Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients
Author:
Affiliation:
1. National Institute of Immunohaematology (ICMR)K.E.M. Hospital Campus, Parel, India
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1179/1607845413Y.0000000142
Reference25 articles.
1. Eponym
2. Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database
3. UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease
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1. Gilbert syndrome in patients with inherited hemolytic anemia modifies the clinical phenotype;Pediatric Hematology Oncology Journal;2024-06
2. A systemic review of association between UDP glucuronosyltransferase family 1 member A1 (UGT1A1) polymorphisms in Gilbert's syndrome in Sickle Cell Disease;Journal of Clinical and Scientific Research;2022
3. Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia;European Journal of Medical Genetics;2021-02
4. A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia;Annals of Hematology;2020-07-16
5. Gilbert’s Syndrome in Children with Unconjugated Hyperbilirubinemia – An Analysis of 170 Cases;The Indian Journal of Pediatrics;2020-03-27
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