Leila Chaouch

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 16 publications

Mutation Spectrum of Hemoglobinopathies in Tunisia.

Mutation Spectrum of Hemoglobinopathies in Tunisia.

Journal: Human mutation

Published: November 28, 2025

New Born Screening of Hemoglobinopathies in a Center Tunisian Population.

New Born Screening of Hemoglobinopathies in a Center Tunisian Population.

Journal: Journal of pediatric hematology/oncology

Published: November 21, 2023

Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.

Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.

Journal: European journal of medical genetics

Published: March 01, 2020

New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level.

New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level.

Journal: Journal of pediatric hematology/oncology

Published: November 06, 2019

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.

Journal: Hemoglobin

Published: June 09, 2017

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.

Journal: Hematology (Amsterdam, Netherlands)

Published: November 22, 2016

Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene.

Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene.

Journal: International journal of laboratory hematology

Published: August 01, 2016

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.

Journal: Hematology (Amsterdam, Netherlands)

Published: April 15, 2016

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

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

Journal: La Tunisie medicale

Published: September 17, 2015

Genetic polymorphism of cytochrome P450 2E1 and the risk of nasopharyngeal carcinoma

Genetic polymorphism of cytochrome P450 2E1 and the risk of nasopharyngeal carcinoma

Journal: Bulletin du cancer

Published: September 12, 2015

Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.

Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.

Journal: Hematology (Amsterdam, Netherlands)

Published: July 07, 2015

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia.

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia.

Journal: Polish journal of pathology : official journal of the Polish Society of Pathologists

Published: August 01, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026