Literature DB >> 6133038

A new variant form of hypertyrosinaemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency.

F Endo, A Kitano, I Uehara, N Nagata, I Matsuda, T Shinka, T Kuhara, I Matsumoto.   

Abstract

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Year:  1982        PMID： 6133038     DOI： 10.1007/bf02179153

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  The enzymatic conversion of homogentisic acid to 4-fumarylacetoacetic acid.

Authors:  R G RAVDIN; D I CRANDALL
Journal:  J Biol Chem       Date:  1951-03       Impact factor: 5.157

2.  Radiochemical assays for p-hydroxyphenylpyruvate hydroxylase activity in human liver.

Authors:  B Lindblad
Journal:  Clin Chim Acta       Date:  1971-08       Impact factor: 3.786

3.  Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia.

Authors:  R Berger; G P Smit; S A Stoker-de Vries; M Duran; D Ketting; S K Wadman
Journal:  Clin Chim Acta       Date:  1981-07-18       Impact factor: 3.786

4.  On the enzymic defects in hereditary tyrosinemia.

Authors:  B Lindblad; S Lindstedt; G Steen
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205
  4 in total

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