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Hematology Volume 19, 2014 - Issue 7
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Thalassemia

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients

Pooja S. DabkeNational Institute of Immunohaematology (ICMR)K.E.M. Hospital Campus, Parel, India
,
Roshan B. ColahNational Institute of Immunohaematology (ICMR)K.E.M. Hospital Campus, Parel, India
,
Kanjaksha K. GhoshNational Institute of Immunohaematology (ICMR)K.E.M. Hospital Campus, Parel, India
&
Anita H. NadkarniNational Institute of Immunohaematology (ICMR)K.E.M. Hospital Campus, Parel, IndiaCorrespondence[email protected]
Pages 388-392 | Published online: 30 Nov 2013

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Faten Haddad, Nawel Trabelsi, Leila Chaouch, Imen Darragi, Meriem Oueslati, Imen Boudriga, Dorra Chaouachi, Wijdene El-Borgi, Raouf Hafsia, Salem Abbes & Houyem Ouragini. (2017) Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome. Hemoglobin 41:2, pages 147-150.
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Yang Deming, An Qingcong & Liu Yonggang. (2016) Molecular cloning, sequence identification and expression profile of domestic guinea pig (Cavia porcellus) UGT1A1 gene. Biotechnology & Biotechnological Equipment 30:1, pages 106-111.
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Articles from other publishers (4)

Sanya Sachdeva, Ragini Bodade & Anand Bodade. (2022) 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 11:2, pages 99.
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Nawel Trabelsi, Leila Chaouch, Faten Haddad, Mouna Jaouani, Emna Barkaoui, Imen Darragi, Dorra Chaouachi, Imen Boudrigua, Samia Menif & Salem Abbes. (2021) Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia. European Journal of Medical Genetics 64:2, pages 104139.
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Vikrant Sood, Bikrant Bihari Lal, Shvetank Sharma, Rajeev Khanna, Manish K. Siloliya & Seema Alam. (2020) Gilbert’s Syndrome in Children with Unconjugated Hyperbilirubinemia – An Analysis of 170 Cases. The Indian Journal of Pediatrics 88:2, pages 154-157.
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Hui Yang, Qian Wang, Lei Zheng, Xiang-bin Zheng, Min Lin, Xiao-Fen Zhan & Li-Ye Yang. (2016) Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia. Pediatrics & Neonatology 57:4, pages 310-317.
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