New type of hepatic porphyria with porphobilinogen synthase defect and intermittent acute clinical manifestation.
about
delta-Aminolevulinate dehydratase deficient porphyria: identification of the molecular lesions in a severely affected homozygoteHuman delta-aminolevulinate dehydratase: nucleotide sequence of a full-length cDNA cloneMolecular characterization of the human delta-aminolevulinate dehydratase 2 (ALAD2) allele: implications for molecular screening of individuals for genetic susceptibility to lead poisoningThe schiff base complex of yeast 5-aminolaevulinic acid dehydratase with laevulinic acidThe X-ray structure of yeast 5-aminolaevulinic acid dehydratase complexed with two diacid inhibitorsX-ray structure of a putative reaction intermediate of 5-aminolaevulinic acid dehydrataseComparative studies on the 5-aminolaevulinic acid dehydratases from Pisum sativum, Escherichia coli and Saccharomyces cerevisiae.Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetoneThe cutaneous porphyrias: a review. The British Photodermatology Group.Assignment of the human gene for delta aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassay.Clinically important features of porphyrin and heme metabolism and the porphyrias.Influence of the common human delta-aminolevulinate dehydratase polymorphism on lead body burdenA LC-MS/MS method for the specific, sensitive, and simultaneous quantification of 5-aminolevulinic acid and porphobilinogen.Dual porphyrias revisited.Porphyrin and heme metabolism and the porphyrias.Treatment of the porphyrias.Urinary 5-aminolevulinic acid in lead-exposed children.Plumboporphyria (ALAD deficiency) in a lead worker: a scenario for potential diagnostic confusionDirect assay of delta-aminolevulinic acid dehydratase in heme biosynthesis for the detection of porphyrias by tandem mass spectrometryDrugs and porphyria.Acute hepatic porphyrias: Recommendations for evaluation and long-term management.Structural studies of substrate and product complexes of 5-aminolaevulinic acid dehydratase from humans, Escherichia coli and the hyperthermophile Pyrobaculum calidifontis.Scientific Opinion on Lead in Food
P2860
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P2860
New type of hepatic porphyria with porphobilinogen synthase defect and intermittent acute clinical manifestation.
description
1979 nî lūn-bûn
@nan
1979 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1979 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
name
New type of hepatic porphyria ...... acute clinical manifestation.
@ast
New type of hepatic porphyria ...... acute clinical manifestation.
@en
New type of hepatic porphyria ...... acute clinical manifestation.
@nl
type
label
New type of hepatic porphyria ...... acute clinical manifestation.
@ast
New type of hepatic porphyria ...... acute clinical manifestation.
@en
New type of hepatic porphyria ...... acute clinical manifestation.
@nl
prefLabel
New type of hepatic porphyria ...... acute clinical manifestation.
@ast
New type of hepatic porphyria ...... acute clinical manifestation.
@en
New type of hepatic porphyria ...... acute clinical manifestation.
@nl
P2093
P356
P1476
New type of hepatic porphyria ...... acute clinical manifestation.
@en
P2093
J Schneider
R von Tiepermann
P304
P356
10.1007/BF01481493
P577
1979-10-01T00:00:00Z