Evidence That Hepatic Crystalline Deposits in a Patient with Protoporphyria Are Composed of Protoporphyrin

Author:

Bloomer Joseph R.,Enriquez Rosa

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference21 articles.

1. Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts;Bonkowsky;J Clin Invest,1975

2. Diminished erythroid ferrochelatase activity in protoporphyria;Bottomley;J Lab Clin Med,1975

3. Decreased haem synthetase activity in blood cells of patients with erythropoietic protoporphyria;deGeoij;Eur J Clin Invest,1975

4. Inheritance in protoporphyria: Comparison of heme synthetase activity in skin fibroblasts with clinical features;Bloomer;Lancet,1976

5. Pathogenesis and therapy of liver disease in protoporphyria;Bloomer;Yale J Biol Med,1979

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1. Erythropoietic protoporphyrias: Pathogenesis, diagnosis and management;Liver International;2024-07-16

2. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024

3. Porphyrias: Acute Manifestations;Contemporary Endocrinology;2021

4. Heme biosynthesis and the porphyrias;Molecular Genetics and Metabolism;2019-11

5. Developmental and Inherited Liver Disease;Macsween's Pathology of the Liver;2018

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