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The porphyrias
scientific article published on 01 April 2002
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
review article
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stated in
Europe PubMed Central
title
The porphyrias
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
author name string
Shigeru Sassa
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
publication date
1 April 2002
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Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
published in
Photodermatology, Photoimmunology and Photomedicine
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Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
volume
18
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Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
page(s)
56-67
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
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Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone
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Highly heterogeneous nature of delta-aminolevulinate dehydratase (ALAD) deficiencies in ALAD porphyria
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New type of acute porphyria with porphobilinogen synthase (delta-aminolevulinic acid dehydratase) defect in the homozygous state
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Novel molecular defects of the delta-aminolevulinate dehydratase gene in a patient with inherited acute hepatic porphyria
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Cloning and expression of the defective genes from a patient with delta-aminolevulinate dehydratase porphyria
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Alterations in haem biosynthesis during the human menstrual cycle: studies in normal subjects and patients with latent and active acute intermittent porphyria
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Acute intermittent porphyria: effect of diet and griseofulvin
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FACTORS AFFECTING THE EXCRETION OF PORPHYRIN PRECURSORS BY PATIENTS WITH ACUTE INTERMITTENT PORPHYRIA. I. THE EFFECT OF DIET
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A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria
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Crossref
reference URL
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7 January 2021
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Uroporphyrinogen III synthase. An alternative promoter controls erythroid-specific expression in the murine gene
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Crossref
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7 January 2021
based on heuristic
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Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene
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Familial and sporadic porphyria cutanea: two different diseases.
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Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda
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Crossref
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7 January 2021
based on heuristic
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Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patients
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
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7 January 2021
based on heuristic
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Porphyria cutanea tarda. Clinical features and laboratory findings in 40 patients
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association
1 reference
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Crossref
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7 January 2021
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Porphyria cutanea tarda associated with the acquired immune deficiency syndrome
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Crossref
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7 January 2021
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Ascorbic acid deficiency in porphyria cutanea tarda
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7 January 2021
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Liposoluble vitamins and naturally occurring carotenoids in porphyria cutanea tarda
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7 January 2021
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Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
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Porphyria cutanea tarda, hepatitis C, and HFE gene mutations in North America
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7 January 2021
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Activation of the complement system in patients with porphyrias after irradiation in vivo
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7 January 2021
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Photodynamic action of uroporphyrin on the complement system in porphyria cutanea tarda
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
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Activation of complement by 405-nm light in serum from porphyria cutanea tarda
1 reference
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7 January 2021
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Complement cleavage products in the phototoxic reaction of porphyria cutanea tarda
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyria cutanea tarda and human immunodeficiency virus infection
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recovery from porphyria cutanea tarda with no specific therapy other than avoidance of hepatic toxins
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
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7 January 2021
based on heuristic
inferred from DOI database lookup
[General symptoms of late skin porphyria (porphyria cutanea tarda) as an indication for its treatment.]
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effect of chloroquine on hepatic uroporphyrin metabolism in patients with porphyria cutanea tarda.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatoerythropoietic porphyria: clinical, biochemical, and enzymatic studies in a three-generation family lineage
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassay
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uroporphyrinogen decarboxylase: a splice site mutation causes the deletion of exon 6 in multiple families with porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial porphyria cutanea tarda: characterization of seven novel uroporphyrinogen decarboxylase mutations and frequency of common hemochromatosis alleles
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of uroporphyrinogen decarboxylase complementary DNAs in sporadic porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous case of hereditary coproporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary coproporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Harderoporphyria: a variant hereditary coproporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical and biochemical features of variegate porphyria: an analysis of 300 cases studied at Groote Schuur Hospital, Cape Town
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous variegate porphyria: two similar cases in unrelated families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous variegate porphyria. A severe skin disease of infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous variegate porphyria: identification of mutations on both alleles of the protoporphyrinogen oxidase gene in a severely affected proband
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a new mutation responsible for hepatoerythropoietic porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure of the human ferrochelatase gene. Exon/intron gene organization and location of the gene to chromosome 18.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyrins and related compounds as photodynamic sensitizers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systemic photoprotection.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Zinc as an oral photoprotective agent in erythropoietic protoporphyria?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1600-0781.2002.180202.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1034/J.1600-0781.2002.180202.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
PubMed publication ID
12147038
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12147038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12147038%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
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