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3. [Neonatal diagnosis of hereditary metabolic diseases]. Lambotte C Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974 [No Abstract] [Full Text] [Related]
4. [Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease]. Menne F; Otte HJ; Krüger M; Winterhoff D MMW Munch Med Wochenschr; 1979 Jun; 121(25):833-4. PubMed ID: 111089 [No Abstract] [Full Text] [Related]
5. 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]
10. Newborn screening: the role of the obstetrician. Larsson A; Therrell BL Clin Obstet Gynecol; 2002 Sep; 45(3):697-710; discussion 730-2. PubMed ID: 12370609 [No Abstract] [Full Text] [Related]
11. Austria newborn screening programme for inborn errors of metabolism. Thalhammer O Acta Univ Carol Med Monogr; 1973; 56():79-82. PubMed ID: 4791784 [No Abstract] [Full Text] [Related]
12. Neonatal screening of phenylketonuria and congenital hypothyroidism in China. Fan GX; Jun Y; Rui-guan C Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():17-9. PubMed ID: 11400761 [TBL] [Abstract][Full Text] [Related]
14. [Early diagnosis of mental deficiency caused by metabolic diseases in children]. Bickel H Landarzt; 1965 May; 41(13):548-9. PubMed ID: 5827014 [No Abstract] [Full Text] [Related]
15. [Screening of newborn infants for phenylketonuria and trends in the therapy of patients with phenylketonuria]. Országos C; Gyermekegészségügyi I Orv Hetil; 1975 Oct; 116(42):2485-6. PubMed ID: 1187128 [No Abstract] [Full Text] [Related]
16. Neonatal hypothyroidism, phenylketonuria and galactosemia screening in metropolitan Shanghai. Chen RG; Sun M; Ni YY; Pan XS; Chen JZ; Zhang YF; Liu H; Zhang MH; Xu HZ; Wu YL Chin Med J (Engl); 1984 Jan; 97(1):61-5. PubMed ID: 6428834 [No Abstract] [Full Text] [Related]
17. Newborn screening for certain treatable inborn errors of metabolism in Alexandria. Ismail SR; Abdel-Rahim N; Hashishe MM; Abdallah EM J Egypt Public Health Assoc; 1996; 71(5-6):495-520. PubMed ID: 17214193 [TBL] [Abstract][Full Text] [Related]
18. [Screening for congenital hypothyroidism, phenylketonuria, galactosemia and biotinidase deficiency in a sample of mentally retarded patients in the city of Havana]. Marrero-González N; Portuondo-Sao M; Lardoeyt-Ferrer R; Tassé-Vila D; Lantigua-Cruz A Rev Neurol; 2003 May 16-31; 36(10):913-6. PubMed ID: 12766862 [TBL] [Abstract][Full Text] [Related]
19. [Prenatal and postnatal diagnosis (trisomy 21, phenylketonuria, hypothyroidism). Methods, indications, legal and ethical aspects]. Vidailhet M Rev Prat; 1994 May; 44(9):1241-8. PubMed ID: 7939350 [No Abstract] [Full Text] [Related]
20. Army experience with certain infant metabolic disorders. Kiel FW Mil Med; 1979 Jul; 144(7):452-5. PubMed ID: 116148 [No Abstract] [Full Text] [Related] [Next] [New Search]