Publications by authors named "Miniar Kalai"

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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

Ann Clin Biochem· March 2023

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New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level.
Leila Chaouch, Houssem Sellami, Miniar Kalai, Imen Darragi, Imen Boudrigua

J Pediatr Hematol Oncol· January 2020

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The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.
Miniar Kalai, Marwa Dridi, Leila Chaouch, Imen Moumni, Houyem Ouragini

Hematology· April 2017

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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Leila Chaouch, Imen Moumni, Houyem Ouragini, Imen Darragi, Miniar Kalai

Hematology· August 2016

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Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.
Leila Chaouch, Miniar Kalai, Dorra Chaouachi, Fethi Mallouli, Raouf Hafsia

Tunis Med· April 2015

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Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients.
Leila Chaouch, Miniar Kalai, Manel Ben Jbara, Arij Ben Chaabene, Imen Darragi

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub· March 2015

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Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.
Leila Chaouch, Emna Talbi, Imen Moumni, Arij Ben Chaabene, Miniar Kalai

Dis Markers· June 2014

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Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene.
Leila Chaouch, Emna Talbi, Imen Moumni, Arij Ben Chaabene, Miniar Kalai

Dis Markers· April 2013

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