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5. Hyperphenylalaninemias and tyrosinemias. Berry HK Clin Perinatol; 1976 Mar; 3(1):15-40. PubMed ID: 954342 [No Abstract] [Full Text] [Related]
6. 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]
7. 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]
8. The dangers of a successful PKU program. Gerald PS Pediatrics; 1967 Mar; 39(3):325-6. PubMed ID: 6018963 [No Abstract] [Full Text] [Related]
9. Neonatal screening for phenylketonuria. II. Age dependence of initial phenylalanine in infants with PKU. Holtzman NA; Mellits ED; Kallman CH Pediatrics; 1974 Mar; 53(3):353-7. PubMed ID: 4815254 [No Abstract] [Full Text] [Related]
10. [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. Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe. Wachtel U Hum Nutr Appl Nutr; 1986; 40 Suppl 1():61-9. PubMed ID: 3528074 [TBL] [Abstract][Full Text] [Related]
12. The place of large-scale screening in the prevention of hereditary diseases. Phenylketonuria. Szeinberg A; Cohen BE Isr J Med Sci; 1973; 9(9):1319-22. PubMed ID: 4775112 [No Abstract] [Full Text] [Related]
13. [Detection of inborm errors in the metabolism of amino-acids, organic acids and carbohydrates in a children's hospital of Mexico City]. Villarreal ML; Velázquez A; Carnevale A; del Castillo V; Márquez Solís E Bol Med Hosp Infant Mex; 1978; 35(2):205-15. PubMed ID: 626648 [No Abstract] [Full Text] [Related]
14. [Laboratory examinations for inborn errors of metabolism]. Kawamura M Rinsho Byori; 1986 Feb; 34(2):133-5. PubMed ID: 3702083 [No Abstract] [Full Text] [Related]
15. 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]
17. 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]
18. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood. Güttler F Acta Paediatr Scand Suppl; 1980; 280():1-80. PubMed ID: 7006308 [No Abstract] [Full Text] [Related]
19. [A system of early screening for inborn errors of metabolism: methods and results for hereditary tyrosinemia]. Bélanger M; Saint-Hilaire B; Bélanger L Union Med Can; 1973 Feb; 102(2):294-302. PubMed ID: 4709460 [No Abstract] [Full Text] [Related]
20. [The frequency of some oligophrenias due to metabolic diseases in the grand-duchy of Luxembourg]. Kutter D; Metz H Schweiz Arch Neurol Neurochir Psychiatr; 1968; 101(2):369-82. PubMed ID: 5705003 [No Abstract] [Full Text] [Related] [Next] [New Search]