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5. Chiral compounds as indicators of inherited metabolic disease. Simultaneous stereodifferentiation of lactic-, 2-hydroxyglutaric- and glyceric acid by enantioselective cGC. Kaunzinger A; Rechner A; Beck T; Mosandl A; Sewell AC; Böhles H Enantiomer; 1996; 1(3):177-82. PubMed ID: 9676282 [TBL] [Abstract][Full Text] [Related]
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7. Low molecular weight organic acids in the urine of the newborn. Gregersen N; Ingerslev J; Rasmussen K Acta Paediatr Scand; 1977 Jan; 66(1):85-9. PubMed ID: 831385 [TBL] [Abstract][Full Text] [Related]
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11. Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania. Morton DH; Bennett MJ; Seargeant LE; Nichter CA; Kelley RI Am J Med Genet; 1991 Oct; 41(1):89-95. PubMed ID: 1951469 [TBL] [Abstract][Full Text] [Related]
12. Urinary organic acids: isolation and quantification for routine metabolic screening. Greter J; Jacobson CE Clin Chem; 1987 Apr; 33(4):473-80. PubMed ID: 3829377 [TBL] [Abstract][Full Text] [Related]
13. Identification and quantitation of urinary dicarboxylic acids as their dicyclohexyl esters in disease states by gas chromatography mass spectrometry. Norman EJ; Berry HK; Denton MD Biomed Mass Spectrom; 1979 Dec; 6(12):546-53. PubMed ID: 526567 [TBL] [Abstract][Full Text] [Related]
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18. Organic acids in urine from human newborns. Björkman L; McLean C; Steen G Clin Chem; 1976 Jan; 22(1):49-52. PubMed ID: 1245060 [TBL] [Abstract][Full Text] [Related]
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