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Journal Abstract Search

400 related items for PubMed ID: 5267129

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

  • 2. [A screening test for phenylketonuria using a paper chromatography method].
    Halvorsen S, Skjelkvåle L.
    Lakartidningen; 1974 Mar 20; 71(12):1166-7. PubMed ID: 4821497
    [No Abstract] [Full Text] [Related]

  • 3. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia].
    Dhondt JL, Cartigny B, Farriaux JP.
    Ann Biol Clin (Paris); 1974 Mar 20; 32(6):499-506. PubMed ID: 4468743
    [No Abstract] [Full Text] [Related]

  • 4. Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood.
    Partington MW.
    Can Med Assoc J; 1968 Oct 05; 99(13):638-44. PubMed ID: 5685509
    [No Abstract] [Full Text] [Related]

  • 5. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL.
    Clin Endocrinol Metab; 1974 Mar 05; 3(1):153-66. PubMed ID: 4609646
    [No Abstract] [Full Text] [Related]

  • 6. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism].
    Charpentier C, Lemonnier A.
    Ann Biol Clin (Paris); 1969 Mar 05; 27(5):297-323. PubMed ID: 4897889
    [No Abstract] [Full Text] [Related]

  • 7. Neonatal hyperphenylalaninemia: a differential diagnosis.
    Menkes JH, Holtzman NA.
    Neuropadiatrie; 1970 Apr 05; 1(4):434-46. PubMed ID: 5538081
    [No Abstract] [Full Text] [Related]

  • 8. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].
    Boisse J.
    Presse Med (1893); 1968 Apr 20; 76(19):903-6. PubMed ID: 5645352
    [No Abstract] [Full Text] [Related]

  • 9. [Hyperphenylalaninemia in the neonatal period].
    Spahr A.
    Rev Med Suisse Romande; 1973 Sep 20; 93(9):679-86. PubMed ID: 4769047
    [No Abstract] [Full Text] [Related]

  • 10. [Comparison of free amino acids in capillary and venous blood serum of children and adolescents with phenylketonuria and leucinosis].
    Liappis N, Schlebusch H, Mallmann R.
    Klin Padiatr; 1992 Sep 20; 204(2):107-10. PubMed ID: 1583848
    [Abstract] [Full Text] [Related]

  • 11. [Hyperphenylalaninemia and other hyperaminoacidurias with mental retardation, detected by multiple screening].
    Hyánek J.
    Cas Lek Cesk; 1972 Sep 20; 111(8):176-8. PubMed ID: 5010326
    [No Abstract] [Full Text] [Related]

  • 12. 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 Sep 20; 27(5):334-47. PubMed ID: 4779694
    [No Abstract] [Full Text] [Related]

  • 13. The place of large-scale screening in the prevention of hereditary diseases. Phenylketonuria.
    Szeinberg A, Cohen BE.
    Isr J Med Sci; 1973 Sep 20; 9(9):1319-22. PubMed ID: 4775112
    [No Abstract] [Full Text] [Related]

  • 14. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Sep 20; 1(1):1-11. PubMed ID: 4942066
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. [Examination technics in metabolic brain damage with special reference to thin-layer chromatography].
    Lothaller H, Rett A, Zimprich H.
    Wien Klin Wochenschr; 1971 Nov 26; 83(47):863-6. PubMed ID: 4257065
    [No Abstract] [Full Text] [Related]

  • 17. [Screening for aminoacidopathies in newborns by means of an aminoacid analyzer. Reference values and statistical determinations (author's transl)].
    Antonozzi I, Del Castello PG, Morisi G, Ceccarelli P.
    Ann Ist Super Sanita; 1978 Nov 26; 14(4):781-91. PubMed ID: 756692
    [Abstract] [Full Text] [Related]

  • 18. [Mass screening of phenylketonuria. Report on a screening center (October 1967-December 1968)].
    Barbesier J, Boisse J, Charpentier C, Lemonnier A, Mozziconacci P.
    Presse Med (1893); 1969 Sep 13; 77(37):1279-82. PubMed ID: 4897489
    [No Abstract] [Full Text] [Related]

  • 19. [Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1].
    Menne F, Enzenauer J, Matz D.
    Med Klin; 1976 Apr 23; 71(17):724-8. PubMed ID: 775276
    [No Abstract] [Full Text] [Related]

  • 20. [Disorders of amino acid metabolism (author's transl)].
    Hirano S.
    Tanpakushitsu Kakusan Koso; 1977 Apr 23; 22(6):776-83. PubMed ID: 337387
    [No Abstract] [Full Text] [Related]

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