carnitine and flavin-adenine dinucleotide

carnitine has been researched along with flavin-adenine dinucleotide in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's1 (14.29)18.2507
2000's1 (14.29)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Singh, I; Singh, RP1
Chance, B; Ernster, L; Garland, PB; Lee, CP; Wong, D1
Angelini, C; Barile, M; Brizio, C; Burlina, AB; Dabbeni-Sala, F; Freda, MP; Nijtmans, L; Vergani, L; Zerbetto, E1
Hasegawa, Y; Kimura, M; Komai, K; Samuraki, M; Terada, N; Yamada, M; Yamaguchi, S1
Duran, M; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA1
Alves, E; Gomes, CM; Henriques, BJ; Martinho, RG; PrudĂȘncio, P; Rocha, H; Rodrigues, JV; Vilarinho, L1
Fukuda, S; Hasegawa, Y; Ito, M; Kobayashi, H; Taketani, T; Yamada, K; Yamaguchi, S1

Trials

1 trial(s) available for carnitine and flavin-adenine dinucleotide

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

6 other study(ies) available for carnitine and flavin-adenine dinucleotide

ArticleYear
Peroxisomal oxidation of lignoceric acid in rat brain.
    Neurochemical research, 1986, Volume: 11, Issue:2

    Topics: Adenosine Triphosphate; Animals; Brain; Carnitine; Coenzyme A; Fatty Acids; Flavin-Adenine Dinucleotide; Hydrogen-Ion Concentration; Microbodies; Mitochondria; NAD; NADP; Oxidation-Reduction; Palmitic Acids; Potassium Cyanide; Rats; Rats, Inbred Strains

1986
Flavoproteins of mitochondrial fatty acid oxidation.
    Proceedings of the National Academy of Sciences of the United States of America, 1967, Volume: 58, Issue:4

    Topics: Animals; Antimycin A; Carnitine; Electron Transport; Fatty Acids; Flavin Mononucleotide; Flavin-Adenine Dinucleotide; Fluorescence; Fluorometry; Kinetics; Membranes; Mitochondria, Liver; NAD; Oxidoreductases; Palmitic Acids; Rats; Spectrophotometry; Succinates

1967
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathies.
    Brain : a journal of neurology, 1999, Volume: 122 ( Pt 12)

    Topics: Adult; Carnitine; Enzyme Activation; Fatty Acid Desaturases; Flavin Mononucleotide; Flavin-Adenine Dinucleotide; Humans; Male; Mitochondria, Muscle; Muscular Diseases; Riboflavin

1999
A successfully treated adult patient with L-2-hydroxyglutaric aciduria.
    Neurology, 2008, Mar-25, Volume: 70, Issue:13

    Topics: Adult; Age Factors; Alcohol Oxidoreductases; Brain; Brain Diseases, Metabolic; Brain Diseases, Metabolic, Inborn; Carnitine; Chromosomes, Human, Pair 14; Female; Flavin-Adenine Dinucleotide; Genetic Markers; Genetic Predisposition to Disease; Homozygote; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Movement Disorders; Treatment Outcome

2008
Mutations at the flavin binding site of ETF:QO yield a MADD-like severe phenotype in Drosophila.
    Biochimica et biophysica acta, 2012, Volume: 1822, Issue:8

    Topics: Alleles; Amino Acid Sequence; Animals; Binding Sites; Carnitine; Drosophila; Electron-Transferring Flavoproteins; Flavin-Adenine Dinucleotide; Flavins; Genotype; Models, Molecular; Molecular Sequence Data; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Mutation; Phenotype

2012
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report.
    Brain & development, 2019, Volume: 41, Issue:7

    Topics: Acyl Coenzyme A; Carnitine; Child, Preschool; Codon, Nonsense; Electron-Transferring Flavoproteins; Flavin-Adenine Dinucleotide; Humans; Male; Membrane Transport Proteins; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Mutation; Receptors, G-Protein-Coupled; Riboflavin

2019