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.
12. Medium-chain acyl-CoA dehydrogenase deficiency presenting in the neonatal period: the first Italian case. Burlina AB; Bennett MJ; Gregersen N; Dalla Barba B; Zacchello F Eur J Pediatr; 1995 Nov; 154(11):940-1. PubMed ID: 8582415 [No Abstract] [Full Text] [Related]
13. Diagnosis of medium chain acyl CoA dehydrogenase deficiency by measurement of cis-4-decenoic acid in dried blood spots. Heales SJ; Leonard JV Clin Chim Acta; 1992 Jul; 209(1-2):61-6. PubMed ID: 1395039 [TBL] [Abstract][Full Text] [Related]
18. Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by oligonucleotide ligation assay. Tuchman M Clin Chem; 1998 Jan; 44(1):10-1. PubMed ID: 9550552 [No Abstract] [Full Text] [Related]
19. Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12. Morris AA; Taylor RW; Lightowlers RN; Aynsley-Green A; Bartlett K; Turnbull DM Hum Mol Genet; 1995 Apr; 4(4):747-9. PubMed ID: 7633427 [No Abstract] [Full Text] [Related]
20. Identification of new medium-chain acylcarnitines present in urine of a patient with medium-chain acyl-CoA dehydrogenase deficiency. Libert R; Van Hoof F; Thillaye M; Vincent MF; Nassogne MC; Stroobant V; de Hoffmann E; Schanck A J Inherit Metab Dis; 1999 Feb; 22(1):9-18. PubMed ID: 10070613 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]