carnitine and benzoic acid

carnitine has been researched along with benzoic acid in 18 studies

Research

Studies (18)

TimeframeStudies, this research(%)All Research%
pre-19905 (27.78)18.7374
1990's12 (66.67)18.2507
2000's1 (5.56)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ali, A; Qureshi, IA1
Sakuma, T1
Michalak, A; Qureshi, IA4
Asai, K; Ichiki, T; Kidouchi, K; Sakuma, T; Sugiyama, N; Wada, Y1
Ahern, DA; Mitchell, ME1
Bachmann, C; Baerlocher, K; Hochreutener, H; Issakainen, J1
Matsuda, I; Ohtani, Y; Ohyanagi, K; Yamamoto, S1
Costell, M; Grisolía, S; O'Connor, JE1
Cleary, MA; Walter, JH; Wraith, JE1
Butterworth, RF; Qureshi, IA; Ratnakumari, L1
Brummond, MR; Kahler, SG; Kishnani, P; Lachiewicz, AM; Millington, DS; Muenzer, J; Summar, ML; Van Hove, JL; Wenstrup, RJ1
Dallaire, L; Feoli-Fonseca, JC; Lambert, M; Melançon, SB; Millington, DS; Mitchell, G; Qureshi, IA1
Kanazu, T; Yamaguchi, T1
Bonocore, G; Buonocore, G; Ciani, F; Donati, MA; Pasquini, E; Shih, VE; Zammarchi, E1
Chien, YH; Hwu, WL; Law, LK; Lee, NC; Lin, CY; Tang, NL1

Trials

1 trial(s) available for carnitine and benzoic acid

ArticleYear
Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal.
    Biochemical and molecular medicine, 1996, Volume: 57, Issue:1

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Child; Child, Preschool; Female; Humans; Male; Nitrogen; Ornithine; Retrospective Studies; Syndrome; Urea

1996

Other Studies

17 other study(ies) available for carnitine and benzoic acid

ArticleYear
Benzoyl-CoA ligase activity in the liver and kidney cortex of weanling guinea pigs treated with various inducers: relationship with hippurate synthesis and carnitine levels.
    Developmental pharmacology and therapeutics, 1992, Volume: 18, Issue:1-2

    Topics: Animals; Benzoates; Benzoic Acid; Body Weight; Carnitine; Coenzyme A Ligases; Guinea Pigs; Hippurates; Kidney; Liver; Methylprednisolone; Organ Size; Phenobarbital; Sodium Salicylate

1992
Alteration of urinary carnitine profile induced by benzoate administration.
    Archives of disease in childhood, 1991, Volume: 66, Issue:7

    Topics: Acetylcarnitine; Administration, Oral; Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Child, Preschool; Dose-Response Relationship, Drug; Hippurates; Humans; Male

1991
Plasma and urinary levels of carnitine in different experimental models of hyperammonemia and the effect of sodium benzoate treatment.
    Biochemical medicine and metabolic biology, 1990, Volume: 43, Issue:2

    Topics: Ammonia; Animals; Benzoates; Benzoic Acid; Carnitine; Mice; Mice, Mutant Strains

1990
Identification of benzoylcarnitine in the urine of a patient of hyperammonemia.
    The Tohoku journal of experimental medicine, 1989, Volume: 159, Issue:2

    Topics: Ammonia; Benzoates; Benzoic Acid; Carbamoyl-Phosphate Synthase (Ammonia); Carnitine; Humans

1989
Liver function in protein-energy malnutrition measured by cinnamic acid tolerance and benzoic acid tolerance: effect of carnitine supplementation.
    The British journal of nutrition, 1989, Volume: 61, Issue:2

    Topics: Animals; Benzoates; Benzoic Acid; Carnitine; Cinnamates; Drug Tolerance; Fatty Liver; Kwashiorkor; Liver Function Tests; Male; Rats; Rats, Inbred Strains

1989
[Carbamyl phosphate synthase deficiency: clinical symptoms, diagnosis and dietary-medicamentous treatment in the neonatal period and infancy].
    Helvetica paediatrica acta, 1989, Volume: 43, Issue:5-6

    Topics: Amino Acids; Ammonia; Arginine; Benzoates; Benzoic Acid; Carbamoyl-Phosphate Synthase (Ammonia); Carnitine; Citrulline; Combined Modality Therapy; Dietary Proteins; Female; Fetal Growth Retardation; Humans; Infant, Newborn; Male; Pregnancy

1989
Hyperammonemia related to carnitine metabolism with particular emphasis on ornithine transcarbamylase deficiency.
    Enzyme, 1987, Volume: 38, Issue:1-4

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Child; Dietary Proteins; Humans; Reye Syndrome

1987
The potentiation of ammonia toxicity by sodium benzoate is prevented by L-carnitine.
    Biochemical and biophysical research communications, 1987, Jun-15, Volume: 145, Issue:2

    Topics: Ammonia; Animals; Benzoates; Benzoic Acid; Carnitine; Drug Synergism; Glutamates; Male; Mice; Mitochondria, Liver; Urea

1987
Absence of acidosis in the initial presentation of propionic acidaemia.
    Archives of disease in childhood. Fetal and neonatal edition, 1995, Volume: 72, Issue:3

    Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Food Preservatives; Humans; Infant, Newborn; Liver Transplantation; Nervous System Diseases; Propionates

1995
Effect of L-carnitine on cerebral and hepatic energy metabolites in congenitally hyperammonemic sparse-fur mice and its role during benzoate therapy.
    Metabolism: clinical and experimental, 1993, Volume: 42, Issue:8

    Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Benzoates; Benzoic Acid; Body Weight; Brain; Brain Chemistry; Carnitine; Coenzyme A; Dose-Response Relationship, Drug; Energy Metabolism; Genetic Linkage; Glutamates; Glutamic Acid; Glutamine; Hair Diseases; Ketoglutaric Acids; Lactates; Liver; Male; Mice; Mice, Mutant Strains; Ornithine Carbamoyltransferase; Pyruvates; Time Factors; Urea

1993
[Profile of hepatic and muscular acylcarnitines in chronically hyperammonemic mice after an acute treatment with sodium benzoate: dose-response study].
    Annales de biologie clinique, 1993, Volume: 51, Issue:10-11

    Topics: Acetylcarnitine; Ammonia; Animals; Benzoates; Benzoic Acid; Carnitine; Dose-Response Relationship, Drug; Liver; Male; Mice; Mice, Mutant Strains; Muscles

1993
[Carnitine levels in muscle in mice with hyperammonemia: effect of treatment with sodium benzoate].
    Canadian journal of physiology and pharmacology, 1993, Volume: 71, Issue:7

    Topics: Ammonia; Animals; Benzoates; Benzoic Acid; Carnitine; Creatine Kinase; Female; Male; Mice; Mice, Inbred ICR; Muscles

1993
Tissue acylcarnitine and acyl-coenzyme A profiles in chronically hyperammonemic mice treated with sodium benzoate and supplementary L-carnitine.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 1995, Volume: 49, Issue:7-8

    Topics: Acetylcarnitine; Acyl Coenzyme A; Ammonia; Animals; Benzoates; Benzoic Acid; Carnitine; Chronic Disease; Creatine Kinase; Drug Therapy, Combination; Food Preservatives; Liver; Mice; Mice, Mutant Strains; Muscle, Skeletal

1995
Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia.
    American journal of medical genetics, 1995, Dec-04, Volume: 59, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Benzoates; Benzoic Acid; Carnitine; Drug Interactions; Female; Food Preservatives; Glycine; Humans; Infant; Infant, Newborn; Male

1995
Comparison of in vitro carnitine and glycine conjugation with branched-side chain and cyclic side chain carboxylic acids in rats.
    Drug metabolism and disposition: the biological fate of chemicals, 1997, Volume: 25, Issue:2

    Topics: Animals; Benzoates; Benzoic Acid; Butyrates; Carboxylic Acids; Carnitine; Cells, Cultured; Cyclopropanes; Glycine; Isobutyrates; Kidney; Liver; Male; Rats; Rats, Sprague-Dawley

1997
Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcome.
    The Journal of pediatrics, 1997, Volume: 131, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Citrulline; Diet, Protein-Restricted; Humans; Infant, Newborn; Male; Ornithine

1997
Deficiency of the carnitine transporter (OCTN2) with partial N-acetylglutamate synthase (NAGS) deficiency.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:5

    Topics: Amino-Acid N-Acetyltransferase; Benzoic Acid; Carnitine; Child, Preschool; Dietary Supplements; Fatal Outcome; Humans; Male; Metabolism, Inborn Errors; Mutation; Organic Cation Transport Proteins; Phenylbutyrates; Solute Carrier Family 22 Member 5

2007