Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.

British journal of haematology - 1 Dec 2001

Galanello R, Piras S, Barella S, Leoni G B, Cipollina M D, Perseu L, Cao A

Abstract excerpt

Cholelithiasis has been reported with a variable incidence in homozygous beta-thalassaemia, the reasons for which have only partially been defined. Disease-associated factors or specific modifier genes may be implicated. We assessed the prevalence of cholelithiasis and the effect of co-inherited Gilbert's syndrome genotype on its development in 261 thalassaemia major (TM) and 35 thalassaemia intermedia (TI)...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to beta-Thalassemia
Share to Cholelithiasis
Share to Gilbert Disease

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucuronosyltransferase

Share to Homozygote

Share to Incidence

Share to Promoter Regions, Genetic

Share to TATA Box

Source

Identifiers

PMID: 11843828
DOI: 10.1046/j.1365-2141.2001.03200.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.PMID 11843828Read ↗

Cholelithiasis in thalassemia major.Semantic proximity Read ↗

Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.Semantic proximity Read ↗

Thalassemia minor, the Gilbert mutation, and the risk of gallstones.Semantic proximity Read ↗

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.Semantic proximity Read ↗

Association between promoter and coding region mutations of UDP-glucuronosyltransferase 1A1 and beta-thalassemia/Hb E with cholelithiasis.Semantic proximity Read ↗

UGT1A1 (TA)n genotype is not the major risk factor of cholelithiasis in sickle cell disease children.Semantic proximity Read ↗

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.Semantic proximity Read ↗

Coinheritance of Gilbert Syndrome Increases the Risk for Developing Gallstones in Patients With Hereditary SpherocytosisSemantic proximity Read ↗

The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.Semantic proximity Read ↗

Influence of UGT1A1 promoter polymorphism, α-thalassemia and βs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.Semantic proximity Read ↗

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.Semantic proximity Read ↗

Gilbert syndrome associated with beta-thalassemia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.