(Q35008630)

5 August 2017

title

Prevalence of Gilbert syndrome in parents of neonates with pathologic indirect hyperbilirubinemia (English)

1 reference

bilirubin metabolic disorder

5 August 2017

main subject

1 reference

1 reference

Forough Saki

1

1 reference

ORCID Public Data File 2021

author name string

Fariba Hemmati

series ordinal

2

1 reference

5 August 2017

Mahmoud Haghighat

series ordinal

3

1 reference

5 August 2017

language of work or name

1 reference

1 March 2011

1 reference

5 August 2017

published in

Annals of Saudi Medicine

1 reference

5 August 2017

volume

31

1 reference

5 August 2017

issue

2

1 reference

5 August 2017

page(s)

140-144

1 reference

Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus

5 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=3102472

Gilbert syndrome accelerates development of neonatal jaundice

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3102472

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3102472

The utility of rifampin in diagnosing Gilbert's syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3102472

Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3102472

Genetic testing for Gilbert's syndrome: how useful is it in determining the cause of jaundice?

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3102472

Neonatal hyperbilirubinemia and Gilbert's syndrome

26 October 2018

1 reference

12 December 2020

RhD Hemolytic Disease of the Newborn

1 reference

12 December 2020

Role of overnight rifampin test in diagnosing Gilbert's syndrome

1 reference

12 December 2020

Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates

1 reference

12 December 2020

Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn

1 reference

12 December 2020

[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice]

1 reference

12 December 2020

Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates

1 reference

12 December 2020

Analyses of polymorphism for UGT1*1 exon 1 promoter in neonates with pathologic and prolonged jaundice

1 reference

12 December 2020

Identifiers

DOI

10.4103/0256-4947.77498

1 reference

release_2itfs4rihvfxppz2uzkphx243i

5 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2itfs4rihvfxppz2uzkphx243i

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3102472

1 reference

5 August 2017

1 reference