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Journal Abstract Search

116 related items for PubMed ID: 9329424

  • 1. Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt management.
    Sluysmans T, Tuerlinckx D, Hubinont C, Verellen-Dumoulin C, Brivet M, Vianey-Saban C.
    J Pediatr; 1997 Sep; 131(3):444-6. PubMed ID: 9329424
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  • 6. 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; 118(3):1065-9. PubMed ID: 16950999
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  • 8. Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.
    Hale DE, Batshaw ML, Coates PM, Frerman FE, Goodman SI, Singh I, Stanley CA.
    Pediatr Res; 1985 Jul; 19(7):666-71. PubMed ID: 4022672
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  • 9. Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.
    Bonnet D, Martin D, Pascale De Lonlay, Villain E, Jouvet P, Rabier D, Brivet M, Saudubray JM.
    Circulation; 1999 Nov 30; 100(22):2248-53. PubMed ID: 10577999
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  • 10. [Carnitine deficiency in inborn errors of metabolism].
    Sela BA, Lerman-Sagie T, Berkovitz M.
    Harefuah; 1997 Nov 16; 133(10):419-23, 504. PubMed ID: 9418309
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  • 14. 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 16; 19(7):671-6. PubMed ID: 4022673
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  • 15. Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria.
    Minetti C, Garavaglia B, Bado M, Invernizzi F, Bruno C, Rimoldi M, Pons R, Taroni F, Cordone G.
    Neuromuscul Disord; 1998 Feb 16; 8(1):3-6. PubMed ID: 9565984
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  • 17. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency.
    Straussberg R, Harel L, Varsano I, Elpeleg ON, Shamir R, Amir J.
    Pediatrics; 1997 Jun 16; 99(6):894-6. PubMed ID: 9164788
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  • 18. Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.
    Wood JC, Magera MJ, Rinaldo P, Seashore MR, Strauss AW, Friedman A.
    Pediatrics; 2001 Jul 16; 108(1):E19. PubMed ID: 11433098
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  • 20. 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 16; 17(11):877-84. PubMed ID: 6646897
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