The occurrence of hepatoma in the chronic form of hereditary tyrosinemia

Author:

Weinberg Arthur G.,Mize Charles E.,Worthen Howard G.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference61 articles.

1. Tyrosinémié héréditaire. I. Etude clinique et biologique de 62 cas;Larochelle;Pediatrie,1973

2. Studies on tyrosinosis: activity of the transaminase, parahydroxyphenylpyruvate oxidase and homogenetisic acid oxidase;Taniguchi;Br Med J,1965

3. The enzymatic deficiency in tyrosinemia;La Du;Am J Dis Child,1967

4. Tyrosinemia. An inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal tubular defects (de Toni-Debre-Fanconi syndrome);Gentz;J Pediatr,1965

5. An atypical case of tyrosinosis. III. The outcome of the patient: pathological and biochemical observations on the organ tissues;Sakai;Jikeikai Med J,1959

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