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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

132 related items for PubMed ID: 7883163

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  • 2. [Problems of phenotypic similarity and differential diagnostic of hereditary diseases in children].
    Barashnev IuI.
    Vestn Akad Med Nauk SSSR; 1982; (6):47-51. PubMed ID: 7051616
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  • 9. [Diagnosis and acute treatment of inborn metabolic diseases in infants].
    Lund AM, Christensen E, Skovby F.
    Ugeskr Laeger; 2002 Nov 25; 164(48):5613-9. PubMed ID: 12523004
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  • 11. Hereditary disorders including mitochondrial diseases.
    Lightowlers RN.
    Curr Opin Neurol Neurosurg; 1992 Jun 25; 5(3):368-74. PubMed ID: 1623266
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  • 12. Perimortem laboratory investigation of genetic metabolic disorders.
    Christodoulou J, Wilcken B.
    Semin Neonatol; 2004 Aug 25; 9(4):275-80. PubMed ID: 15251144
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  • 14. [Automated genetic register and computer support for the physician's diagnostic decisions].
    Kobrinskiĭ BA, Kazantseva LZ, Fel'dman AE, Babichev EM, Belitskaia TT, Belova NA, Kudriavtsev AM, Nikolaeva EA, Novikov PV, Semiachkina AN.
    Genetika; 1993 Oct 25; 29(10):1733-40. PubMed ID: 8307362
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  • 20. Assessment of the infant with acute metabolic problems.
    Wiltse HE.
    Ann Clin Lab Sci; 1991 Oct 25; 21(1):40-55. PubMed ID: 2012379
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