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8. The excretion of C6-C10-dicarboxylic acids in the urine of newborn infants during starvation. Evidence for omega-oxidation of fatty acids in the newborn. Gregersen N; Ingerslev J Acta Paediatr Scand; 1979 Sep; 68(5):677-81. PubMed ID: 525335 [TBL] [Abstract][Full Text] [Related]
9. Methylmalonic aciduria and propionic acidaemia studied by proton nuclear magnetic resonance spectroscopy. Iles RA; Chalmers RA; Hind AJ Clin Chim Acta; 1986 Dec; 161(2):173-89. PubMed ID: 3802528 [TBL] [Abstract][Full Text] [Related]
10. Quantitation of methylmalonic acid and other dicarboxylic acids in normal serum and urine using capillary gas chromatography-mass spectrometry. Marcell PD; Stabler SP; Podell ER; Allen RH Anal Biochem; 1985 Oct; 150(1):58-66. PubMed ID: 4083484 [TBL] [Abstract][Full Text] [Related]
11. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects. Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508 [TBL] [Abstract][Full Text] [Related]
12. Formation and degradation of dicarboxylic acids in relation to alterations in fatty acid oxidation in rats. Mortensen PB Biochim Biophys Acta; 1992 Feb; 1124(1):71-9. PubMed ID: 1543729 [TBL] [Abstract][Full Text] [Related]
13. The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic rats. Mortensen PB; Gregersen N Biochim Biophys Acta; 1982 Mar; 710(3):477-84. PubMed ID: 7074126 [TBL] [Abstract][Full Text] [Related]
14. Microdetermination of methylmalonic acid and other short chain dicarboxylic acids by gas chromatography: use in prenatal diagnosis of methylmalonic acidemia and in studies of isovaleric acidemia. Nakamura E; Rosenberg LE; Tanaka K Clin Chim Acta; 1976 Apr; 68(2):127-40. PubMed ID: 1261058 [TBL] [Abstract][Full Text] [Related]
15. [Application of gas chromatography-mass spectrometry analysis on urine filter paper in the high-risk screening and diagnosis of inherited metabolic diseases]. Luo XP; Wang MT; Wei H; Liang Y; Wang HW; Lin HH; Dong YS; Liu WJ; Fang JM; Ning Q Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):245-8. PubMed ID: 14754523 [TBL] [Abstract][Full Text] [Related]
16. The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic rats. Mortensen PB; Gregersen N Biochim Biophys Acta; 1981 Dec; 666(3):394-404. PubMed ID: 6798996 [TBL] [Abstract][Full Text] [Related]
17. Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiency. Di Donato S; Rimoldi M; Garavaglia B; Uziel G Clin Chim Acta; 1984 May; 139(1):13-21. PubMed ID: 6723070 [TBL] [Abstract][Full Text] [Related]
18. C6--C10-dicarboxylic aciduria in starved, fat-fed and diabetic rats receiving decanoic acid or medium-chain triacylglycerol. An in vivo measure of the rate of beta-oxidation of fatty acids. Mortensen PB Biochim Biophys Acta; 1981 May; 664(2):349-55. PubMed ID: 7248330 [TBL] [Abstract][Full Text] [Related]
19. N-Dicarboxylmonoglycines: excretion in dicarboxylic acidurias and mode of formation. Grøn IH; Gregersen N; Rasmussen K J Inherit Metab Dis; 1978; 1(3):109-10. PubMed ID: 116078 [No Abstract] [Full Text] [Related]
20. Gender differences in medium-chain dicarboxylic aciduria in alcoholic men and women. Ma X; Baraona E; Goozner BG; Lieber CS Am J Med; 1999 Jan; 106(1):70-5. PubMed ID: 10320120 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]