butyrylcarnitine has been researched along with riboflavin in 2 studies
Studies (butyrylcarnitine) | Trials (butyrylcarnitine) | Recent Studies (post-2010) (butyrylcarnitine) | Studies (riboflavin) | Trials (riboflavin) | Recent Studies (post-2010) (riboflavin) |
---|---|---|---|---|---|
29 | 2 | 13 | 9,345 | 389 | 3,015 |
Protein | Taxonomy | butyrylcarnitine (IC50) | riboflavin (IC50) |
---|---|---|---|
Thiosulfate sulfurtransferase | Homo sapiens (human) | 8.8 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Duran, M; Hogeveen, M; Ijlst, L; Niezen-Koning, KE; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA | 1 |
Duran, M; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA | 1 |
1 trial(s) available for butyrylcarnitine and riboflavin
Article | Year |
---|---|
Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency.
Topics: Adolescent; Biomarkers; Butyryl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Female; Flavin-Adenine Dinucleotide; Genetic Predisposition to Disease; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Malonates; Mutation; Phenotype; Prospective Studies; Riboflavin; Treatment Outcome; Vitamin B Complex | 2010 |
1 other study(ies) available for butyrylcarnitine and riboflavin
Article | Year |
---|---|
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Carnitine; Child; Child, Preschool; Female; Genotype; Humans; Infant; Infant, Newborn; Male; Malonates; Metabolism, Inborn Errors; Mutation; Neonatal Screening; Netherlands; Phenotype; Retrospective Studies; Riboflavin; Vitamin B Complex | 2006 |