Familial and sporadic porphyria cutanea: two different diseases

Author:

De Verneuil H.,Nordmann Y.,Phung N.,Grandchamp B.,Aitken G.,Grelier M.,Noire J.

Publisher

Elsevier BV

Subject

Biochemistry

Reference14 articles.

1. Porphyria cutanea tarda in South Africa: the metabolic basis of disordered haem biosynthesis;Blekkenhorst,1976

2. The simultaneous separation and washing of erythrocytes;Blincoe;Clin. Chim. Acta,1974

3. Studies of the uroporphyrins III. An improved method for the decarboxylation of uroporphyrin;Edmondson;J. blol. Chem.,1953

4. Identification of a group of tetracar-boxylate porphyrins. containing one acetate and three propionate β-substituents, in faeces from patients with symptomatic cutaneous hepatic porphyria and from rats with porphyria due to hexachlorobenzene;Elder;Biochem. J.,1972

5. Porphyrin metabolism in porphyria cutanea tarda;Elder;Sem. Hemat.,1975

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1. Les porphyries héréditaires : anomalies du métabolisme de l’hème;Bulletin de l'Académie Nationale de Médecine;2014-06

2. Porphyrias;The Lancet;2010-03

3. Complex Gene−Chemical Interactions: Hepatic Uroporphyria As a Paradigm;Chemical Research in Toxicology;2010-01-25

4. Chapter 6 Disruption of Heme Synthesis by Polyhalogenated Aromatics;Advances in Molecular Toxicology;2009

5. Chronische hepatische Porphyrie mit Uroporphyrinogen-Decarboxylase-Defekt in vier Generationen;DMW - Deutsche Medizinische Wochenschrift;2008-03-26

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