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31. A guide to screening newborn infants for inborn errors of metabolism. Buist NR; Jhaveri BM J Pediatr; 1973 Mar; 82(3):511-22. PubMed ID: 4266933 [No Abstract] [Full Text] [Related]
32. Rapid screening methods for the detection of inherited and acquired aminoacidopathies. Saifer A Adv Clin Chem; 1971; 14():145-218. PubMed ID: 4109903 [No Abstract] [Full Text] [Related]
33. Diagnosis and treatment: interpreting the positive screening test in the newborn infant. Scriver CR Pediatrics; 1967 May; 39(5):764-8. PubMed ID: 6026878 [No Abstract] [Full Text] [Related]
34. [Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages]. Simková M; Hyánek J; Karger P; Hoza J; Holub J; Viletová H Cesk Pediatr; 1976 Nov; 31(11):619-21. PubMed ID: 1035139 [No Abstract] [Full Text] [Related]
35. Genetic screening of the newborn in Australia. Results for 1978. Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Hill G; Masters P; Tucker RG; Raby J; McFarlane J Med J Aust; 1979 Sep; 2(5):272-3. PubMed ID: 514173 [TBL] [Abstract][Full Text] [Related]
36. Urinary screening tests in the infant and young child. Bradley GM Hum Pathol; 1971 Jun; 2(2):309-20. PubMed ID: 4256386 [No Abstract] [Full Text] [Related]
37. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report]. Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466 [No Abstract] [Full Text] [Related]
38. Mass screening of the newborn for metabolic disease. Woolf LI Arch Dis Child; 1968 Apr; 43(228):137-40. PubMed ID: 5645685 [No Abstract] [Full Text] [Related]
39. Hyperphenylalaninemia syndromes: current status of diagnosis and management. Matsuo N Keio J Med; 1988 Mar; 37(1):1-9. PubMed ID: 3286956 [No Abstract] [Full Text] [Related]