Literature DB >> 3977399

Coagulation defect of congenital tyrosinaemia.

S Ozsoylu.   

Abstract

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Year:  1985        PMID： 3977399      PMCID： PMC1777131          DOI： 10.1136/adc.60.2.188-b

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  5 in total

1.  Galactokinase deficiency: clinical and biochemical findings in a new kindred.

Authors:  W R Pickering; R R Howell
Journal:  J Pediatr       Date:  1972-07       Impact factor: 4.406

2.  Coagulation defect of congenital tyrosinaemia.

Authors:  D I Evans; I B Sardharwalla
Journal:  Arch Dis Child       Date:  1984-11       Impact factor: 3.791

3.  Acquired dysfibrinogenaemia in acute and chronic liver disease.

Authors:  D A Lane; M F Scully; D P Thomas; V V Kakkar; I L Woolf; R Williams
Journal:  Br J Haematol       Date:  1977-02       Impact factor: 6.998

4.  Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemia.

Authors:  M K Hostetter; H L Levy; H S Winter; G J Knight; J E Haddow
Journal:  N Engl J Med       Date:  1983-05-26       Impact factor: 91.245

5.  Tyrosine metabolism in cirrhosis.

Authors:  B M Nordlinger; J T Fulenwider; G L Ivey; B A Faraj; F M Ali; M Kutner; J M Henderson; D Rudman
Journal:  J Lab Clin Med       Date:  1979-12
  5 in total

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