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Journal Abstract Search

159 related items for PubMed ID: 7987467

  • 1. [Protocol of metabolic investigations in hereditary metabolic diseases].
    Poggi F, Rabier D, Vassault A, Charpentier C, Kamoun P, Saudubray JM.
    Arch Pediatr; 1994 Jul; 1(7):667-73. PubMed ID: 7987467
    [Abstract] [Full Text] [Related]

  • 2. Perimortem laboratory investigation of genetic metabolic disorders.
    Christodoulou J, Wilcken B.
    Semin Neonatol; 2004 Aug; 9(4):275-80. PubMed ID: 15251144
    [Abstract] [Full Text] [Related]

  • 3. An approach to the diagnosis of metabolic diseases.
    Barness LA.
    Fetal Pediatr Pathol; 2004 Jan; 23(1):3-10. PubMed ID: 15371119
    [Abstract] [Full Text] [Related]

  • 4. [Biochemical diagnosis of rare hereditary metabolic disorders. Experiences from a patient sample of the Innsbruck University Pediatric Clinic 1984-1987].
    Sperl W.
    Padiatr Padol; 1990 Jan; 25(3):157-67. PubMed ID: 2381732
    [Abstract] [Full Text] [Related]

  • 5. [Congenital metabolic diseases as a cause of acute illnesses in the neonatal period].
    Stöckler S, Ipsiroglu OS, Paschke E.
    Klin Padiatr; 1989 Jan; 201(5):369-72. PubMed ID: 2677512
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  • 7. [A staged plan for laboratory diagnosis of hereditary metabolic diseases].
    Zöllner H, Tittelbach-Helmrich W, Bannert N, Cario WR, Pelz L, Seidlitz G, Cobet G, Wiedemann G, Zinsmeyer J, Beier L.
    Kinderarztl Prax; 1989 Dec; 57(12):623-6. PubMed ID: 2625844
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  • 9. Clinical and laboratory approach to a neonate suspected of an inborn error of metabolism.
    Kang ES.
    Turk J Pediatr; 1999 Dec; 41(1):1-35. PubMed ID: 10770673
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  • 11. Human biochemical genetics: an insight into inborn errors of metabolism.
    Yu C, Scott CR.
    J Zhejiang Univ Sci B; 2006 Feb; 7(2):165-6. PubMed ID: 16421978
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  • 14. Information system for the support of research, diagnosis and therapy of inborn metabolic diseases.
    Kauert R, Töpel T, Scholz U, Hofestädt R.
    Stud Health Technol Inform; 2001 Feb; 84(Pt 1):353-6. PubMed ID: 11604762
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  • 15. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D, Tebib N, Kaabachi N, Ben Dridi MF, Mebazaa A.
    Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277
    [No Abstract] [Full Text] [Related]

  • 16. [Screening of newborns for inborn errors of metabolism by tandem mass spectrometry].
    Simonsen H.
    Ugeskr Laeger; 2002 Nov 25; 164(48):5607-12. PubMed ID: 12523003
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  • 17. [Clinical approach to hereditary metabolic disorders in neonates. Review of 20 years' experience].
    Saudubray JM, Ogier H, Bonnefont JP, Munich A, Lombes A, Hervé F, Mitchel G, Poll The B, Specola N, Parvy B.
    Cesk Pediatr; 1990 Jan 25; 45(1):1-6. PubMed ID: 2393916
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  • 18. [Metabolic errors in newborn infants--diagnosis and treatment].
    Handeland M.
    Tidsskr Nor Laegeforen; 2001 Mar 10; 121(7):822-6. PubMed ID: 11301707
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  • 19. [Multiple screening tests for hereditary metabolic diseases. Clinical problems and questions of interpretation].
    Lanza I.
    Minerva Pediatr; 1975 Nov 24; 27(37):2054-64. PubMed ID: 1232538
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