NADPH in insulin secretion;MacDonald MJ;J Biol Chem,1995

Cited by 1 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. Case Report: Prenatal neurological injury in a neonate with pyruvate carboxylase deficiency type B;Frontiers in Endocrinology;2023-07-07

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