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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

181 related items for PubMed ID: 4257065

  • 41.
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  • 47. [Laboratory examinations for inborn errors of metabolism].
    Kawamura M.
    Rinsho Byori; 1986 Feb; 34(2):133-5. PubMed ID: 3702083
    [No Abstract] [Full Text] [Related]

  • 48. Rapid automated quantitation of isoleucine, leucine, tyrosine and phenylalanine from dried blood filter paper specimens.
    Qu Y, Miller JB, Slocum RH, Shapira E.
    Clin Chim Acta; 1991 Dec 16; 203(2-3):191-7. PubMed ID: 1777980
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  • 50. Screening for inherited metabolic diseases using gas chromatography-tandem mass spectrometry (GC-MS/MS) in Sichuan, China.
    Wang H, Wang X, Li Y, Dai W, Jiang D, Zhang X, Cui Y.
    Biomed Chromatogr; 2017 Apr 16; 31(4):. PubMed ID: 27598852
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  • 52. Neonatal screening for congenital disorders.
    Gudat JC, Maclaren NK.
    J Fla Med Assoc; 1980 Feb 16; 67(2):137-42. PubMed ID: 7359105
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  • 53. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities.
    Wadman SK.
    Acta Univ Carol Med Monogr; 1977 Feb 16; (77 Pt 1):49-69. PubMed ID: 615451
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  • 56. [Screening for congenital metabolic disorders. Indication and results].
    Bickel H.
    Monatsschr Kinderheilkd; 1983 Jun 16; 131(6):323-7. PubMed ID: 6888386
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  • 57. Plasma amino acid pattern at noon in early treated hyperphenylalaninemic, phenylketonuric, and normal children.
    Held KR, Koepp P, Plettner C, Grüttner R.
    Ann Nutr Metab; 1983 Jun 16; 27(4):278-85. PubMed ID: 6881914
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