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6. [Mass screening of genetic metabolic abnormalities with special reference to amino acid metabolism disorders, using chemical methods]. Lubs H, Knapp A. Z Arztl Fortbild (Jena); 1970 May 15; 64(10):516-9. PubMed ID: 5520559 [No Abstract] [Full Text] [Related]
10. Early detection of inborn errors of metabolism in Poland. Bozkowa K, Cabalska B, Duczynska N, Grodzka Z, Lenartowska I, Helwich E. Acta Anthropogenet; 1983 Feb 15; 7(4):373-81. PubMed ID: 6680316 [Abstract] [Full Text] [Related]
11. Screening urine of 3-week-old newborns: lack of association between sudden infant death syndrome and some metabolic disorders. Lemieux B, Giguere R, Cyr D, Shapcott D, McCann M, Tuchman M. Pediatrics; 1993 May 15; 91(5):986-8. PubMed ID: 8474821 [No Abstract] [Full Text] [Related]
12. Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria. Coulombe JT, Shih VE, Levy HL. Pediatrics; 1981 Jan 15; 67(1):26-31. PubMed ID: 7243433 [Abstract] [Full Text] [Related]
13. [Screening for congenital metabolic disorders]. Knapp A, Machill G. Kinderarztl Prax; 1974 Jun 15; 42(6):270-7. PubMed ID: 4610264 [No Abstract] [Full Text] [Related]
14. Massachusetts Metabolic Disorders Screening Program: III. Sarcosinemia. Levy HL, Coulombe JT, Benjamin R. Pediatrics; 1984 Oct 15; 74(4):509-13. PubMed ID: 6207480 [Abstract] [Full Text] [Related]
16. Results of 10 years of screening of newborn infants for inherited metabolic diseases in the province of Limburg (Belgium). Greven-Brauns G, Mulkens E. Arch Belg Med Soc; 1979 Oct 15; 37(8):516-9. PubMed ID: 550724 [No Abstract] [Full Text] [Related]
17. [Detection of hereditary metabolic diseases in Quebec]. Grenier A, Laberge C. Union Med Can; 1974 Mar 15; 103(3):453-6. PubMed ID: 4820873 [No Abstract] [Full Text] [Related]