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Journal Abstract Search

104 related items for PubMed ID: 483445

  • 21. [Hereditary tyrosinemia type I].
    Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):130-3. PubMed ID: 9590006
    [No Abstract] [Full Text] [Related]

  • 22. [Tyrosinemia and Richner-Hanhart syndrome (an autosomal recessive hereditary metabolic disease of childhood with bilateral dendritic pseudokeratitis, keratosis palmaris et plantaris and mental deficiency)].
    Jaeger W, Gallasch G, Schnyder UW, Lutz P, Schmidt H.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1978; (75):649-54. PubMed ID: 154319
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  • 25. Rapid nonradioactive assay for the detection of the common French Canadian tyrosinemia type I mutation.
    Grompe M, al-Dhalimy M.
    Hum Mutat; 1995; 5(1):105. PubMed ID: 7728147
    [No Abstract] [Full Text] [Related]

  • 26. Liver disease in hereditary tyrosinemia.
    Gagné R.
    N Engl J Med; 1983 Oct 27; 309(17):1063. PubMed ID: 6621647
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  • 29. Effect of dietary treatment on the renal tubular function in a patient with hereditary tyrosinemia.
    Suzuki Y, Konda M, Imai I, Imamura H, Shimao S, Okaka T.
    Int J Pediatr Nephrol; 1987 Oct 27; 8(3):171-6. PubMed ID: 3429140
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  • 32. Hereditary tyrosinemia.
    JAMA; 1968 Mar 18; 203(12):1062. PubMed ID: 5694370
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  • 35. Prenatal diagnosis of hereditary tyrosinemia.
    Steinmann B, Gitzelmann R, Kvittingen EA, Stokke O.
    N Engl J Med; 1984 Mar 29; 310(13):855-6. PubMed ID: 6700679
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  • 38. A syndrome of hereditary tyrosinemia in mink (Mustela vison Schreb.).
    Christensen K, Fischer P, Knudsen KE, Larsen S, Sørensen H, Venge O.
    Can J Comp Med; 1979 Jul 29; 43(3):333-40. PubMed ID: 487250
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  • 40. [Existence of alpha-1-fetoprotein in 8 patients with hereditary tyrosinemia. Preliminary report].
    Bélanger L, Bélanger M, Larochelle J.
    Union Med Can; 1972 May 29; 101(5):877-8. PubMed ID: 4666892
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