Genetic hemochromatosis in Italian patients with prophyria cutanea tarda: possible explanation for iron overload (Q62607299)

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18 October 2019

title

Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overload (English)

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18 October 2019

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2

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Maria Domenica Cappellini

18 October 2019

4

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18 October 2019

Michela Mattioli

6

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18 October 2019

Alberto Piperno

7

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18 October 2019

author name string

S Fargion

1

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18 October 2019

R Romano

3

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18 October 2019

M Faré

5

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18 October 2019

G Ronchi

8

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18 October 2019

G Fiorelli

9

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18 October 2019

publication date

1 May 1996

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18 October 2019

published in

Journal of Hepatology

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18 October 2019

volume

24

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18 October 2019

issue

5

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18 October 2019

page(s)

564-569

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Iron storage in porphyria cutanea tarda

18 October 2019

cites work

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7 January 2021

Decreased hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda

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7 January 2021

Familial and sporadic porphyria cutanea: two different diseases

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7 January 2021

Immunoreactive uroporphyrinogen decarboxylase in the liver in porphyria cutanea tarda

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7 January 2021

Enzyme heterogeneity in the porphyrias

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7 January 2021

Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association

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7 January 2021

The effect of phlebotomy therapy in porphyria cutanea tarda. Its relation to the phlebotomy-induced reduction of iron stores

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7 January 2021

Heterozygosity for HLA-linked hemochromatosis as a likely cause of the hepatic siderosis associated with sporadic porphyria cutanea tarda

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7 January 2021

Porphyria cutanea tarda and HLA-linked hemochromatosis

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7 January 2021

Porphyria cutanea tarda and HLA-linked hemochromatosis. Evidence against a systematic association

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7 January 2021

Increased frequency of HLA-A3 in subjects with sporadic porphyria cutanea tarda

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7 January 2021

Porphyria cutanea tarda and HLA-linked hemochromatosis--all in the family?

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7 January 2021

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

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7 January 2021

Prevalence of hereditary haemochromatosis in two Swedish urban areas

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Prevalence of haemochromatosis amongst asymptomatic Australians

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7 January 2021

Immunohistochemical evidence for a lack of ferritin in duodenal absorptive epithelial cells in idiopathic hemochromatosis.

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7 January 2021

Gluconate metabolism of Pasteurellapestis

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7 January 2021

Measurement of liver-iron concentration in needle-biopsy specimens

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7 January 2021

Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda

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7 January 2021

The Measurement of Total and Unsaturated Iron-Binding Capacity in Serum

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7 January 2021

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7 January 2021

Porphyria cutanea tarda and haemochromatosis: a family study

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7 January 2021

Liver pathology in genetic hemochromatosis: a review of 135 homozygous cases and their bioclinical correlations

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7 January 2021

HLA typing in 67 Italian patients with idiopathic hemochromatosis and their relatives

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7 January 2021

Iron metabolism in porphyria cutanea tarda

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7 January 2021

Regulation of transferrin, transferrin receptor, and ferritin genes in human duodenum

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7 January 2021

Serum Ferritin in Alcoholics and the Relation to Liver Damage, Iron State and Erythropoietic Activity

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Liver damage in Italian patients with hereditary hemochromatosis is highly influenced by hepatitis B and C virus infection

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7 January 2021

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7 January 2021

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Identifiers

DOI

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18 October 2019

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