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Journal Abstract Search

185 related items for PubMed ID: 4417439

  • 1. Thin-layer chromatographic screening of amino acids in plasma and urine of newborns.
    Century B, Vorkink WP, Natelson S.
    Clin Chem; 1974 Nov; 20(11):1446-50. PubMed ID: 4417439
    [No Abstract] [Full Text] [Related]

  • 2. A survey of inborn errors of amino acid metabolism and transport in man.
    Wellner D, Meister A.
    Annu Rev Biochem; 1981 Nov; 50():911-68. PubMed ID: 6791581
    [No Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [The inborn errors of metabolism of amino acids].
    Tomaszewski L.
    Postepy Biochem; 1973 Mar; 19(1):91-122. PubMed ID: 4697972
    [No Abstract] [Full Text] [Related]

  • 5. A simple screening method for detecting isovalerylglycine in urine patients with isovaleric acidemia.
    Ando T, Nyhan WL.
    Clin Chem; 1970 May; 16(5):420-2. PubMed ID: 5443766
    [No Abstract] [Full Text] [Related]

  • 6. [Diagnostic methods for the detection of amino acid metabolism disorders].
    Lutz P.
    Monatsschr Kinderheilkd (1902); 1973 May; 121(5):184-9. PubMed ID: 4197345
    [No Abstract] [Full Text] [Related]

  • 7. 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; 27(5):334-47. PubMed ID: 4779694
    [No Abstract] [Full Text] [Related]

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

  • 9. 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]

  • 10. [Amino acid metabolism pathology in the convulsive syndrome in young children].
    Alimov IIu, Iur'eva EA, Marchenko ZM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1972 Jun 28; 72(10):1497-500. PubMed ID: 4660427
    [No Abstract] [Full Text] [Related]

  • 11. [Chromatographic investigation of free amino acids of the heart, kidneys and brain in experimental myocarditis].
    Andreeva LA.
    Biull Eksp Biol Med; 1966 Nov 28; 31(11):52-3. PubMed ID: 6005449
    [No Abstract] [Full Text] [Related]

  • 12. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies].
    Segni G.
    Minerva Nipiol; 1970 Nov 28; 20(4):83-110. PubMed ID: 4396023
    [No Abstract] [Full Text] [Related]

  • 13. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Nov 28; 1(1):1-11. PubMed ID: 4942066
    [No Abstract] [Full Text] [Related]

  • 14. Application of a thin-layer chromatography microtechnique for the screening of aminoacidurias in 3,165 Chinese newborns.
    Wang TR.
    Taiwan Yi Xue Hui Za Zhi; 1984 Sep 28; 83(9):869-78. PubMed ID: 6596395
    [No Abstract] [Full Text] [Related]

  • 15. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia].
    Dhondt JL, Cartigny B, Farriaux JP.
    Ann Biol Clin (Paris); 1974 Sep 28; 32(6):499-506. PubMed ID: 4468743
    [No Abstract] [Full Text] [Related]

  • 16. Genetic screening.
    Levy HL.
    Adv Hum Genet; 1973 Sep 28; 4():1-104. PubMed ID: 4593296
    [No Abstract] [Full Text] [Related]

  • 17. Simplified thin layer chromatography screening test for detection of important hyperaminoacidemias.
    Kraffczyk F, Helger R, Lang H.
    Clin Chim Acta; 1971 Feb 28; 31(2):489-91. PubMed ID: 5573693
    [No Abstract] [Full Text] [Related]

  • 18. Ion-exchange thin-layer chromatographic screening test for phenylketonuria and other aminoacidaemias.
    Kovács J.
    Acta Paediatr Acad Sci Hung; 1973 Feb 28; 14(3):165-9. PubMed ID: 4785695
    [No Abstract] [Full Text] [Related]

  • 19. [Lethal familial neonatal ketotic hyperammonemia].
    Pauli A, Huguet J, Rollet M, Cousin J, Farriaux JP, Fournier A, Navarro J, Cathelineau L, Aymard P, Saudubray JM, Polonovski C, Laplane R.
    Arch Fr Pediatr; 1972 Feb 28; 29(7):699-712. PubMed ID: 4644460
    [No Abstract] [Full Text] [Related]

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

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