Page last updated: 2024-09-05

butyrylcarnitine and riboflavin

butyrylcarnitine has been researched along with riboflavin in 2 studies

Compound Research Comparison

Studies
(butyrylcarnitine)
Trials
(butyrylcarnitine)
Recent Studies (post-2010)
(butyrylcarnitine)
Studies
(riboflavin)
Trials
(riboflavin)
Recent Studies (post-2010) (riboflavin)
292139,3453893,015

Protein Interaction Comparison

ProteinTaxonomybutyrylcarnitine (IC50)riboflavin (IC50)
Thiosulfate sulfurtransferaseHomo sapiens (human)8.8

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Duran, M; Hogeveen, M; Ijlst, L; Niezen-Koning, KE; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA1
Duran, M; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA1

Trials

1 trial(s) available for butyrylcarnitine and riboflavin

ArticleYear
Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency.
    Pediatric research, 2010, Volume: 67, Issue:3

    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

Other Studies

1 other study(ies) available for butyrylcarnitine and riboflavin

ArticleYear
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiency.
    JAMA, 2006, Aug-23, Volume: 296, Issue:8

    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