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Journal Abstract Search

156 related items for PubMed ID: 898402

  • 1. [Hereditary tyrosinemia: examination of the liver by electron microscopy of hepatic biopsies: observation of 7 cases].
    Tremblay M, Bélanger L, Larochelle J, Privé L, Gagnon PM.
    Union Med Can; 1977 Jul; 106(7):1014-6. PubMed ID: 898402
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  • 4. Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia.
    Endo F, Kitano A, Uehara I, Nagata N, Matsuda I, Shinka T, Kuhara T, Matsumoto I.
    Pediatr Res; 1983 Feb; 17(2):92-6. PubMed ID: 6828337
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  • 5. A new variant form of hypertyrosinaemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency.
    Endo F, Kitano A, Uehara I, Nagata N, Matsuda I, Shinka T, Kuhara T, Matsumoto I.
    J Inherit Metab Dis; 1982 Feb; 5(4):237-8. PubMed ID: 6133038
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  • 6. [Hereditary tyrosinemia type III].
    Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb; (18 Pt 1):137-40. PubMed ID: 9590008
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  • 7. Enzyme defect in a case of tyrosinemia type I, acute form.
    Furukawa N, Kinugasa A, Seo T, Ishii T, Ota T, Machida Y, Inoue F, Imashuku S, Kusunoki T, Takamatsu T.
    Pediatr Res; 1984 May; 18(5):463-6. PubMed ID: 6145143
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  • 9. Urinary p-tyramine in hereditary tyrosinemia: I. Levels as compared to normal individuals, effect of diet, and relationship to urinary tyrosine.
    Hoag GN, Hill A, Zaleski W.
    Clin Biochem; 1977 Feb; 10(1):24-5. PubMed ID: 837522
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  • 10. Hereditary tyrosinemia type I--an overview.
    Kvittingen EA.
    Scand J Clin Lab Invest Suppl; 1986 Feb; 184():27-34. PubMed ID: 3296130
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  • 11. Chronic tyrosinemia associated with 4-hydroxyphenylpyruvate dioxygenase deficiency with acute intermittent ataxia and without visceral and bone involvement.
    Giardini O, Cantani A, Kennaway NG, D'Eufemia P.
    Pediatr Res; 1983 Jan; 17(1):25-9. PubMed ID: 6132360
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  • 14. [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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  • 16. Urinary p-tyramine in hereditary tyrosinemia: II. Origin of urinary p-tyramine.
    Hoag GN, Hill A, Zaleski W.
    Clin Biochem; 1977 Feb; 10(1):26-8. PubMed ID: 837523
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  • 18. Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemia.
    Hostetter MK, Levy HL, Winter HS, Knight GJ, Haddow JE.
    N Engl J Med; 1983 May 26; 308(21):1265-7. PubMed ID: 6188953
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