The cutaneous porphyrias: a review. The British Photodermatology Group (Q33610809)

28 July 2017

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title

The cutaneous porphyrias: a review. The British Photodermatology Group (English)

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28 July 2017

Murphy GM

1

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28 July 2017

language of work or name

English

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publication date

1 April 1999

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British Journal of Dermatology

28 July 2017

published in

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28 July 2017

volume

140

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28 July 2017

issue

4

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28 July 2017

page(s)

573-581

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New type of hepatic porphyria with porphobilinogen synthase defect and intermittent acute clinical manifestation

28 July 2017

cites work

1 reference

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HCV infection in porphyria cutanea tarda

21 January 2018

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Porphyria cutanea tarda and antibodies to hepatitis C virus.

21 January 2018

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Haemophilia, hepatitis and porphyria

21 January 2018

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Porphyrin abnormalities in acquired immunodeficiency syndrome

21 January 2018

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Discoid lupus erythematosus and porphyria cutanea tarda

21 January 2018

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Porphyria cutanea tarda after allogeneic bone marrow transplantation for chronic myelogenous leukemia.

21 January 2018

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Porphyria cutanea tarda and hematologic malignancy ‐ a report of 4 cases

21 January 2018

1 reference

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A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patients

21 January 2018

1 reference

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Low-dose oral chloroquine in the treatment of porphyria cutanea tarda

21 January 2018

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Treatment of porphyria cutanea tarda of end-stage renal disease with erythropoietin

21 January 2018

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Erythropoietic protoporphyria 10 years experience

21 January 2018

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Treatment of erythropoietic protoporphyria with N-acetylcysteine.

21 January 2018

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Inhibition of photosensitivity in erythropoietic protoporphyria with terfenadine

21 January 2018

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Fecal protoporphyrin excretion in erythropoietic protoporphyria: effect of cholestyramine and bile acid feeding

21 January 2018

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Early administration of heme arginate for acute porphyric attacks

21 January 2018

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Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysis

21 January 2018

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Sustained high plasma 5-aminolaevulinic acid concentration in a volunteer: no porphyric symptoms

21 January 2018

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A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria

21 January 2018

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Homozygous variegate porphyria: two similar cases in unrelated families.

21 January 2018

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Human delta-aminolevulinate dehydratase (ALAD) gene: structure and alternative splicing of the erythroid and housekeeping mRNAs

21 January 2018

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Assignment of human porphobilinogen deaminase to 11q24.1----q24.2 by in situ hybridization and gene dosage studies

21 January 2018

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Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12

21 January 2018

1 reference

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Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms

21 January 2018

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Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.

21 January 2018

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Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.

21 January 2018

1 reference

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Genetic aspects of erythropoietic protoporphyria

21 January 2018

1 reference

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Recessive inheritance of erythropoietic protoporphyria with liver failure

21 January 2018

1 reference

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Congenital erythropoietic porphyria: identification and expression of 10 mutations in the uroporphyrinogen III synthase gene

21 January 2018

1 reference

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10.1046/J.1365-2133.1999.02754.X

21 January 2018

Identifiers

DOI

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28 July 2017

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