BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 9059968)

  • 1. Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers.
    Elias E; Gray RG; Poulton K; Green A
    J Hepatol; 1997 Feb; 26(2):433-6. PubMed ID: 9059968
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Riboflavin-responsive ethylmalonic-adipic aciduria.
    Green A; Marshall TG; Bennett MJ; Gray RG; Pollitt RJ
    J Inherit Metab Dis; 1985; 8(2):67-70. PubMed ID: 3939533
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy.
    Brivet M; Tardieu M; Khellaf A; Boutron A; Rocchiccioli F; Haengeli CA; Lemonnier A
    J Inherit Metab Dis; 1991; 14(3):333-7. PubMed ID: 1770786
    [No Abstract]   [Full Text] [Related]  

  • 4. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects.
    Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K
    Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency.
    Harpey JP; Charpentier C; Coudé M; Divry P; Paturneau-Jouas M
    J Pediatr; 1987 Jun; 110(6):881-4. PubMed ID: 3585604
    [No Abstract]   [Full Text] [Related]  

  • 6. The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
    Amendt BA; Rhead WJ
    J Clin Invest; 1986 Jul; 78(1):205-13. PubMed ID: 3722376
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Electron-transferring flavoprotein deficiency in the multiple acyl-CoA dehydrogenation disorders, glutaric aciduria type II and ethylmalonic--adipic aciduria.
    Rhead WJ; Amendt BA
    J Inherit Metab Dis; 1984; 7 Suppl 2():99-100. PubMed ID: 6434879
    [No Abstract]   [Full Text] [Related]  

  • 8. Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria).
    Green A; Preece MA; de Sousa C; Pollitt RJ
    J Inherit Metab Dis; 1991; 14(5):691-7. PubMed ID: 1779616
    [TBL] [Abstract][Full Text] [Related]  

  • 9. New defect in fatty-acid metabolism with hypoglycemia and organic aciduria.
    Tanaka K; Mantagos S; Genel M; Seashore MR; Billings BA; Baretz BH
    Lancet; 1977 Nov; 2(8045):986-7. PubMed ID: 72337
    [No Abstract]   [Full Text] [Related]  

  • 10. Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines.
    Rinaldo P; Welch RD; Previs SF; Schmidt-Sommerfeld E; Gargus JJ; O'Shea JJ; Zinn AB
    Pediatr Res; 1991 Sep; 30(3):216-21. PubMed ID: 1945558
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation.
    Harpey JP; Charpentier C; Paturneau-Jouas M
    Biol Neonate; 1990; 58 Suppl 1():70-80. PubMed ID: 2265221
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new case of short-chain acyl-CoA dehydrogenase deficiency with isolated ethylmalonic aciduria.
    Sewell AC; Herwig J; Böhles H; Rinaldo P; Bhala A; Hale DE
    Eur J Pediatr; 1993 Nov; 152(11):922-4. PubMed ID: 8276024
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dicarboxylic aciduria: the response to fasting.
    Truscott RJ; Hick L; Pullin C; Halpern B; Wilcken B; Griffiths H; Silink M; Kilham H; Grunseit F
    Clin Chim Acta; 1979 May; 94(1):31-9. PubMed ID: 455718
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reye syndrome and reye-like syndrome.
    Gosalakkal JA; Kamoji V
    Pediatr Neurol; 2008 Sep; 39(3):198-200. PubMed ID: 18725066
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cannabinoid receptor antagonist-induced striated muscle toxicity and ethylmalonic-adipic aciduria in beagle dogs.
    Tomlinson L; Tirmenstein MA; Janovitz EB; Aranibar N; Ott KH; Kozlosky JC; Patrone LM; Achanzar WE; Augustine KA; Brannen KC; Carlson KE; Charlap JH; Dubrow KM; Kang L; Rosini LT; Panzica-Kelly JM; Flint OP; Moulin FJ; Megill JR; Zhang H; Bennett MJ; Horvath JJ
    Toxicol Sci; 2012 Oct; 129(2):268-79. PubMed ID: 22821849
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiency.
    García-Silva MT; Campos Y; Ribes A; Briones P; Cabello A; Santos Borbujo J; Arenas J; Garavaglia B
    J Pediatr; 1994 Nov; 125(5 Pt 1):843-4. PubMed ID: 7965445
    [No Abstract]   [Full Text] [Related]  

  • 17. Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome.
    Chapoy PR; Angelini C; Brown WJ; Stiff JE; Shug AL; Cederbaum SD
    N Engl J Med; 1980 Dec; 303(24):1389-94. PubMed ID: 7432384
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Letter: Respiratory-distress syndrome of the newborn, Reye's syndrome, and fatty acids.
    Brown RE; Drake RM
    Lancet; 1974 Nov; 2(7891):1271-2. PubMed ID: 4139513
    [No Abstract]   [Full Text] [Related]  

  • 19. Letter: Lysine metabolism in Reye's syndrome.
    Shih VE; Glick TH; Bercu BB
    Lancet; 1974 Jul; 2(7873):163-4. PubMed ID: 4135529
    [No Abstract]   [Full Text] [Related]  

  • 20. Metabolic disorders mimicking Reye's syndrome.
    Chang PF; Huang SF; Hwu WL; Hou JW; Ni YH; Chang MH
    J Formos Med Assoc; 2000 Apr; 99(4):295-9. PubMed ID: 10870312
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.