Tyrosin�mie Typ I

Author:

Rodeck B.,Baumann U.

Publisher

Springer Science and Business Media LLC

Subject

Surgery,Pediatrics, Perinatology, and Child Health

Reference29 articles.

1. Lindblad B, Lindstedt S, Steen G (1977) On the enzymic defects in hereditary tyrosinemia. Proc Natl Acad Sci USA 74:4641?4645

2. Mitchell GA, Lambert M, Tanguay RM (1995) Hypertyrosinemia. In: Scriver CR, Beaudet AL, Sly WS et al. (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 1077?1106

3. Lindblad A, Lindstedt G, Lindstedt S et al. (1972) Metabolism of p-hydroxyphenylpyruvate in hereditary tyrosinaemia. In: Stern J (ed) Organic acidurias. Churchill Livingstone, Edinburgh, p 63

4. Sassa S, Kappas A (1983) Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone. J Clin Invest 71:625?634

5. Sima AA, Kennedy JC, Blakeslee D et al. (1981) Experimental porphyric neuropathy: a preliminary report. Can J Neurol Sci 8:105?113

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