These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 2380628)

  • 1. Abnormal urinary excretion of unsaturated dicarboxylic acids in patients with medium-chain acyl-CoA dehydrogenase deficiency.
    Tserng KY; Jin SJ; Kerr DS; Hoppel CL
    J Lipid Res; 1990 May; 31(5):763-71. PubMed ID: 2380628
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiency.
    Divry P; Vianey-Liaud C; Cotte J
    J Inherit Metab Dis; 1984; 7 Suppl 1():44-7. PubMed ID: 6434844
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.
    Bennett MJ; Coates PM; Hale DE; Millington DS; Pollitt RJ; Rinaldo P; Roe CR; Tanaka K
    J Inherit Metab Dis; 1990; 13(5):707-15. PubMed ID: 2246856
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Urinary medium-chain acylcarnitines in medium-chain acyl-CoA dehydrogenase deficiency, medium-chain triglyceride feeding and valproic acid therapy: sensitivity and specificity of the radioisotopic exchange/high performance liquid chromatography method.
    Schmidt-Sommerfeld E; Penn D; Rinaldo P; Kossak D; Li BU; Huang ZH; Gage DA
    Pediatr Res; 1992 Jun; 31(6):545-51. PubMed ID: 1635814
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Urinary 3-hydroxydicarboxylic acids in pathophysiology of metabolic disorders with dicarboxylic aciduria.
    Tserng KY; Jin SJ; Kerr DS; Hoppel CL
    Metabolism; 1991 Jul; 40(7):676-82. PubMed ID: 1870421
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency.
    Roe CR; Millington DS; Maltby DA; Bohan TP; Kahler SG; Chalmers RA
    Pediatr Res; 1985 May; 19(5):459-66. PubMed ID: 4000772
    [TBL] [Abstract][Full Text] [Related]  

  • 7. General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.
    Gregersen N; Kølvraa S; Rasmussen K; Mortensen PB; Divry P; David M; Hobolth N
    Clin Chim Acta; 1983 Aug; 132(2):181-91. PubMed ID: 6616873
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
    Rinaldo P; O'Shea JJ; Coates PM; Hale DE; Stanley CA; Tanaka K
    N Engl J Med; 1988 Nov; 319(20):1308-13. PubMed ID: 3054550
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The differential diagnosis of dicarboxylic aciduria.
    Duran M; De Klerk JB; Wadman SK; Bruinvis L; Ketting D
    J Inherit Metab Dis; 1984; 7 Suppl 1():48-51. PubMed ID: 6434845
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids.
    Duran M; Mitchell G; de Klerk JB; de Jager JP; Hofkamp M; Bruinvis L; Ketting D; Saudubray JM; Wadman SK
    J Pediatr; 1985 Sep; 107(3):397-404. PubMed ID: 4032135
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of isomeric unsaturated medium-chain dicarboxylic acids in human urine.
    Jin SJ; Tserng KY
    J Lipid Res; 1989 Oct; 30(10):1611-9. PubMed ID: 2614263
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids.
    Duran M; Ketting D; van Vossen R; Beckeringh TE; Dorland L; Bruinvis L; Wadman SK
    Clin Chim Acta; 1985 Nov; 152(3):253-60. PubMed ID: 4064333
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome.
    Del Valle JA; Garcia MJ; Merinero B; Pérez-Cerdá C; Roman F; Jimenez A; Ugarte M; Martínez-Pardo M; Ludeña C; Camarero C
    J Inherit Metab Dis; 1984; 7(2):62-4. PubMed ID: 6434827
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood.
    Divry P; David M; Gregersen N; Kølvraa S; Christensen E; Collet JP; Dellamonica C; Cotte J
    Acta Paediatr Scand; 1983 Nov; 72(6):943-9. PubMed ID: 6673498
    [TBL] [Abstract][Full Text] [Related]  

  • 15. C6-C10-dicarboxylic aciduria: biochemical considerations in relation to diagnosis of beta-oxidation defects.
    Gregersen N; Kølvraa S; Mortensen PB; Rasmussen K
    Scand J Clin Lab Invest Suppl; 1982; 161():15-27. PubMed ID: 6959231
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency].
    Collet JP; Divry P; Blanc JF; Guibaud P; David M; Macabeo V; Vibert J; Hermier M
    Pediatrie; 1984 Dec; 39(8):661-8. PubMed ID: 6535973
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts.
    Rhead WJ; Amendt BA; Fritchman KS; Felts SJ
    Science; 1983 Jul; 221(4605):73-5. PubMed ID: 6857268
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Metabolic origins of urinary unsaturated dicarboxylic acids.
    Jin SJ; Tserng KY
    Biochemistry; 1990 Sep; 29(37):8540-7. PubMed ID: 2271537
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in 2 patients with symptoms of Reye syndrome].
    Brus F; Smit GP; Knoester H; Reijngoud DJ
    Tijdschr Kindergeneeskd; 1988 Jun; 56(3):132-7. PubMed ID: 3046055
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots.
    Bennett MJ; Ragni MC; Ostfeld RJ; Santer R; Schmidt-Sommerfeld E
    Ann Clin Biochem; 1994 Jan; 31 ( Pt 1)():72-7. PubMed ID: 8154855
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.