Publications by authors named "Imen Boudriga"

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Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn.
Miniar Kalai, Imen Moumni, Houyem Ouragini, Dorra Chaouechi, Imen Boudriga

Am J Perinatol· April 2024

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Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)-Thalassemia among Tunisian family.
Miniar Kalai, Imen Moumni, Houyem Ouragini, Ilhem Ben Fraj, Fethi Mellouli, Imen Boudriga

Ann Clin Biochem· March 2023

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Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency.
Ghada Bouguerra, Khaoula Talbi, Nawel Trabelsi, Dorra Chaouachi, Imen Boudriga

Cell Physiol Biochem· December 2021

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Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome.
Faten Haddad, Nawel Trabelsi, Leila Chaouch, Imen Darragi, Meriem Oueslati, Imen Boudriga

Hemoglobin· March 2017

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