Page last updated: 2024-10-18

glycine and Acidemia Propionic

glycine has been researched along with Acidemia Propionic in 3 studies

Research Excerpts

ExcerptRelevanceReference
"Propionic Acidemia (PA) is a rare metabolic disorder caused by the defect in enzyme (propionyl-coenzyme A (CoA) carboxylase) leading to the abnormal accumulation of metabolites of branched-chain amino acid catabolism in blood and urine."4.12A Rare Case of Propionic Acidemia in a Six Months Female Child. ( Aamir, M; Bibi, A; Chaudhry, N; Haroon, ZH; Irum, S; Rehman, A, 2022)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Irum, S1
Rehman, A1
Aamir, M1
Haroon, ZH1
Chaudhry, N1
Bibi, A1
Scholl-Bürgi, S1
Sass, JO1
Zschocke, J1
Karall, D1
Al-Hassnan, ZN1
Boyadjiev, SA1
Praphanphoj, V1
Hamosh, A1
Braverman, NE1
Thomas, GH1
Geraghty, MT1

Reviews

1 review available for glycine and Acidemia Propionic

ArticleYear
Amino acid metabolism in patients with propionic acidaemia.
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Ammonia; Citric Acid Cycle; Diet;

2012

Other Studies

2 other studies available for glycine and Acidemia Propionic

ArticleYear
A Rare Case of Propionic Acidemia in a Six Months Female Child.
    Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2022, Volume: 32, Issue:8

    Topics: Amino Acids, Branched-Chain; Butyric Acid; Citrates; Coenzyme A; Female; Glycine; Humans; Infant; Ke

2022
The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia.
    Journal of inherited metabolic disease, 2003, Volume: 26, Issue:1

    Topics: Acid-Base Equilibrium; Amino Acid Metabolism, Inborn Errors; Bicarbonates; Biomarkers; Diet, Protein

2003