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Journal Abstract Search
121 related items for PubMed ID: 9565984
41. Identification and quantification of intermediates of unsaturated fatty acid metabolism in plasma of patients with fatty acid oxidation disorders. Onkenhout W, Venizelos V, van der Poel PF, van den Heuvel MP, Poorthuis BJ. Clin Chem; 1995 Oct; 41(10):1467-74. PubMed ID: 7586519 [Abstract] [Full Text] [Related]
42. Clinical diagnosis of long-chain acyl-coenzyme A-dehydrogenase deficiency: use of stress and fat-loading tests. Parini R, Garavaglia B, Saudubray JM, Bardelli P, Melotti D, Zecca G, Di Donato S. J Pediatr; 1991 Jul; 119(1 Pt 1):77-80. PubMed ID: 2066862 [No Abstract] [Full Text] [Related]
44. 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 [Abstract] [Full Text] [Related]
46. MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency. Spiekerkoetter U, Sun B, Zytkovicz T, Wanders R, Strauss AW, Wendel U. J Pediatr; 2003 Sep; 143(3):335-42. PubMed ID: 14517516 [Abstract] [Full Text] [Related]
47. [Very-long-chain acyl-CoA dehydrogenase deficiency presenting with recurrent rhabdomyolysis in an adult]. Hamano H, Shinohara Y, Takizawa S, Tokuoka K, Kazahari S, Mandokoro H, Sato A. Rinsho Shinkeigaku; 2003 May; 43(5):253-7. PubMed ID: 12931630 [Abstract] [Full Text] [Related]
48. Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency. Dawson DB, Waber L, Hale DE, Bennett MJ. J Pediatr; 1995 Jan; 126(1):69-71. PubMed ID: 7815229 [Abstract] [Full Text] [Related]