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Literature DB >> 4785438

Iron metabolism in porphyria cutanea tarda and in erythropoietic protoporphyria.

A Turnbull, H Baker, B Vernon-Roberts, I A Magnus.

Abstract

Entities: Chemical Disease

Mesh：

Substances：
Iron Isotopes
Iron

Year: 1973 PMID： 4785438

Source DB: PubMed Journal: Q J Med ISSN： 0033-5622

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Cited

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9 in total

Review 1. The role of transferrin in the mechanism of cellular iron uptake.

Authors: K Thorstensen; I Romslo
Journal: Biochem J Date: 1990-10-01 Impact factor: 3.857

2. Professor Barrie Vernon-Roberts, AO, MD, BSc, PhD, FRCPath, FRCPA, FAOrthA (Hon), FRS.SA.

Authors: K D Rainsford; D R Haynes
Journal: Inflammopharmacology Date: 2013-07-04 Impact factor: 4.473

3. Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity.

Authors: Jasmin Barman-Aksoezen; Domenico Girelli; Caterina Aurizi; Xiaoye Schneider-Yin; Natascia Campostrini; Luca Barbieri; Elisabeth I Minder; Gianfranco Biolcati
Journal: J Inherit Metab Dis Date: 2017-02-09 Impact factor: 4.982

Review 4. Iron and the liver.

Authors: M Barry
Journal: Gut Date: 1974-04 Impact factor: 23.059

5. Microcytic anemia, erythropoietic protoporphyria, and neurodegeneration in mice with targeted deletion of iron-regulatory protein 2.

Authors: Sharon S Cooperman; Esther G Meyron-Holtz; Hayden Olivierre-Wilson; Manik C Ghosh; Joseph P McConnell; Tracey A Rouault
Journal: Blood Date: 2005-04-14 Impact factor: 22.113

Iron metabolism in porphyria cutanea tarda and in erythropoietic protoporphyria.

Review 1. The role of transferrin in the mechanism of cellular iron uptake.

2. Professor Barrie Vernon-Roberts, AO, MD, BSc, PhD, FRCPath, FRCPA, FAOrthA (Hon), FRS.SA.

3. Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity.

Review 4. Iron and the liver.

5. Microcytic anemia, erythropoietic protoporphyria, and neurodegeneration in mice with targeted deletion of iron-regulatory protein 2.

6. The role of iron in the pathogenesis of porphyria cutanea tarda. II. Inhibition of uroporphyrinogen decarboxylase.

7. An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.

8. Porphyria cutanea tarda and haemochromatosis: a family study.

Review 9. Comparison of human and bovine protoporphyria.