Page last updated: 2024-08-17

acetyl coenzyme a and Amino Acid Metabolism Disorders, Inborn

acetyl coenzyme a has been researched along with Amino Acid Metabolism Disorders, Inborn in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gunay-Aygun, M1
Brandt, U; Dröse, S; Hoffmann, GF; Kölker, S; Nijtmans, LG; Okun, JG; Rodenburg, RJ; Sauer, SW; Schwab, MA; Smeitink, JA; Ter Laak, H; van den Heuvel, LP1
Kuhara, T; Matsumoto, I; Matsuo, M; Shinka, T1
Stewart, PM; Walser, M1
Bartlett, K; Gompertz, D1

Reviews

1 review(s) available for acetyl coenzyme a and Amino Acid Metabolism Disorders, Inborn

ArticleYear
3-Methylglutaconic aciduria: a common biochemical marker in various syndromes with diverse clinical features.
    Molecular genetics and metabolism, 2005, Volume: 84, Issue:1

    Topics: Abnormalities, Multiple; Acetyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Glutarates; Humans; Hydro-Lyases; Leucine; Mitochondrial Diseases; Sterols

2005

Other Studies

4 other study(ies) available for acetyl coenzyme a and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins.
    The Biochemical journal, 2006, Aug-15, Volume: 398, Issue:1

    Topics: Acetyl Coenzyme A; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Animals; Cattle; Energy Metabolism; Fatty Acids; Female; Fibroblasts; Humans; Infant, Newborn; Male; Mitochondrial Diseases; Oxidative Phosphorylation; Propionates; Pyruvate Dehydrogenase Complex; Quadriceps Muscle; Skin; Swine; Toxins, Biological

2006
Increased excretion of four acetyl-CoA precursors during clinical episode of propionic acidaemia.
    Journal of inherited metabolic disease, 1982, Volume: 5, Issue:4

    Topics: Acetyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant; Leucine; Propionates

1982
Low dose ethanol prevents propionate induced hyperammonemia.
    Biochemical and biophysical research communications, 1981, Volume: 100, Issue:4

    Topics: Acetyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Carbamoyl-Phosphate Synthase (Ammonia); Ethanol; Female; Glutamates; Liver; Propionates; Rats

1981
The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemias.
    Biochemical medicine, 1974, Volume: 10, Issue:1

    Topics: Acetyl Coenzyme A; Acyltransferases; Amino Acid Metabolism, Inborn Errors; Animals; Benzoates; Butyrates; Cattle; Chromatography, Gel; Chromatography, Ion Exchange; Computers; Crotonates; Glycine; Kinetics; Malonates; Mitochondria, Liver; Propionates; Regression Analysis; Spectrophotometry; Spectrophotometry, Ultraviolet; Valerates

1974