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PUBMED FOR HANDHELDS

Journal Abstract Search

92 related items for PubMed ID: 5070934

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  • 4. [Hypermethioninemia in the differential diagnosis of infantile obstructive jaundice (author's transl)].
    Schmid-Rüter E, Feist D.
    Monatsschr Kinderheilkd (1902); 1976 Nov; 124(11):744-7. PubMed ID: 995134
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  • 5. A patient with tyrosinemia and hypermethioninemia.
    Partington MW, Haust MD.
    Can Med Assoc J; 1967 Oct 28; 97(18):1059-67. PubMed ID: 6050907
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  • 6. Spectrum of hypermethioninemia in neonatal screening.
    Chien YH, Chiang SC, Huang A, Hwu WL.
    Early Hum Dev; 2005 Jun 28; 81(6):529-33. PubMed ID: 15935930
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  • 7. [Hypertyrosinemia with hypermethioninemia in the newborn in a case of fructose intolerance].
    Willems C, Heusden A, Renson P, Legat C, Monard Y, Stainier L.
    Helv Paediatr Acta; 1971 Oct 28; 26(4):467-81. PubMed ID: 5123311
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  • 11. [Fructose intolerance associated with hypermethioninemia in a young infant].
    Korányi G, Bartók I, Vészi Z.
    Orv Hetil; 1980 Aug 31; 121(35):2137-40. PubMed ID: 7465175
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  • 13. Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia.
    Gaull GE, Tallan HH.
    Science; 1974 Oct 04; 186(4158):59-60. PubMed ID: 4421454
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  • 14. [Biliary atresia: pathogenetic considerations emerging from the histopathologic analysis of the liver parenchyma].
    Farolfi A, Cattaneo M, Varenna R, Portaleone D, Ferrentino R, Carnelli V.
    Pediatr Med Chir; 1983 Oct 04; 5(3):69-73. PubMed ID: 6647066
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  • 18. Partial proximal 10q trisomy: a new case associated with biliary atresia.
    Lysy PA, Sibille C, Gillerot Y, Smets F, Sokal EM.
    Hereditas; 2007 Nov 04; 144(5):191-4. PubMed ID: 18031353
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  • 19. [Trisomy 18. Case report].
    Zanetti P, De Sanctis C.
    Minerva Pediatr; 1969 Oct 13; 21(41):1910-5. PubMed ID: 5391364
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