Persistent unconjugated hyperbilirubinemia after liver transplantation due to an abnormal bilirubin UDP-glucuronosyltransferase gene promoter sequence in the donor (Q73574794)

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scientific article published on 01 July 1997

Language	Label	Description	Also known as
English	Persistent unconjugated hyperbilirubinemia after liver transplantation due to an abnormal bilirubin UDP-glucuronosyltransferase gene promoter sequence in the donor	scientific article published on 01 July 1997

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scholarly article

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5 November 2019

Persistent unconjugated hyperbilirubinemia after liver transplantation due to an abnormal bilirubin UDP-glucuronosyltransferase gene promoter sequence in the donor (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9252066%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

bilirubin metabolic disorder

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author name string

P L Jansen

1

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5 November 2019

P J Bosma

2

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5 November 2019

C Bakker

3

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5 November 2019

S P Lems

4

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5 November 2019

M J Slooff

5

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5 November 2019

E B Haagsma

6

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5 November 2019

publication date

1 July 1997

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5 November 2019

Journal of Hepatology

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5 November 2019

27

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5 November 2019

1

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5 November 2019

1-5

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5 November 2019

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome

1 reference

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7 January 2021

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Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome

1 reference

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Does Gilbert's disease exist?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2897%2980272-3

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[Prevalence of Gilbert's syndrome in Germany]

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Pathogenesis of Gilbert's syndrome

1 reference

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inferred from DOI database lookup

Gilbert's syndrome

1 reference

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Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I

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A mutation in bilirubin uridine 5'-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II

1 reference

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Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

based on heuristic

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Marked delay in indocyanine green plasma clearance with a near-normal bromosulphophthalein retention test: a constitutional abnormality?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2897%2980272-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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Ethanol increases liver uridine-diphosphate-glucuronyltransferase

1 reference

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Diagnosis of Gilbert's Syndrome: Role of Reduced Caloric Intake Test

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2897%2980272-3

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Treatment of Gilbert's syndrome with phenobarbitone.

1 reference

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Chronic administration of cyclosporin A induces a decrease in hepatic excretory function in man

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Identifiers

10.1016/S0168-8278(97)80272-3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9252066%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9252066%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

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