propionyl-coenzyme a has been researched along with Inborn Errors of Metabolism in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Carré, G; Charpentier, C; Coudé, FX; Frézal, J; Munnich, A; Ogier, H; Saudubray, JM | 1 |
| Bohan, TP; Hoppel, CL; Maltby, DA; Millington, DS; Roe, CR | 1 |
| Eanes, RZ; McKeon, C; Wolf, B | 1 |
| Iinuma, K; Narisawa, K; Ohura, T; Tada, K | 1 |
| Baumgartner, R; Spaapen, LJ; van der Meer, SB; Wendel, U | 1 |
5 other study(ies) available for propionyl-coenzyme a and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Defective biotin absorption in multiple carboxylase deficiency.
Topics: Acyl Coenzyme A; Biotin; Carbon-Carbon Ligases; Carboxy-Lyases; Humans; Infant; Ligases; Male; Metabolism, Inborn Errors; Propionates; Pyruvate Carboxylase Deficiency Disease | 1981 |
L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemia.
Topics: Acyl Coenzyme A; Adolescent; Carboxy-Lyases; Carnitine; Child; Child, Preschool; Humans; Infant; Male; Mass Spectrometry; Metabolism, Inborn Errors; Methylmalonyl-CoA Decarboxylase; Propionates | 1984 |
Biochemical characterization of propionyl CoA carboxylase deficiency: heterogeneity within a single genetic complementation group.
Topics: Acyl Coenzyme A; Adenosine Triphosphate; Adolescent; Adult; Bicarbonates; Carboxy-Lyases; Child; Child, Preschool; Electrophoresis, Polyacrylamide Gel; Genetic Complementation Test; Humans; Infant; Infant, Newborn; Isoelectric Focusing; Kinetics; Liver; Metabolism, Inborn Errors; Methylmalonyl-CoA Decarboxylase; Middle Aged; Placenta | 1982 |
A novel splicing mutation in propionic acidemia associated with a tetranucleotide direct repeat in the PCCB gene.
Topics: Acyl Coenzyme A; Base Sequence; Carboxy-Lyases; Female; Humans; Japan; Metabolism, Inborn Errors; Methylmalonyl-CoA Decarboxylase; Molecular Sequence Data; Mutation; Propionates; Repetitive Sequences, Nucleic Acid; RNA Splicing | 1995 |
Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism.
Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Fatty Acids; Female; Fetus; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Methylmalonic Acid; Pregnancy; Propionates; Vitamin B 12 | 1991 |