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6. Screening for inborn errors of amino acid metabolism. Wu JT. Ann Clin Lab Sci; 1991; 21(2):123-42. PubMed ID: 2029175 [Abstract] [Full Text] [Related]
7. Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose. Vercaemst R, Blaton V, Lievens-Taveirne J, Peeters H. Acta Paediatr Belg; 1973; 27(5):334-47. PubMed ID: 4779694 [No Abstract] [Full Text] [Related]
8. [Multiple screening test for the detection of inborn errors of metabolism : experiment of mass-screening test with ultra-micro amino acid analysis method in dried blood spot (author's transl)]. Sumi K, Konishi K, Shimizu S, Mimura K, Uemura I, Matsuoka A. Rinsho Byori; 1978 Jun; 26(6):532-6. PubMed ID: 691784 [No Abstract] [Full Text] [Related]
10. [Hereditary tyrosinemia. II. Presentation of a system of detection]. Bélanger M, Saint-Hilaire B. Pediatrie; 1973 Jun; 28(1):19-22. PubMed ID: 4715464 [No Abstract] [Full Text] [Related]
11. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities. Wadman SK. Acta Univ Carol Med Monogr; 1977 Jun; (77 Pt 1):49-69. PubMed ID: 615451 [No Abstract] [Full Text] [Related]
14. [Personal experience in the clinical use of free amino acids in the blood and urine]. Borota J, Velisavljev M, Jojić M. Med Pregl; 1984 Jun; 37(9-10):387-91. PubMed ID: 6530984 [No Abstract] [Full Text] [Related]
16. Amino acid screening of mentally defective patients by high voltage electrophoresis. Meyer JS, Wood MJ. Mo Med; 1972 Feb; 69(2):112-6. PubMed ID: 5058792 [No Abstract] [Full Text] [Related]