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Journal Abstract Search

98 related items for PubMed ID: 732094

  • 1. [Frequency of transitorial tyrosinemia of the newborn infant].
    Basys V, Machill G.
    Kinderarztl Prax; 1978 Nov; 46(11):575-80. PubMed ID: 732094
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  • 3. [A system of early screening for inborn errors of metabolism: methods and results for hereditary tyrosinemia].
    Bélanger M, Saint-Hilaire B, Bélanger L.
    Union Med Can; 1973 Feb; 102(2):294-302. PubMed ID: 4709460
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  • 5. Keratopathy in tyrosinemia.
    Burns RP, Gipson IK, Murray MJ.
    Birth Defects Orig Artic Ser; 1976 Feb; 12(3):169-80. PubMed ID: 8172
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  • 7. [Hereditary tyrosinemia and alpha-1-fetoprotein. I. Clinical value of alpha-fetoprotein in hereditary tyrosinemia].
    Bélanger L, Bélanger M, Prive L, Larochelle J, Tremblay M, Aubin G.
    Pathol Biol (Paris); 1973 May; 21(5):449-55. PubMed ID: 4125220
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  • 13. [A rare cause of neonatal hyperphenylalaninemia: tyrosinemia type I].
    Sarles J, Maurin N, Giraud F.
    Pediatrie; 1992 May; 47(12):809-11. PubMed ID: 1338924
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  • 15. The enzymatic deficiency in tyrosinemia.
    Du BN.
    Can Med Assoc J; 1967 Oct 28; 97(18):1076-8. PubMed ID: 6050909
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  • 17. [Hereditary tyrosinemia in an acute form: a case report (author's transl)].
    Di Battista C, Rossi L, Marcelli P, Di Saverio P, Laudizi Z, Moretti P.
    Pediatr Med Chir; 1981 Oct 28; 3(1):101-4. PubMed ID: 6975468
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