Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q35960831)
Watch
English
Hepatic porphyrias.
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Hepatic porphyrias
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
author
David A. Brenner
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
author name string
Y V Scarlett
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
J R Bloomer
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
publication date
1 February 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
published in
Clinics in liver disease
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
volume
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
page(s)
77-102, vi
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
cites work
Biogenesis of embryonic chick liver delta-aminolevulinate synthase: regulation of the level of mRNA by hemin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of antihypertensive drugs on hepatic heme biosynthesis, and evaluation of ferrochelatase inhibitors to simplify testing of drugs for heme pathway induction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acute peripheral neuropathy due to hereditary coproporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
δ‐aminolevulinate dehydrase: a new genetic polymorphism in man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Catecholamine uptake, accumulation, and release in acute porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human delta-aminolevulinate synthase: assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of deficient heme synthase activity in protoporphyria with cultured skin fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The liver in protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatic disease in erythropoietic protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver transplantation in a patient with protoporphyria.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal liver failure in protoporphyria. Synergism between ethanol excess and the genetic defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative effects of glycerol and dextrose on porphyrin precursor excretion in acute intermittent porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Seizure management in acute hepatic porphyria: risks of valproate and clonazepam
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The enzymatic defect in variegate prophyria. Studies with human cultured skin fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The pathology of the liver in porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human erythroid 5-aminolevulinate synthase: promoter analysis and identification of an iron-responsive element in the mRNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decreased Haem Synthetase Activity in Blood Cells of Patients with Erythropoietic Protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatitis C virus antibodies and liver disease in patients with porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Erythropoietic protoporphyria 10 years experience
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial location of protoporphyrinogen oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Harderoporphyrin coproporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acute hepatic porphyria syndrome with porphobilinogen synthase defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence that the coproporphyrinogen oxidase activity of rat liver is situated in the intermembrane space of mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acquired porphyria cutanea tarda, primary refractory anemia, and hepatic siderosis. Report of a case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial localization of coproporphyrinogen III oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific splicing mutation in acute intermittent porphyria.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the human coproporphyrinogen oxidase to chromosome 9
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanism of allylisopropylacetamide-induced increase of -aminolevulinate synthetase in liver mitochondria. V. Mechanism of regulation by hemin of the level of -aminolevulinate synthetase in rat liver mitochondria.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Four novel mutations in the ferrochelatase gene among erythropoietic protoporphyria patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Erythropoietic protoporphyria: unusual skin and neurological problems after liver transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is hepatitis C virus infection a trigger of porphyria cutanea tarda?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatoerythropoietic porphyria precipitated by viral hepatitis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the ferrochelatase gene associated with erythropoietic protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and expression of the defective genes from a patient with delta-aminolevulinate dehydratase porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Demonstration of intracytoplasmic needle-like inclusions in hepatocytes of patients with porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The structural organization of haem synthesis in rat liver mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MRI reveals multiple reversible cerebral lesions in an attack of acute intermittent porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The regulation of tryptophan pyrrolase activity by tryptophan
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HOMOZYGOUS VARIEGATE PORPHYRIA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of complement in porphyrin-induced photosensitivity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatoerythropoietic porphyria: a variant of childhood-onset porphyria cutanea tarda. Porphyrin profiles and enzymatic studies of two cases in a family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential effects of protoporphyrin and uroporphyrin on murine mast cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bile porphyrin analysis in the evaluation of variegate porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of latent variegate porphyria by fluorescence emission spectroscopy of plasma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of the ferrochelatase gene in a patient with protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Grand mal seizures and acute intermittent porphyria. The problem of differential diagnosis and treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyric neuropathy and hereditary delta-aminolevulinic acid dehydratase deficiency in an adult
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
International review of drugs in acute porphyria--1980.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for two uroporphyrinogen decarboxylase isoenzymes in human erythrocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular defect in human erythropoietic protoporphyria with fatal liver failure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of human porphobilinogen deaminase to 11q24.1----q24.2 by in situ hybridization and gene dosage studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is porphyria cutanea tarda a risk factor in the development of hepatocellular carcinoma? A case report and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acute intermittent porphyria. New morphologic and biochemical findings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyria: theories of etiology and treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyria and hepatocellular carcinoma.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human protoporphyria: reduced cutaneous photosensitivity and lower erythrocyte porphyrin levels during pregnancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human delta-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of delta-aminolevulinate synthase in avian cells: separate genes encode erythroid-specific and nonspecific isozymes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Induction of hepatic delta-amino-levulinic acid synthetase by oral contraceptive steroids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure of the gene for human uroporphyrinogen decarboxylase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular characterization of a ferrochelatase gene defect causing anomalous RNA splicing in erythropoietic protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recessive inheritance of erythropoietic protoporphyria with liver failure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyrin content of bone marrow and liver in the various forms of porphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human ferrochelatase: a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Soluble hepatic delta-aminolevulinic acid synthetase: end-product inhibition of the partially purified enzyme
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acute intermittent porphyria caused by a C----T mutation that produces a stop codon in the porphobilinogen deaminase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Central-nervous-system effects of ingestin of L-tryptophan by normal subjects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal iron and water metabolism in acute intermittent porphyria with new morphologic findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High prevalence of intermittent acute porphyria in a psychiatric patient population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
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/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The porphyrias as inborn errors of metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of the variegate porphyria (VP) gene: contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Porphyria variegata and porphyria cutanea tarda in siblings: chemical and genetic aspects (addendum)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic aspects of erythropoietic protoporphyria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regulation of synthesis and intracellular translocation of δ-aminolevulinate synthase by heme and its relation to the heme saturation of tryptophan pyrrolase in rat liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanism and stereochemistry of the 5-aminolaevulinate synthetase reaction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970365-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1089-3261(05)70365-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
PubMed publication ID
15560047
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15560047
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15560047%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 January 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit