The cutaneous porphyrias: a review. The British Photodermatology Group. - Wikidata - awgldk - TriplyDB

The cutaneous porphyrias: a review. The British Photodermatology Group.

The cutaneous porphyrias: a review. The British Photodermatology Group.

http://www.wikidata.org/entity/Q33610809

about

Effects of visible light on the skin.Hepatoerythropoietic porphyria misdiagnosed as child abuse: cutaneous, arthritic, and hematologic manifestations in siblings with a novel UROD mutation.Therapy of porphyria cutanea tarda.Erythropoietic protoporphyria without skin symptoms-you do not always see what they feel 66-year-old woman with painless vesicular lesions.Liver cirrhosis induced by porphyria cutanea tarda: a case report and review Cutaneous porphyrias part I: epidemiology, pathogenesis, presentation, diagnosis, and histopathology.Mitochondrial dysfunction: a neglected component of skin diseases.Severe neonatal congenital erythropoietic porphyria.Colon perforation secondary to porphyria.A method to assess the protective efficacy of sunscreens against visible light-induced pigmentation.

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P2860

The cutaneous porphyrias: a review. The British Photodermatology Group.

http://www.wikidata.org/entity/Q33610809

description

1999 nî lūn-bûn

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1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի ապրիլին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

The cutaneous porphyrias: a review. The British Photodermatology Group.

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The cutaneous porphyrias: a review. The British Photodermatology Group.

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The cutaneous porphyrias: a review. The British Photodermatology Group.

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The cutaneous porphyrias: a review. The British Photodermatology Group.

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The cutaneous porphyrias: a review. The British Photodermatology Group.

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The cutaneous porphyrias: a review. The British Photodermatology Group.

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British Journal of Dermatology

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The cutaneous porphyrias: a review. The British Photodermatology Group.

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Murphy GM

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P2860

Recessive inheritance of erythropoietic protoporphyria with liver failure

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

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

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

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

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

Discoid lupus erythematosus and porphyria cutanea tarda

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

Early administration of heme arginate for acute porphyric attacks.

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

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573-581

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