Increased pyroglutamic acid levels in patients on artificial diets
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference15 articles.
1. Pyroglutamic Aciduria — a New Inborn Error of Metabolism
2. Pyroglutamic aciduria: Rate of formation and degradation of pyroglutamate
3. PYROGLUTAMIC ACIDURIA Studies in an Infant with Chronic Metabolic Acidosis
4. Pyroglutamic Aciduria (5-Oxoprolinuria), an Inborn Error in Glutathione Metabolism
5. Amino acid levels in patients with hyperammonaemia and argininosuccinic aciduria
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1. Gas Chromatography Mass Spectrometry Aided Diagnosis of Glutathione Synthetase Deficiency;Laboratory Medicine;2021-11-17
2. Pyroglutamic Acidemia: An Underrecognized and Underdiagnosed Cause of High Anion Gap Metabolic Acidosis - A Case Report and Review of Literature;Cureus;2019-07-24
3. Recurrent anion gap metabolic acidosis in a woman with vertebral disc disease;The American Journal of Emergency Medicine;2011-10
4. High anion gap metabolic acidosis secondary to pyroglutamic aciduria (5-oxoprolinuria): association with prescription drugs and malnutrition;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2007-07-01
5. Inborn errors in the metabolism of glutathione;Orphanet Journal of Rare Diseases;2007-03-30
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