Genetic hemochromatosis in Italian patients with prophyria cutanea tarda: possible explanation for iron overload-Reference-Cited by-同舟云学术

Genetic hemochromatosis in Italian patients with prophyria cutanea tarda: possible explanation for iron overload

Published:1996-05 Issue:5 Volume:24 Page:564-569
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Fargion Silvia,Ludovica Fracanzani Anna,Romano Riccardo,Cappellini Maria Domenica,Faré Maristella,Mattioli Michela,Piperno Alberto,Ronchi Guido,Fiorelli Gemino

Publisher

Elsevier BV

Subject

Hepatology

Reference43 articles.

1. Hepatic siderosis and porphyria cutanea tarda: relation of iron excess to the metabolic defect;Felsher;Semin Hematol,1977

2. Iron storage in porphyria cutanea tarda;Lundvall;Acta Med Scand,1970

3. Red-cell uroporphyrinogen decarboxylase activity in porphyria cutanea tarda;Felsher;N Engl J MEd,1982

4. Familial and sporadic porphyria cutanea tarda: two different diseases;De Verneuil;Hum Genet,1978

5. Disorders of porphyrin metabolism;Cohen,1990

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2. Hemochromatosis and Iron Storage Disorders;Schiff's Diseases of the Liver;2017-10-23

3. Precipitating factors of porphyria cutanea tarda in Brazil with emphasis on hemochromatosis gene (HFE) mutations. Study of 60 patients;Anais Brasileiros de Dermatologia;2013-08

4. Review article: the iron overload syndromes;Alimentary Pharmacology & Therapeutics;2012-03-04

5. Disorders associated with systemic or local iron overload: from pathophysiology to clinical practice;Metallomics;2011