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108 related items for PubMed ID: 6818241
21. Family with intermittent maple syrup urine disease. Valman HB, Patrick AD, Seakins JW, Platt JW, Gompertz D. Arch Dis Child; 1973 Mar; 48(3):225-8. PubMed ID: 4693464 [Abstract] [Full Text] [Related]
22. Application of glass capillary-column gas chromatography-mass spectrometry to the studies of human diseases. Jellum E, Storseth P, Alexander J, Helland P, Stokke O, Teig E. J Chromatogr; 1976 Nov 03; 126():487-93. PubMed ID: 789388 [Abstract] [Full Text] [Related]
24. A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria. Freeto S, Mason D, Chen J, Scott RH, Narayan SB, Bennett MJ. Ann Clin Biochem; 2007 Sep 03; 44(Pt 5):474-81. PubMed ID: 17761035 [Abstract] [Full Text] [Related]
25. The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine disease. Snyderman SE, Goldstein F, Sansaricq C, Norton PM. Pediatr Res; 1984 Sep 03; 18(9):851-3. PubMed ID: 6483508 [Abstract] [Full Text] [Related]
27. Keto acid profiling analysis as ethoxime/tert-butyldimethylsilyl derivatives by gas chromatography-mass spectrometry. Nguyen DT, Lee G, Paik MJ. J Chromatogr B Analyt Technol Biomed Life Sci; 2013 Jan 15; 913-914():48-54. PubMed ID: 23270938 [Abstract] [Full Text] [Related]
32. Clinical and biochemical observations on an apparently nonfatal variant of branched-chain ketoaciduria (maple syrup urine disease). MORRIS MD, LEWIS BD, DOOLAN PD, HARPER HA. Pediatrics; 1961 Dec 15; 28():918-23. PubMed ID: 14476272 [No Abstract] [Full Text] [Related]
33. O-trimethylsilylquinoxalinol derivatives of aromatic alpha-keto acids. Mass spectra and quantitative gas chromatography. Langenbeck U, Mench-Hoinowski A, Dieckmann KP, Möhring HU, Petersen M. J Chromatogr; 1978 Mar 01; 145(2):185-93. PubMed ID: 649713 [Abstract] [Full Text] [Related]