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Journal Abstract Search
421 related items for PubMed ID: 4821497
21. [Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests]. Schmid-Rüter E. Fortschr Med; 1978 Jun 22; 96(24):1289-93. PubMed ID: 96002 [Abstract] [Full Text] [Related]
28. The value of screening in paediatrics. Carter RA. J R Coll Physicians Lond; 1976 Jan 13; 10(2):153-60. PubMed ID: 54421 [No Abstract] [Full Text] [Related]
30. [The early recognition of congenital metabolic diseases]. Steuber W. Munch Med Wochenschr; 1971 Mar 26; 113(13):463-7. PubMed ID: 5108281 [No Abstract] [Full Text] [Related]
31. Dietary restriction in inborn errors of amino acid metabolism. Bickel H. Curr Concepts Nutr; 1979 Mar 26; 8():35-53. PubMed ID: 527358 [No Abstract] [Full Text] [Related]
32. Newborn screening programme expanded. Community Pract; 2015 Feb 26; 88(2):5. PubMed ID: 25720200 [No Abstract] [Full Text] [Related]
33. Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria. Antonozzi I, Dominici R, Andreoli M, Monaco F. J Endocrinol Invest; 1980 Feb 26; 3(4):357-63. PubMed ID: 7204885 [Abstract] [Full Text] [Related]
36. Detection of heterozygotes for phenylketonuria and hyperphenylaianinemia by gas-chromatographic analysis of aromatic acid excretion in urine. Koepp P, Hoffman B. Clin Chim Acta; 1975 Feb 08; 58(3):215-21. PubMed ID: 1112063 [No Abstract] [Full Text] [Related]