These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
76 related articles for article (PubMed ID: 4636582)
1. [Economics of prevention and therapy as shown on the example of phenylketonuria]. Cobet G; Lachmann B; Matthias M Z Arztl Fortbild (Jena); 1972 Aug; 66(16):821-7. PubMed ID: 4636582 [No Abstract] [Full Text] [Related]
3. [Treatment of phenylketonuria. Principles, management and importance of a phenylalanine-free protein hydrolysate]. Boisse J; Saudubray JM; Cathy T; Mozziconacci P Ann Pediatr (Paris); 1971 Feb; 18(2):109-17. PubMed ID: 5549952 [No Abstract] [Full Text] [Related]
4. 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]
9. [On the treatment of phenylketonuria with a low-phenylalanine protein hydrolysate produced by VEB Berlin-Chemie]. Cobet G; Hübschmann K Dtsch Gesundheitsw; 1966 Jun; 21(22):1018-24. PubMed ID: 5973617 [No Abstract] [Full Text] [Related]
11. American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism. Pediatrics; 1982 Jan; 69(1):104-6. PubMed ID: 7054742 [No Abstract] [Full Text] [Related]
12. [Phenylketonuria screening tests in Hungary]. Szabó L; Havass Z; Soltysiak J; Boda D Orv Hetil; 1974 Mar; 115(9):498-504. PubMed ID: 4815454 [No Abstract] [Full Text] [Related]
13. Screening tests for phenylketonuria. Br Med J; 1968 Mar; 1(5593):656-7. PubMed ID: 5640642 [No Abstract] [Full Text] [Related]
17. Screening program for early detection of phenylketonuria in the newborn in Israel. Cohen BE; Szeinberg A; Peled I; Szeinberg B; Bar-Or R Isr J Med Sci; 1966; 2(2):156-64. PubMed ID: 5912550 [No Abstract] [Full Text] [Related]
19. [Phenylketonuria undiagnosed, unrecognizable and neglected. Review of failures in diagnosis, therapy, and prevention of hereditary disorders of phenylalanine]. Hyánek J; Kubík M; Simková M; Zeman J; Houst'ková H Cesk Pediatr; 1987 Mar; 42(3):134-8. PubMed ID: 3581266 [No Abstract] [Full Text] [Related]
20. The newborn phenylketonuria screening program in Ontario. Can Med Assoc J; 1969 Aug; 101(4):185-90. PubMed ID: 5811698 [No Abstract] [Full Text] [Related] [Next] [New Search]