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Journal Abstract Search

314 related items for PubMed ID: 3786030

  • 1. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
    Duran M, Hofkamp M, Rhead WJ, Saudubray JM, Wadman SK.
    Pediatrics; 1986 Dec; 78(6):1052-7. PubMed ID: 3786030
    [Abstract] [Full Text] [Related]

  • 2. Medium chain acyl-coenzyme A dehydrogenase deficiency.
    Bennett MJ, Hale DE.
    N J Med; 1992 Sep; 89(9):675-8. PubMed ID: 1436730
    [Abstract] [Full Text] [Related]

  • 3. Diagnosis of mitochondrial fatty acid oxidation defects.
    Duran M, Bruinvis L, Ketting D, Dorland L.
    Padiatr Padol; 1993 Sep; 28(1):19-25. PubMed ID: 8446424
    [Abstract] [Full Text] [Related]

  • 4. Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation.
    Saudubray JM, Coudé FX, Demaugre F, Johnson C, Gibson KM, Nyhan WL.
    Pediatr Res; 1982 Oct; 16(10):877-81. PubMed ID: 7145511
    [Abstract] [Full Text] [Related]

  • 5. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.
    Coates PM, Hale DE, Stanley CA, Corkey BE, Cortner JA.
    Pediatr Res; 1985 Jul; 19(7):671-6. PubMed ID: 4022673
    [Abstract] [Full Text] [Related]

  • 6. Medium chain acyl-coenzyme A dehydrogenase deficiency and SIDS.
    Hegyi T, Ostfeld B, Gardner K.
    N J Med; 1992 May; 89(5):385-92. PubMed ID: 1635678
    [Abstract] [Full Text] [Related]

  • 7. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA.
    Adv Pediatr; 1987 May; 34():59-88. PubMed ID: 3318304
    [Abstract] [Full Text] [Related]

  • 8. Heat stress deteriorates mitochondrial beta-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid beta-oxidation disorders.
    Li H, Fukuda S, Hasegawa Y, Purevsuren J, Kobayashi H, Mushimoto Y, Yamaguchi S.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2010 Jun 15; 878(20):1669-72. PubMed ID: 20207594
    [Abstract] [Full Text] [Related]

  • 9. Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency.
    Taubman B, Hale DE, Kelley RI.
    Pediatrics; 1987 Mar 15; 79(3):382-5. PubMed ID: 3822638
    [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 15; 107(3):397-404. PubMed ID: 4032135
    [Abstract] [Full Text] [Related]

  • 11. Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant death.
    Pollitt RJ.
    Padiatr Padol; 1993 Sep 15; 28(1):13-7. PubMed ID: 8446423
    [Abstract] [Full Text] [Related]

  • 12. Medium-chain acyl-CoA dehydrogenase deficiency.
    Egidio RJ, Francis GL, Coates PM, Hale DE, Roesel A.
    Am Fam Physician; 1989 May 15; 39(5):221-6. PubMed ID: 2718899
    [Abstract] [Full Text] [Related]

  • 13. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels.
    Stanley CA, Hale DE, Coates PM, Hall CL, Corkey BE, Yang W, Kelley RI, Gonzales EL, Williamson JR, Baker L.
    Pediatr Res; 1983 Nov 15; 17(11):877-84. PubMed ID: 6646897
    [Abstract] [Full Text] [Related]

  • 14. In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: limited diagnostic use of 1-13C fatty acid breath test using bolus technique.
    Jakobs C, Kneer J, Martin D, Boulloche J, Brivet M, Poll-The BT, Saudubray JM.
    Eur J Pediatr; 1997 Aug 15; 156 Suppl 1():S78-82. PubMed ID: 9266222
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 16(10):861-8. PubMed ID: 7145508
    [Abstract] [Full Text] [Related]

  • 16. Reye syndrome and reye-like syndrome.
    Gosalakkal JA, Kamoji V.
    Pediatr Neurol; 2008 Sep 15; 39(3):198-200. PubMed ID: 18725066
    [Abstract] [Full Text] [Related]

  • 17. Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.
    Reichmann H, Scheel H, Bier B, Ketelsen UP, Zabransky S.
    Ann Neurol; 1992 Jan 15; 31(1):107-9. PubMed ID: 1311909
    [Abstract] [Full Text] [Related]

  • 18. Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.
    Gregersen N, Andresen BS, Corydon MJ, Corydon TJ, Olsen RK, Bolund L, Bross P.
    Hum Mutat; 2001 Sep 15; 18(3):169-89. PubMed ID: 11524729
    [Abstract] [Full Text] [Related]

  • 19. Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels.
    Liebig M, Schymik I, Mueller M, Wendel U, Mayatepek E, Ruiter J, Strauss AW, Wanders RJ, Spiekerkoetter U.
    Pediatrics; 2006 Sep 15; 118(3):1065-9. PubMed ID: 16950999
    [Abstract] [Full Text] [Related]

  • 20. [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 15; 39(8):661-8. PubMed ID: 6535973
    [Abstract] [Full Text] [Related]

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