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Journal Abstract Search

140 related items for PubMed ID: 4178399

  • 1. Screening method for detection of specific aminoacidemias.
    Szeinberg A, Szeinberg B, Cohen BE.
    Clin Chim Acta; 1969 Jan; 23(1):93-5. PubMed ID: 4178399
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Rapid diagnosis of phenylketonuria and other aminoacidemias by quantitative analysis of amino acids in neonatal blood spots by gas chromatography-mass spectrometry.
    Deng C, Shang C, Hu Y, Zhang X.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2002 Jul 25; 775(1):115-20. PubMed ID: 12101068
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary tyrosinemia. II. Presentation of a system of detection].
    Bélanger M, Saint-Hilaire B.
    Pediatrie; 1973 Jul 25; 28(1):19-22. PubMed ID: 4715464
    [No Abstract] [Full Text] [Related]

  • 5. Quantitative evaluation of thin-layer ion-exchange chromatograms by video-densitometry II. Screening test for amino-acidaemias in blood samples dried on filter paper.
    Pongor S, Kovács J, Dévényi T.
    Acta Biochim Biophys Acad Sci Hung; 1978 Jul 25; 13(3):117-21. PubMed ID: 754443
    [No Abstract] [Full Text] [Related]

  • 6. Rapid screening methods for the detection of inherited and acquired aminoacidopathies.
    Saifer A.
    Adv Clin Chem; 1971 Jul 25; 14():145-218. PubMed ID: 4109903
    [No Abstract] [Full Text] [Related]

  • 7. [Amino acid composition in blood and urine from healthy newborn infants: screening test for the detection of enxymopathies].
    Adrienne S.
    Orv Hetil; 1969 Jun 08; 110(23):1315-20. PubMed ID: 5794637
    [No Abstract] [Full Text] [Related]

  • 8. The assessment of serum amino acids.
    Swallow WH, Carrell RW.
    N Z Med J; 1970 Feb 08; 71(453):85-8. PubMed ID: 5267129
    [No Abstract] [Full Text] [Related]

  • 9. Plasma amino acids: screening, quantitation, and interpretation.
    Scriver CR, Lamm P, Clow CL.
    Am J Clin Nutr; 1971 Jul 08; 24(7):876-90. PubMed ID: 4933289
    [No Abstract] [Full Text] [Related]

  • 10. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism].
    Charpentier C, Lemonnier A.
    Ann Biol Clin (Paris); 1969 Jul 08; 27(5):297-323. PubMed ID: 4897889
    [No Abstract] [Full Text] [Related]

  • 11. [Screening on aminoacid opathies in newborn infants].
    Stoppoloni G, Santinelli R.
    Pediatria (Napoli); 1976 Dec 31; 84(4):604-16. PubMed ID: 1035798
    [No Abstract] [Full Text] [Related]

  • 12. Hypermethioninemia with other hyperaminoacidemias. Studies in infants on high-protein diets.
    Levy HL, Shih VE, Madigan PM, Karolkewicz V, Carr JR, Lum A, Richards AA, Crawford JD, MacCready RA.
    Am J Dis Child; 1969 Jan 31; 117(1):96-103. PubMed ID: 5812761
    [No Abstract] [Full Text] [Related]

  • 13. Thin-layer ion-exchange chromatographic screening test for aminoacidemias in blood samples dried on filter paper.
    Dévényi T, Báti J, Kovács J, Kiss P.
    Acta Biochim Biophys Acad Sci Hung; 1972 Jan 31; 7(3):237-9. PubMed ID: 4672028
    [No Abstract] [Full Text] [Related]

  • 14. Saudi aminoacidemias: a six-year study.
    Subramanyam SB.
    Indian J Pediatr; 1996 Jan 31; 63(5):641-4. PubMed ID: 10830032
    [Abstract] [Full Text] [Related]

  • 15. Results of mass screening for hyperaminoacidemias in the newborn infant.
    Clow C, Scriver CR, Davies E.
    Am J Dis Child; 1969 Jan 31; 117(1):48-53. PubMed ID: 5782532
    [No Abstract] [Full Text] [Related]

  • 16. [Thin layer chromatography studies of capillary blood in newborn infants. Evaluation of utility for mass screening].
    Coradello H.
    Klin Padiatr; 1972 Sep 31; 184(5):358-66. PubMed ID: 4673723
    [No Abstract] [Full Text] [Related]

  • 17. [A system of early screening for inborn errors of metabolism: methods and results for hereditary tyrosinemia].
    Bélanger M, Saint-Hilaire B, Bélanger L.
    Union Med Can; 1973 Feb 31; 102(2):294-302. PubMed ID: 4709460
    [No Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities.
    Wadman SK.
    Acta Univ Carol Med Monogr; 1977 Jun 28; (77 Pt 1):49-69. PubMed ID: 615451
    [No Abstract] [Full Text] [Related]

  • 20. 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]

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