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Journal Abstract Search
142 related items for PubMed ID: 4121648
1. Problems in screening infants for defects of amino acid metabolism. Jackson SH. Clin Biochem; 1973 Mar; 6(1):15-21. PubMed ID: 4121648 [No Abstract] [Full Text] [Related]
2. Screening for disorders of amino acid metabolism by thin-layer high voltage electrophoresis. Farrelly RO, Watkins WB. Clin Chim Acta; 1968 May; 20(2):291-4. PubMed ID: 4297715 [No Abstract] [Full Text] [Related]
3. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants. Turner B, Brown DA. Med J Aust; 1972 Jan 08; 1(2):62-5. PubMed ID: 5025157 [No Abstract] [Full Text] [Related]
4. Neonatal screening for inborn errors of amino acid metabolism. Levy HL. Clin Endocrinol Metab; 1974 Mar 08; 3(1):153-66. PubMed ID: 4609646 [No Abstract] [Full Text] [Related]
5. A sensitive chromatographic technique for screening of amino acid metabolic defects in the newborn. Lato M, Rufini S, Ghebregzabher M, Ciuffini G, Mezzetti T. Clin Chim Acta; 1974 Jun 28; 53(3):273-80. PubMed ID: 4858769 [No Abstract] [Full Text] [Related]
6. The assessment of serum amino acids. Swallow WH, Carrell RW. N Z Med J; 1970 Feb 28; 71(453):85-8. PubMed ID: 5267129 [No Abstract] [Full Text] [Related]
7. Thin-layer chromatographic screening of amino acids in plasma and urine of newborns. Century B, Vorkink WP, Natelson S. Clin Chem; 1974 Nov 28; 20(11):1446-50. PubMed ID: 4417439 [No Abstract] [Full Text] [Related]
8. High-voltage electrophoresis in urinary amino acid screening. Holmgren G, Jeppson JO, Samuelson G. Scand J Clin Lab Invest; 1970 Dec 28; 26(4):313-8. PubMed ID: 5486398 [No Abstract] [Full Text] [Related]
10. Screening for inborn errors of amino acid metabolism. Wu JT. Ann Clin Lab Sci; 1991 Apr 28; 21(2):123-42. PubMed ID: 2029175 [Abstract] [Full Text] [Related]
11. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia]. Dhondt JL, Cartigny B, Farriaux JP. Ann Biol Clin (Paris); 1974 Apr 28; 32(6):499-506. PubMed ID: 4468743 [No Abstract] [Full Text] [Related]
12. Screening method for detection of specific aminoacidemias. Szeinberg A, Szeinberg B, Cohen BE. Clin Chim Acta; 1969 Jan 28; 23(1):93-5. PubMed ID: 4178399 [No Abstract] [Full Text] [Related]
13. [Systematic detection of hereditary metabolic encephalopathies]. Neimann N, Pierson M, Vidailhet M, Siest G, Badonnel Y, Humbel R, Roos F. Ann Pediatr (Paris); 1968 Oct 02; 15(10):635-41. PubMed ID: 4237831 [No Abstract] [Full Text] [Related]
14. Diagnosis and treatment: interpreting the positive screening test in the newborn infant. Scriver CR. Pediatrics; 1967 May 02; 39(5):764-8. PubMed ID: 6026878 [No Abstract] [Full Text] [Related]
15. Screening tests and chromatography for the detection of inborn errors of metabolism. Stuber A. Clin Chim Acta; 1972 Feb 02; 36(2):309-13. PubMed ID: 5008795 [No Abstract] [Full Text] [Related]
16. A simple screening method for detecting isovalerylglycine in urine patients with isovaleric acidemia. Ando T, Nyhan WL. Clin Chem; 1970 May 02; 16(5):420-2. PubMed ID: 5443766 [No Abstract] [Full Text] [Related]
17. Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose. Vercaemst R, Blaton V, Lievens-Taveirne J, Peeters H. Acta Paediatr Belg; 1973 May 02; 27(5):334-47. PubMed ID: 4779694 [No Abstract] [Full Text] [Related]
18. Evaluation of a simple thin-layer chromatographic screening test for amino acid abnormalities. Berry HK. J Chromatogr; 1971 Apr 07; 56(2):316-20. PubMed ID: 5551913 [No Abstract] [Full Text] [Related]