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Journal Abstract Search

140 related items for PubMed ID: 4933289

  • 41. [Significance of free amino acid analysis in clinical tests].
    Hirayama C, Suyama Y, Kohno M.
    Nihon Rinsho; 1989 Dec; 48 Suppl():382-5. PubMed ID: 2621906
    [No Abstract] [Full Text] [Related]

  • 42. Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosis.
    Hyánek J, Trnka V, Homolka J, Seemanová E, Macek M, Dolezal A, Wünschová N, Hoza J, Kapras J, Kunová V, Tauchmanová H.
    Acta Univ Carol Med Monogr; 1977 Dec; (79 Pt 3):15-21. PubMed ID: 615475
    [Abstract] [Full Text] [Related]

  • 43. [Paper chromatography in the detection of aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2123-4. PubMed ID: 5136311
    [No Abstract] [Full Text] [Related]

  • 44. Screening for inborn errors of amino acid metabolism.
    Wu JT.
    Ann Clin Lab Sci; 1991 Dec 22; 21(2):123-42. PubMed ID: 2029175
    [Abstract] [Full Text] [Related]

  • 45. [Our preliminary experiences with a unidimensional paper-chromatographic technic for the study of aminoacidopathies and pathological infantile aminoacidurias].
    Scorza PA, Berni M, Cicognani A.
    Clin Pediatr (Bologna); 1967 May 22; 49(5):246-56. PubMed ID: 6083020
    [No Abstract] [Full Text] [Related]

  • 46. [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 May 22; 14(4):781-91. PubMed ID: 756692
    [Abstract] [Full Text] [Related]

  • 47. [Personal results in screening amino acid diseases by means of the method of Scriver et al].
    Di Stefano A, Berio A, Viglione M, Liotta A, Piovano B, Bellati R.
    Minerva Pediatr; 1970 Mar 10; 22(10):461-70. PubMed ID: 5444384
    [No Abstract] [Full Text] [Related]

  • 48. Detection of inborn errors of metabolism in unselected patients from pediatric intensive care units in Porto Alegre, Brazil: evaluation of screening techniques.
    Wannmacher CM, Wajner M, Buchalter MS, Dutra-Filho CS, Pellini VB, Pedroso DL, Branco FS, Goldani MZ, Bolner AR.
    Braz J Med Biol Res; 1987 Mar 10; 20(1):11-23. PubMed ID: 3690043
    [Abstract] [Full Text] [Related]

  • 49. [Mass screening of genetic metabolic abnormalities with special reference to amino acid metabolism disorders, using chemical methods].
    Lubs H, Knapp A.
    Z Arztl Fortbild (Jena); 1970 May 15; 64(10):516-9. PubMed ID: 5520559
    [No Abstract] [Full Text] [Related]

  • 50. Amino acid screening of mentally defective patients by high voltage electrophoresis.
    Meyer JS, Wood MJ.
    Mo Med; 1972 Feb 15; 69(2):112-6. PubMed ID: 5058792
    [No Abstract] [Full Text] [Related]

  • 51. Sensitive detection of amino acids in human serum and dried blood disc of 3 mm diameter for diagnosis of inborn errors of metabolism.
    Watanabe Y, Imai K.
    J Chromatogr; 1984 Aug 10; 309(2):279-86. PubMed ID: 6480779
    [Abstract] [Full Text] [Related]

  • 52. [Chromatographic analysis in the diagnosis of metabolic aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2125-8. PubMed ID: 5136312
    [No Abstract] [Full Text] [Related]

  • 53. [Screening for congenital metabolic disorders].
    Knapp A, Machill G.
    Kinderarztl Prax; 1974 Jun 22; 42(6):270-7. PubMed ID: 4610264
    [No Abstract] [Full Text] [Related]

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