(Q40150902)

18 September 2017

1 reference

title

Recent advances in the identification of enzyme deficiencies in the porphyrias (English)

1 reference

oxidoreductases acting on CH-CH group donors

18 September 2017

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6344903

4 October 2023

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

4 October 2023

author name string

G. H. Elder

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6344903

4 October 2023

language of work or name

English

0 references

publication date

1 June 1983

1 reference

full work available at URL

18 September 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2133.1983.tb01088.x

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.1983.tb01088.x/fullpdf

4 October 2023

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

British Journal of Dermatology

4 October 2023

published in

1 reference

18 September 2017

volume

108

1 reference

18 September 2017

issue

6

1 reference

18 September 2017

page(s)

729-734

1 reference

Biosynthesis of the pigments of life: formation of the macrocycle

18 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.1983.TB01088.X

Familial and sporadic porphyria cutanea: two different diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.1983.TB01088.X

Characterization of the porphobilinogen deaminase deficiency in acute intermittent porphyria. Immunologic evidence for heterogeneity of the genetic defect

21 January 2018

1

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts

4 October 2023

3

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Neurologic manifestations of acute porphyria

4 October 2023

4

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

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

4 October 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

The inherited enzymatic defect in porphyria variegata

4 October 2023

6

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

New type of acute porphyria with porphobilinogen synthase (delta-aminolevulinic acid dehydratase) defect in the homozygous state

4 October 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda

4 October 2023

9

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase

4 October 2023

10

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

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

4 October 2023

11

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Decreased hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda

4 October 2023

12

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Homozygous case of hereditary coproporphyria

4 October 2023

14

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria

4 October 2023

15

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

The enzymatic defect in porphyria cutanea tarda

4 October 2023

16

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

The UPS locus encoding uroporphyrinogen I synthase is located on human chromosome 11

4 October 2023

18

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Congenital erythropoietic porphyria

4 October 2023

19

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Harderoporphyria: a variant hereditary coproporphyria

4 October 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

The development and prognosis of chronic intoxication by tetrachlordibenzo-p-dioxin in men

4 October 2023

21

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Studies in porphyria: functional evidence for a partial deficiency of ferrochelatase activity in mitogen-stimulated lymphocytes from patients with erythropoietic protoporphyria

4 October 2023

24

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Enzymatic defects in porphyria: an overview

4 October 2023

25

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Heme biosynthesis in intermittent acute prophyria: decreased hepatic conversion of porphobilinogen to porphyrins and increased delta aminolevulinic acid synthetase activity

4 October 2023

27

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

Uroporphyrin I stimulation of collagen biosynthesis in human skin fibroblasts. A unique dark effect of porphyrin

4 October 2023

28

1 reference

https://api.crossref.org/works/10.1111/J.1365-2133.1983.TB01088.X

4 October 2023

Identifiers

1 reference

18 September 2017

1 reference