143 related articles for article (PubMed ID: 8411999)
21. The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiency.
Seakins JW; Rumsby G
J Inherit Metab Dis; 1988; 11 Suppl 2():221-4. PubMed ID: 3141707
[No Abstract] [Full Text] [Related]
22. Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementation.
Duran M; Cleutjens CB; Ketting D; Dorland L; de Klerk JB; van Sprang FJ; Berger R
Pediatr Res; 1992 Jan; 31(1):39-42. PubMed ID: 1594328
[TBL] [Abstract][Full Text] [Related]
23. Profiles in altered metabolism. II--(omega -- 1)-hydroxyacid excretion in a case of episodic hypoglycemia.
Mamer OA; Montgomery JA; Colle E
Biomed Mass Spectrom; 1980 Feb; 7(2):53-7. PubMed ID: 6893290
[TBL] [Abstract][Full Text] [Related]
24. A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome.
Del Valle JA; Garcia MJ; Merinero B; Pérez-Cerdá C; Roman F; Jimenez A; Ugarte M; Martínez-Pardo M; Ludeña C; Camarero C
J Inherit Metab Dis; 1984; 7(2):62-4. PubMed ID: 6434827
[TBL] [Abstract][Full Text] [Related]
25. Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency.
Heales SJ; Thompson GN; Massoud AF; Rahman S; Halliday D; Leonard JV
J Inherit Metab Dis; 1994; 17(1):74-80. PubMed ID: 8051939
[TBL] [Abstract][Full Text] [Related]
26. Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain acyl-CoA dehydrogenase.
Niezen-Koning KE; Wanders RJ; Nagel GT; Sewell AC; Heymans HS
Clin Chim Acta; 1994 Sep; 229(1-2):99-106. PubMed ID: 7988059
[TBL] [Abstract][Full Text] [Related]
27. Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.
Albers S; Levy HL; Irons M; Strauss AW; Marsden D
J Inherit Metab Dis; 2001 Jun; 24(3):417-8. PubMed ID: 11486912
[No Abstract] [Full Text] [Related]
28. Simple high-performance liquid chromatographic method for the detection of phenylpropionylglycine in urine as a diagnostic tool in inherited medium-chain acyl-coenzyme A dehydrogenase deficiency.
Flath B; Rolinski B; Roscher AA
J Chromatogr B Biomed Sci Appl; 1997 Jun; 694(1):227-32. PubMed ID: 9234867
[TBL] [Abstract][Full Text] [Related]
29. Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiency.
Rinaldo P; O'Shea JJ; Goodman SI; Miller LV; Fennessey PV; Whelan DT; Hill RE; Tanaka K
J Inherit Metab Dis; 1989; 12 Suppl 2():325-8. PubMed ID: 2512435
[No Abstract] [Full Text] [Related]
30. Acylcarnitines in the urine of a patient with medium chain acyl-CoA dehydrogenase (MCAD) deficiency and in normal children.
Schmidt-Sommerfeld E; Penn D; Kerner J; Bieber LL
Prog Clin Biol Res; 1990; 321():403-9. PubMed ID: 2326301
[No Abstract] [Full Text] [Related]
31. Inhibition of a medium chain acyl-CoA synthetase involved in glycine conjugation by carboxylic acids.
Kasuya F; Igarashi K; Fukui M
Biochem Pharmacol; 1996 Nov; 52(10):1643-6. PubMed ID: 8937481
[TBL] [Abstract][Full Text] [Related]
32. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in 2 patients with symptoms of Reye syndrome].
Brus F; Smit GP; Knoester H; Reijngoud DJ
Tijdschr Kindergeneeskd; 1988 Jun; 56(3):132-7. PubMed ID: 3046055
[TBL] [Abstract][Full Text] [Related]
33. Plasma cis-dec-4-enoic acid measured by isotope dilution mass spectrometry; an improved assay to diagnose medium-chain acyl-CoA dehydrogenase deficiency.
Johnson DW; Harrison JR; Norton WA; Poulos A; Robertson EF
J Inherit Metab Dis; 1994; 17(5):554-9. PubMed ID: 7837761
[TBL] [Abstract][Full Text] [Related]
34. Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiency.
Ikeda Y; Hale DE; Keese SM; Coates PM; Tanaka K
Pediatr Res; 1986 Sep; 20(9):843-7. PubMed ID: 3748657
[TBL] [Abstract][Full Text] [Related]
35. Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry.
Clayton PT; Doig M; Ghafari S; Meaney C; Taylor C; Leonard JV; Morris M; Johnson AW
Arch Dis Child; 1998 Aug; 79(2):109-15. PubMed ID: 9797589
[TBL] [Abstract][Full Text] [Related]
36. Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspects.
Matsubara Y; Narisawa K; Tada K
Eur J Pediatr; 1992 Mar; 151(3):154-9. PubMed ID: 1601002
[TBL] [Abstract][Full Text] [Related]
37. Diagnosis of medium chain acyl-CoA dehydrogenase deficiency in the newborn.
Walker V; Mills GA; Radford M
Lancet; 1990 May; 335(8700):1288-9. PubMed ID: 1971365
[No Abstract] [Full Text] [Related]
38. The enzymatic basis for the dehydrogenation of 3-phenylpropionic acid: in vitro reaction of 3-phenylpropionyl-CoA with various acyl-CoA dehydrogenases.
Rinaldo P; O'Shea JJ; Welch RD; Tanaka K
Pediatr Res; 1990 May; 27(5):501-7. PubMed ID: 2345678
[TBL] [Abstract][Full Text] [Related]
39. Delayed diagnosis of fatal medium-chain acyl-CoA dehydrogenase deficiency in a child.
Shetty AK; Craver RD; Harris JA; Schmidt-Sommerfeld E
Pediatr Emerg Care; 1999 Dec; 15(6):399-401. PubMed ID: 10608324
[TBL] [Abstract][Full Text] [Related]
40. Medium-chain acyl-CoA dehydrogenase deficiency.
Egidio RJ; Francis GL; Coates PM; Hale DE; Roesel A
Am Fam Physician; 1989 May; 39(5):221-6. PubMed ID: 2718899
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]