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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

179 related items for PubMed ID: 3074716

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  • 24. [Macular degeneration in hereditary metabolic diseases in children (inborn errors of metabolism)].
    Stanescu-Segal B, Evrard P.
    Bull Soc Belge Ophtalmol; ; 212():109-15. PubMed ID: 6545872
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  • 27. Diagnostic test for congenital hyperuricemia with central nervous system dysfunction.
    Berman PH, Balis ME, Dancis J.
    J Lab Clin Med; 1968 Feb; 71(2):247-53. PubMed ID: 5638128
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  • 30. [A cerebral atrophic syndrome in hypoammoniemia].
    Rett A.
    Monatsschr Kinderheilkd (1902); 1968 Jun; 116(6):310-1. PubMed ID: 5305197
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  • 32. [Diagnosis of encephalopathy of genetic origin (excluding chromosome abnormalities)].
    Robert JM.
    Rev Neuropsychiatr Infant; 1967 Jun; 15(4):275-86. PubMed ID: 5602321
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  • 34. Hereditary tyrosinaemia.
    Lancet; 1990 Jun 23; 335(8704):1500-1. PubMed ID: 1972437
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  • 37. Cardiac manifestations of inborn errors of metabolism.
    Evangeliou A, Papadopoulou-Legbelou K, Daphnis E, Ganotakis E, Vavouranakis I, Michailidou H, Hitoglou-Makedou A, Nicolaidou P, Wevers R, Varlamis G.
    Minerva Pediatr; 2007 Jun 23; 59(3):215-8. PubMed ID: 17519866
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