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25. Screening for inborn errors of amino acid metabolism. Wu JT Ann Clin Lab Sci; 1991; 21(2):123-42. PubMed ID: 2029175 [TBL] [Abstract][Full Text] [Related]
26. Problems in screening infants for defects of amino acid metabolism. Jackson SH Clin Biochem; 1973 Mar; 6(1):15-21. PubMed ID: 4121648 [No Abstract] [Full Text] [Related]
27. [Methods of thin-layer chromatography for the identification of aminoaciduria, aminoacidemia and galactosemia]. Bremer HJ; Nützenadel W; Bickel H Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):32-7. PubMed ID: 5408275 [No Abstract] [Full Text] [Related]
28. [Methylmalonic acidemia. A new method of diagnosis]. Rufini S; Ghebregzabher M; Bragetti P; Lato M Minerva Pediatr; 1983 Apr; 35(7):335-9. PubMed ID: 6865877 [No Abstract] [Full Text] [Related]
29. Studies on fluorescamine: Part I--Applications of fluorescamine in forensic toxicological analysis. Nowicki HG J Forensic Sci; 1976 Jan; 21(1):154-62. PubMed ID: 1249547 [TBL] [Abstract][Full Text] [Related]
30. Rapid screening methods for the detection of inherited and acquired aminoacidopathies. Saifer A Adv Clin Chem; 1971; 14():145-218. PubMed ID: 4109903 [No Abstract] [Full Text] [Related]
31. [Methylmalonic aciduria - diagnosis and therapy using as example 2 cases of this genetic metabolic disorder]. Lubs H; Seidlitz G; Pfau E Padiatr Grenzgeb; 1982; 21(4):319-26. PubMed ID: 7177670 [No Abstract] [Full Text] [Related]
32. Cactus alkaloids. XXVII. Use of fluorescamine as a thin-layer chromatographic visualization reagent for alkaloids. Ranieri RL; McLaughlin JL J Chromatogr; 1975 Aug; 111(1):234-7. PubMed ID: 1159001 [No Abstract] [Full Text] [Related]
33. HPLC analysis of amino acids in inborn errors of metabolism. Matteson KJ Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():120-2. PubMed ID: 8629089 [TBL] [Abstract][Full Text] [Related]
34. Sample preparation for chromatography of amino acids. Ryan WL Am J Med Technol; 1973 Feb; 39(2):52-4. PubMed ID: 4701051 [No Abstract] [Full Text] [Related]