Page last updated: 2024-10-16

carnitine and Cerebro-Hepato-Renal Syndrome

carnitine has been researched along with Cerebro-Hepato-Renal Syndrome in 6 studies

Research Excerpts

ExcerptRelevanceReference
" Due to the importance of L-carnitine in intermediary metabolism we studied the effects of L-carnitine on healthy human skin fibroblasts and fibroblasts without functional peroxisomes (Zellweger Syndrome) cultivated under carnitine deficiency, which is caused by standard media compositions."3.72L-Carnitine alters nitric oxide synthase activity in fibroblasts depending on the peroxisomal status. ( Koeck, T; Kremser, K, 2003)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Klouwer, FCC1
Ferdinandusse, S1
van Lenthe, H1
Kulik, W1
Wanders, RJA1
Poll-The, BT1
Waterham, HR1
Vaz, FM1
Duranti, G1
Boenzi, S1
Rizzo, C1
RavĂ , L1
Di Ciommo, V1
Carrozzo, R1
Meschini, MC1
Johnson, DW1
Dionisi-Vici, C1
Koeck, T1
Kremser, K1
Chegary, M1
Te Brinke, H1
Doolaard, M1
Ijlst, L1
Wijburg, FA1
Wanders, RJ1
Houten, SM1
Shimizu, N1
Yamaguchi, S1
Orii, T1
Johnson, AW1
Mills, K1
Clayton, PT1

Other Studies

6 other studies available for carnitine and Cerebro-Hepato-Renal Syndrome

ArticleYear
Evaluation of C26:0-lysophosphatidylcholine and C26:0-carnitine as diagnostic markers for Zellweger spectrum disorders.
    Journal of inherited metabolic disease, 2017, Volume: 40, Issue:6

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Biomarkers; Carnitine; Case-Control Studies; Child; Chil

2017
Urine acylcarnitine analysis by ESI-MS/MS: a new tool for the diagnosis of peroxisomal biogenesis disorders.
    Clinica chimica acta; international journal of clinical chemistry, 2008, Volume: 398, Issue:1-2

    Topics: Carnitine; Female; Humans; Infant; Infant, Newborn; Male; Peroxisomal Disorders; Refsum Disease; Rep

2008
L-Carnitine alters nitric oxide synthase activity in fibroblasts depending on the peroxisomal status.
    The international journal of biochemistry & cell biology, 2003, Volume: 35, Issue:2

    Topics: Acetylcysteine; Animals; Antioxidants; Carnitine; Cattle; Cells, Cultured; Fatty Acids; Fibroblasts;

2003
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidation.
    Molecular genetics and metabolism, 2008, Volume: 93, Issue:4

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetyl-CoA C-Acyltransferase; Acyl-CoA Dehydrogenase, Long-Chain;

2008
A study of urinary metabolites in patients with dicarboxylic aciduria for differential diagnosis.
    Acta paediatrica Japonica : Overseas edition, 1994, Volume: 36, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Diagnosis, Differential; Dicarbox

1994
The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots.
    Biochemical Society transactions, 1996, Volume: 24, Issue:3

    Topics: Biliary Atresia; Carnitine; Child; Fatty Acid Desaturases; Humans; Infant, Newborn; Maple Syrup Urin

1996