Page last updated: 2024-09-05

butyrylcarnitine and Lipid Metabolism, Inborn Error

butyrylcarnitine has been researched along with Lipid Metabolism, Inborn Error in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Duran, M; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA	1
Abdenur, JE; Barshop, BA; Cederbaum, SD; Chang, E; Deignan, JL; Dorrani, N; Feuchtbaum, L; Gallant, NM; Leydiker, K; Lorey, F; Neidich, J; Puckett, R; Tang, H; Wang, RY	1
Conlon, TJ; Cossette, T; Erger, K; Flotte, TR; Goetzman, E; Gutierrez, G; Matern, D; Owen, R; Vockley, J; Walter, G	1

Trials

1 trial(s) available for butyrylcarnitine and Lipid Metabolism, Inborn Error

Article	Year
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

Article

Year

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

2 other study(ies) available for butyrylcarnitine and Lipid Metabolism, Inborn Error

Article	Year
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California. Molecular genetics and metabolism, 2012, Volume: 106, Issue:1 Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; California; Carnitine; Female; Follow-Up Studies; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Malonates; Neonatal Screening; Sequence Deletion; Succinates	2012
Systemic correction of a fatty acid oxidation defect by intramuscular injection of a recombinant adeno-associated virus vector. Human gene therapy, 2006, Volume: 17, Issue:1 Topics: Animals; Butyryl-CoA Dehydrogenase; Carnitine; Cell Line; Dependovirus; DNA, Recombinant; Fatty Acids; Female; Fibroblasts; Genetic Therapy; Genetic Vectors; Humans; Injections, Intramuscular; Lipid Metabolism, Inborn Errors; Mass Spectrometry; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mitochondria; Muscles; Oxidation-Reduction; Reproducibility of Results; Transduction, Genetic	2006

Article

Year

Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California.

Molecular genetics and metabolism, 2012, Volume: 106, Issue:1

Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; California; Carnitine; Female; Follow-Up Studies; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Malonates; Neonatal Screening; Sequence Deletion; Succinates

2012

Systemic correction of a fatty acid oxidation defect by intramuscular injection of a recombinant adeno-associated virus vector.

Human gene therapy, 2006, Volume: 17, Issue:1

Topics: Animals; Butyryl-CoA Dehydrogenase; Carnitine; Cell Line; Dependovirus; DNA, Recombinant; Fatty Acids; Female; Fibroblasts; Genetic Therapy; Genetic Vectors; Humans; Injections, Intramuscular; Lipid Metabolism, Inborn Errors; Mass Spectrometry; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mitochondria; Muscles; Oxidation-Reduction; Reproducibility of Results; Transduction, Genetic

2006