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.
17. Mitochondrial fatty acid oxidation disorders in Thai infants: a report of 3 cases. Wasant P; Matsumoto I; Naylor E; Liammongkolkul S J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S710-9. PubMed ID: 12403251 [TBL] [Abstract][Full Text] [Related]
18. Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis. Matern D; Strauss AW; Hillman SL; Mayatepek E; Millington DS; Trefz FK Pediatr Res; 1999 Jul; 46(1):45-9. PubMed ID: 10400133 [TBL] [Abstract][Full Text] [Related]
19. Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey. Gillingham M; Van Calcar S; Ney D; Wolff J; Harding C J Inherit Metab Dis; 1999 Apr; 22(2):123-31. PubMed ID: 10234607 [TBL] [Abstract][Full Text] [Related]
20. Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Lawlor DP; Kalina RE Am J Ophthalmol; 1997 Jun; 123(6):846-8. PubMed ID: 9535636 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]