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PUBMED FOR HANDHELDS

Journal Abstract Search

141 related items for PubMed ID: 5154330

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  • 3. Amino acid screening of mentally defective patients by high voltage electrophoresis.
    Meyer JS, Wood MJ.
    Mo Med; 1972 Feb; 69(2):112-6. PubMed ID: 5058792
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  • 5. High-voltage electrophoresis in urinary amino acid screening.
    Holmgren G, Jeppson JO, Samuelson G.
    Scand J Clin Lab Invest; 1970 Dec; 26(4):313-8. PubMed ID: 5486398
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  • 6. [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; 102(2):294-302. PubMed ID: 4709460
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  • 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 Feb; 27(5):334-47. PubMed ID: 4779694
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  • 9. [Study of aminoaciduria and aminoacidemia by chromato-ion-ophoresis. Technic and application to the dynamic study of various amino acid metabolic disorders].
    Vovan L, Perrimond H, Pierron H, Orsini A.
    Pediatrie; 1967 Sep; 22(6):732-3. PubMed ID: 5621096
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  • 10. Aminoacidopathies in mental retardation.
    Brante G, Börjesson M, Rayner S.
    Monogr Hum Genet; 1972 Sep; 6():146-7. PubMed ID: 4663889
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  • 13. Urinary metabolic screening in children with psycho-neurological diseases. Evaluation of different screening tests.
    Hambraeus L, Holmgren G.
    Ups J Med Sci Suppl; 1974 Sep; 15():1-23. PubMed ID: 4274307
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  • 15. [Hyperphenylalaninemia and other hyperaminoacidurias with mental retardation, detected by multiple screening].
    Hyánek J.
    Cas Lek Cesk; 1972 Sep; 111(8):176-8. PubMed ID: 5010326
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  • 18. [Studies of inborn errors of amino acid metabolism and urinary excretion of -phenylethylamine, using screening methods].
    Berio A.
    Minerva Pediatr; 1972 Jun 23; 24(32):937-41. PubMed ID: 5050421
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  • 19. Screening for amino acid disorders using prepared thin layers of cellulose on aluminium foil.
    Ersser RS.
    J Med Lab Technol; 1970 Apr 23; 27(2):142-53. PubMed ID: 5450263
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  • 20. [Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)].
    Lubs H, Baumann H, Kluge G, Machill G.
    Laryngol Rhinol Otol (Stuttg); 1974 Sep 23; 53(9):648-51. PubMed ID: 4419508
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