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2. [Implementation of a screening program for some hereditary metabolic diseases in the Autonomic Region of the Aosta Valley]. Lanza I; Barbero PC; Anzelmo G; Machado E; Verri B Minerva Pediatr; 1975 Feb; 27(3):139-47. PubMed ID: 1226190 [No Abstract] [Full Text] [Related]
3. Screening program for genetic/metabolic disorders. J Iowa Med Soc; 1980 Feb; 70(2):66, 69, 72. PubMed ID: 7354225 [No Abstract] [Full Text] [Related]
4. Newborn screening for metabolic disorders. DiSalvo AF J S C Med Assoc; 1987 May; 83(5):276-7. PubMed ID: 3474476 [No Abstract] [Full Text] [Related]
5. [Metabolic diseases--screening of newborn infants]. Søvik O Tidsskr Nor Laegeforen; 1995 Feb; 115(5):582-3. PubMed ID: 7900108 [No Abstract] [Full Text] [Related]
6. [Mass screening of inborn errors of metabolism]. Ooura T Nihon Rinsho; 1978 May; Suppl():1328-9. PubMed ID: 691340 [No Abstract] [Full Text] [Related]
7. [Problems in the diagnosis of hereditary metabolic defects in pediatric neurology]. Krasnopol'skaia KD; Lebedeva TV; Odinokova ON; Iakovlev SA Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(10):1458-61. PubMed ID: 6438970 [TBL] [Abstract][Full Text] [Related]
9. DELAWARE'S PHENYLKETONURIA EARLY DETECTION AND SCREENING PROGRAM. ALVAREZ DA Del Med J; 1963 Sep; 35():232-4. PubMed ID: 14048873 [No Abstract] [Full Text] [Related]
10. [Possible interfering factors in the screening of newborn infants for inborn errors of metabolism and measures for their prevention]. Mathias D; Bickel H Monatsschr Kinderheilkd; 1987 May; 135(5):282-4. PubMed ID: 3614225 [TBL] [Abstract][Full Text] [Related]
12. Neonatal screening for congenital disorders. Gudat JC; Maclaren NK J Fla Med Assoc; 1980 Feb; 67(2):137-42. PubMed ID: 7359105 [No Abstract] [Full Text] [Related]
13. [Clinical research in the university: prototype based on the discovery, treatment and prevention of hereditary metabolic disease]. Velázquez A Bol Estud Med Biol; 1983; 32(7-8 Suppl 1):309-17. PubMed ID: 6399686 [No Abstract] [Full Text] [Related]
14. [Neonatal screening--present and future]. Miyai K Rinsho Byori; 1986 Jun; 34(6):658-65. PubMed ID: 3747207 [No Abstract] [Full Text] [Related]
15. [Use of dried samples of biological material in screening for hereditary metabolic defects]. Iakovenko LP; Bialik MA; Krasnopol'skaia KD Lab Delo; 1983; (10):16-9. PubMed ID: 6196522 [No Abstract] [Full Text] [Related]
17. Inborn errors of metabolism at the turn of the millennium. Barić I; Fumić K; Hoffmann GF Croat Med J; 2001 Aug; 42(4):379-83. PubMed ID: 11471189 [TBL] [Abstract][Full Text] [Related]
18. Expanded newborn screening for genetic and metabolic disorders: modeling costs and outcomes. Hubbard HB Nurs Econ; 2007; 25(6):345-52. PubMed ID: 18240836 [TBL] [Abstract][Full Text] [Related]
19. Letter: Screening for hereditary metabolic disease. Hardwick DF; Applegarth DA; Davidson AG; Israels S Can Med Assoc J; 1975 Mar; 112(6):678-9. PubMed ID: 1122433 [No Abstract] [Full Text] [Related]