N-acetylation and debrisoquine hydroxylation polymorphisms in patients with Gilbert's syndrome (Q34358989)

1 August 2017

title

N-acetylation and debrisoquine hydroxylation polymorphisms in patients with Gilbert's syndrome (English)

1 reference

1 August 2017

Siegmund W

1

1 reference

1 August 2017

Fengler JD

2

1 reference

1 August 2017

Franke G

3

1 reference

1 August 2017

Zschiesche M

4

1 reference

1 August 2017

Eike O

5

1 reference

1 August 2017

Eike E

6

1 reference

1 August 2017

Meisel P

7

1 reference

1 August 2017

Wulkow R

8

1 reference

1 August 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

British Journal of Clinical Pharmacology

1 August 2017

published in

1 reference

1 August 2017

volume

32

1 reference

1 August 2017

issue

4

1 reference

1 August 2017

page(s)

467-472

1 reference

Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Constitutional hepatic dysfunction (Gilbert's disease): its natural history and related syndromes.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Analysis of bilirubin and bilirubin mono- and di-conjugates. Determination of their relative amounts in biological samples

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Positive diagnosis of Gilbert syndrome. Retrospective analysis of 59 cases with special reference to the nicotinic acid test

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Gilbert's syndrome: diagnosis by typical serum bilirubin pattern

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Genetic predisposition to bladder cancer: ability to hydroxylate debrisoquine and mephenytoin as risk factors

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Debrisoquine hydroxylation phenotype, acetylation phenotype, and ABO blood groups as genetic host factors of lung cancer risk.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Debrisoquine metabolism and genetic predisposition to lung cancer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Abnormal hepatic transport of indocyanine green in Gilbert's syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Gilbert's syndrome: evidence of morphological heterogeneity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Polymorphic acetylation and aminopyrine demethylation in Gilbert's syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Constitutional hepatic dysfunction (Gilbert's syndrome). A new definition based on kinetic studies with unconjugated radiobilirubin.

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1365-2125.1991.TB03932.X

Lung cancer risk, occupational exposure, and the debrisoquine metabolic phenotype

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368607

Metabolic oxidation phenotypes as markers for susceptibility to lung cancer

27 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1365-2125.1991.TB03932.X

Urinary glucuronic acid excretion in liver disease and the effect of a salicylamide load

21 January 2018

1 reference

12 December 2020

Antipyrine clearance in patients with Gilbert's syndrome

1 reference

12 December 2020

DEFECTS IN HEPATIC TRANSPORT OF BILIRUBIN IN CONGENITAL HYPERBILIRUBINAEMIA: AN ANALYSIS OF PLASMA BILIRUBIN DISAPPEARANCE CURVES

1 reference

12 December 2020

Normal pathways for glucuronidation, sulphation and oxidation of paracetamol in Gilbert's syndrome

1 reference

12 December 2020

[Hyperbilirubinemia in liver diseases]

1 reference

12 December 2020

A constitutional unconjugated hyperbilirubinemia combined with indocyanine green intolerance: A new functional disorder?

1 reference

12 December 2020

Glucuronide formation in patients with constitutional hepatic dysfunction (Gilbert's disease)

1 reference

12 December 2020

BILIRUBIN GLUCURONYL TRANSFERASE ACTIVITY IN LIVER DISEASE

1 reference

12 December 2020

Oxidation phenotyping with debrisoquine in Germany (East)

1 reference

12 December 2020

Debrisoquine hydroxylation polymorphism and personality

1 reference

12 December 2020

Hepatic uptake defect in patients with "Gilbert's disease"

1 reference

12 December 2020

Idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome). A study of 42 families

1 reference

12 December 2020

Defective bromosulfophthalein clearance in patients with constitutional hepatic dysfunction (Gilbert's syndrome)

1 reference

12 December 2020

N-Acetylation phenotyping with sulfamethazine--problems of sampling

1 reference

12 December 2020

[Differential diagnosis at the bedside. Harmless icterus?]

1 reference

12 December 2020

10.1111/J.1365-2125.1991.TB03932.X

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tuitejifijgezbe3fj2lseammq

30 July 2022

release_tuitejifijgezbe3fj2lseammq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tuitejifijgezbe3fj2lseammq

30 July 2022

https://api.fatcat.wiki/v0/release/tuitejifijgezbe3fj2lseammq

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/tuitejifijgezbe3fj2lseammq

1 reference

30 July 2022