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PUBMED FOR HANDHELDS

Journal Abstract Search


140 related items for PubMed ID: 4933289

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Multiple neonatal screening for aminoacidopathies by ion exchange chromatography.
    Antonozzi I, Santagata G, Tofani R.
    Ric Clin Lab; 1982; 12(3):507-15. PubMed ID: 7134749
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Screening for inherited metabolic diseases.
    Komrower GM, Sardharwalla IB.
    Br Med J; 1972 Aug 19; 3(5824):476. PubMed ID: 5069242
    [No Abstract] [Full Text] [Related]

  • 25. [Screening for amino acid diseases: column chromatography of amino acids from a paper sampling].
    Castets JC, Jérome H.
    Arch Fr Pediatr; 1972 Aug 19; 29(6):675-6. PubMed ID: 5078374
    [No Abstract] [Full Text] [Related]

  • 26. [Areas of applicability of thin-layer chromatography. Practical mass screening; data on intestinal mucosa lesions].
    Szabó B.
    Padiatr Padol; 1983 Aug 19; 18(2):105-11. PubMed ID: 6856315
    [Abstract] [Full Text] [Related]

  • 27. [Diagnostic methods for the detection of amino acid metabolism disorders].
    Lutz P.
    Monatsschr Kinderheilkd (1902); 1973 May 19; 121(5):184-9. PubMed ID: 4197345
    [No Abstract] [Full Text] [Related]

  • 28. 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 19; 117(1):96-103. PubMed ID: 5812761
    [No Abstract] [Full Text] [Related]

  • 29. [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
    [No Abstract] [Full Text] [Related]

  • 30. [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]

  • 31. Selective newborn screening of inborn errors of amino acids, organic acids and fatty acids metabolism in the Kingdom of Bahrain.
    Golbahar J, Al-Jishi EA, Altayab DD, Carreon E, Bakhiet M, Alkhayyat H.
    Mol Genet Metab; 2013 Dec 31; 110(1-2):98-101. PubMed ID: 23916421
    [Abstract] [Full Text] [Related]

  • 32. Plasma amino acids during the first 24 hours of life: feasibility of early diagnosis in the newborn at risk of amino acid disorders.
    Caruso U, Cerone R, Fantasia AR, Schiaffino MC, Zignego G, Romano C.
    J Inherit Metab Dis; 1989 Dec 31; 12 Suppl 2():311-4. PubMed ID: 2512432
    [No Abstract] [Full Text] [Related]

  • 33. [Transitory neonatal disorders of amino acid metabolism].
    Lambotte C, Dodinval-Versie J, Adam A.
    Rev Med Liege; 1975 Sep 01; 30(17):579-86. PubMed ID: 1166174
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Rapid screening of aminoacidurias.
    Ganger C.
    Am J Med Technol; 1971 Nov 01; 37(11):434-9. PubMed ID: 5154330
    [No Abstract] [Full Text] [Related]

  • 36. [Early diagnosis of congenital metabolic diseases].
    Steuer W.
    Rev Clin Esp; 1971 Jun 30; 121(6):521-6. PubMed ID: 5131308
    [No Abstract] [Full Text] [Related]

  • 37. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities.
    Wadman SK.
    Acta Univ Carol Med Monogr; 1977 Jun 30; (77 Pt 1):49-69. PubMed ID: 615451
    [No Abstract] [Full Text] [Related]

  • 38. Mass screening for aminoacid disorders.
    Lancet; 1969 Jun 07; 1(7606):1133-4. PubMed ID: 4182691
    [No Abstract] [Full Text] [Related]

  • 39. Letter: Aminoacidopathies in Guam.
    Shih VE, Brink EW, Peneva P, Brody JA.
    Lancet; 1974 Apr 07; 1(7859):681. PubMed ID: 4132347
    [No Abstract] [Full Text] [Related]

  • 40. [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 07; 22(6):732-3. PubMed ID: 5621096
    [No Abstract] [Full Text] [Related]


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