Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda? (Q72468695)

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26 October 2019

title

Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda? (English)

1 reference

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hepatoerythropoietic porphyria

26 October 2019

main subject

1 reference

1 reference

G. H. Elder

1

1 reference

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7 August 2023

S. G. Smith

2

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7 August 2023

C. Herrero

3

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7 August 2023

M. Lecha

4

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7 August 2023

J. M. Mascaro

5

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7 August 2023

A. M. Muniesa

6

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7 August 2023

D. B. Czarnecki

7

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7 August 2023

J. Brenan

8

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7 August 2023

V. Poulos

9

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7 August 2023

R. E. DE Salamanca

10

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7 August 2023

language of work or name

English

0 references

publication date

1 April 1981

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26 October 2019

25 April 1981

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6112327

full work available at URL

7 August 2023

https://api.elsevier.com/content/article/PII:S0140673681916159?httpAccept=text/xml

1 reference

10.1016/S0140-6736(81)91615-9

DOI

https://api.crossref.org/works/10.1016/S0140-6736(81)91615-9

https://api.elsevier.com/content/article/PII:S0140673681916159?httpAccept=text/plain

7 August 2023

1 reference

10.1016/S0140-6736(81)91615-9

DOI

https://api.crossref.org/works/10.1016/S0140-6736(81)91615-9

7 August 2023

1 reference

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26 October 2019

volume

1

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26 October 2019

issue

8226

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26 October 2019

page(s)

916-919

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Enzyme abnormalities in the porphyrias

26 October 2019

cites work

1 reference

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7 January 2021

The enzymatic defect in variegate prophyria. Studies with human cultured skin fibroblasts

1 reference

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7 January 2021

A case of biochemically unclassifiable hepatic porphyria

1 reference

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7 January 2021

Hepato-erythropoietic porphyria presenting as scleroderma and acrosclerosis in a sibling pair

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

The porphyrias and erythropoietic protoporphyria: an unusual case

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

Congenital erythropoietic porphyria with a hitherto undescribed porphyrin pattern

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

Familial and sporadic porphyria cutanea: two different diseases

1 reference

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7 January 2021

Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

The use of thin layer chromatography in the separation of free porphyrins and porphyrin methyl esters

1 reference

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7 January 2021

Studies in porphyria. IV. Expression of the gene defect of acute intermittent porphyria in cultured human skin fibroblasts and amniotic cells: prenatal diagnosis of the porphyric trait

1 reference

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7 January 2021

The prophyrins of normal human urine, with a comparison of the excretion pattern in porphyria cutanea tarda

1 reference

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7 January 2021

Porphyria Cutanea Tarda in Three Generations of a Single Family

1 reference

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7 January 2021

The inheritance of porphyria cutanea tarda

1 reference

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7 January 2021

Inheritance of porphyria cutanea tarda. Analysis of 14 cases in 5 families

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2881%2991615-9

7 January 2021

The primary enzyme defect in hereditary coproporphyria

1 reference

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7 January 2021

10.1016/S0140-6736(81)91615-9

Identifiers

DOI

1 reference

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26 October 2019

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