The Porphyrias

Author:

Prieto J.,Camps J.

Publisher

Springer Berlin Heidelberg

Reference85 articles.

1. Lim HW, Pérez HD, Goldstein IM et al. (1981) Complement-derived chemotactic activity is generated in human serum containing uroporphyrin after irradiation with 450 nm light. J Clin Invest 67:1072–1077

2. Kappas A, Sassa S, Galbraith RA et al. (1989) The porphyrias. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic basis of inherited disease. McGraw-Hill, New York, pp 1305–1365

3. Deybach JC, de Verneuil H, Boulechfar S et al. (1990) Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Gunther’s disease). Blood 75:1763–1765

4. Thunell S, Holmberg L, Lundgren J (1987) Aminolevulinate dehydratase porphyria in infancy. A clinical and biochemical study. J Clin Chem Clin Biochem 25:5–10

5. Lannfelt L, Wetterberg L, Gellerfors P et al. (1989) Mutations in acute intermittent porphyria detected by ELISA measurement of porphobilinogen deaminase. J Clin Chem Clin Biochem 27:857–862

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