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4. Comparison between amino acids and orotic acid analysis in the detection of urea cycle disorders in the Quebec Urinary Screening Program. Lemieux B; Auray-Blais C; Giguère R Adv Exp Med Biol; 1982; 153():321-9. PubMed ID: 7164907 [No Abstract] [Full Text] [Related]
5. Early detection of phenylketonuria and other aminoacidopathies in a large city using plasma chromatography. Raine DN Arch Dis Child; 1971 Dec; 46(250):885. PubMed ID: 5129211 [No Abstract] [Full Text] [Related]
7. Management of hyperphenylalaninaemia (HPA) in Northern Ireland. Carson NA Arch Dis Child; 1971 Dec; 46(250):885-6. PubMed ID: 5129213 [No Abstract] [Full Text] [Related]
8. Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study. Humangenetik; 1975 Dec; 30(4):273-86. PubMed ID: 1218857 [No Abstract] [Full Text] [Related]
9. [Screening for hyperphenylalaninemia and hypertyrosinemia in the newborn]. Dhondt JL; Farriaux JP Arch Fr Pediatr; 1977 May; 34(5):474-5. PubMed ID: 889411 [No Abstract] [Full Text] [Related]
11. Aminoacid excretion in infancy and early childhood. A survey of 100,000 infants. Turner B; Brown DA Med J Aust; 1970 Jan; 1(1):11-4. PubMed ID: 5436523 [No Abstract] [Full Text] [Related]
12. The incidence of urea cycle disorders. Summar ML; Koelker S; Freedenberg D; Le Mons C; Haberle J; Lee HS; Kirmse B; ; Mol Genet Metab; 2013; 110(1-2):179-80. PubMed ID: 23972786 [TBL] [Abstract][Full Text] [Related]
14. A prospective community survey for aminoacidaemias. Komrower GM; Griffiths MJ; Fowler B; Lambert AM Proc R Soc Med; 1968 Mar; 61(3):294-6. PubMed ID: 5689917 [No Abstract] [Full Text] [Related]
15. A new method for screening of hyperammonemia. Tada K; Tateda H; Metoki K Adv Exp Med Biol; 1982; 153():19-27. PubMed ID: 7164897 [No Abstract] [Full Text] [Related]
16. Screening tests for argininosuccinic aciduria, orotic aciduria, and other inherited enzyme deficiencies using dried blood specimens. Murphey WH; Patchen L; Guthrie R Biochem Genet; 1972 Feb; 6(1):51-9. PubMed ID: 4199795 [No Abstract] [Full Text] [Related]
17. Experience with a screening service, using the Guthrie test, in the north-west and north-east metropolitan regions. Clayton BE Arch Dis Child; 1971 Dec; 46(250):881-2. PubMed ID: 5129203 [No Abstract] [Full Text] [Related]
18. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience. Karam PE; Habbal MZ; Mikati MA; Zaatari GE; Cortas NK; Daher RT Clin Biochem; 2013 Dec; 46(18):1787-92. PubMed ID: 23994778 [TBL] [Abstract][Full Text] [Related]
19. Chromatographic screening of 70,328 neonates for inborn errors of amino acid metabolism. Méhes K; Juhász E; Ruszinkó V Acta Paediatr Hung; 1985; 26(2):147-9. PubMed ID: 4041281 [TBL] [Abstract][Full Text] [Related]
20. Screening for aminoaciduria: a critical evaluation of four techniques and a survey of a mentally retarded population. Tippett PA; Danks DM Aust Paediatr J; 1972 Oct; 8(5):255-63. PubMed ID: 4658964 [No Abstract] [Full Text] [Related] [Next] [New Search]