Publications by authors named "Samia Menif"

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Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia.
Houyem Ouragini, Nizar Ben Halim, Sana Zitouni, Dorra Chaouachi, Imen Boudrigua, Samia Menif

Int J Neonatal Screen· November 2025

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From misconceptions to empowerment: assessing health and genetic literacy on thalassemia among Tunisian secondary school students.
Foued Maaoui, France Arboix-Calas, Ines Safra, Samia Menif, Imen Moumni

BMC Public Health· October 2025

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Circulating Erythrocyte- and Endothelial-Derived Microvesicles as Biomarkers of Hemolysis and Clinical Severity in Sickle Cell Disease.
Khouloud Khalfaoui, Mariem Chebbi, Oussema Souiai, Ilhem Ben Fraj, Monia Ben Khaled, Samia Menif

J Cell Mol Med· October 2025

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Integrating cancer education into Tunisian school curricula: A public health necessity.
Foued Maaoui, Imen Moumni, Ines Safra, Samia Menif

J Cancer Policy· September 2025

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The role of IKZF1 rs4132601 and Δ4-7 somatic deletion in acute lymphoblastic leukemia: a bioinformatics and case-control study.
Ismail Soltani, Wael Bahia, Chaker Slaymi, Hanene Gharbi, Yosra Hasni, Samia Menif

Mol Biol Rep· May 2025

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Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in Tunisia.
Houyem Ouragini, Emna Bouatrous, Manel Kasdallah, Sonia Nouira, Hamza Dallali, Samia Menif

Int J Mol Sci· May 2025

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New Born Screening of Hemoglobinopathies in a Center Tunisian Population.
Leila Chaouch, Imen Moumni, Jihene Ben Abdallah, Rim Bouchahda, Jihene Methlouthi, Samia Menif

J Pediatr Hematol Oncol· July 2024

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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, Samia Menif

Am J Perinatol· April 2024

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Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging.
Khouloud Zayoud, Asma Chikhaoui, Ichraf Kraoua, Anis Tebourbi, Dorra Najjar, Samia Menif

Cells· February 2024

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Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach.
Emna Bouatrous, Sonia Nouira, Samia Menif, Houyem Ouragini

Mol Syndromol· October 2023

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Gene 72 Arg/Pro (rs1042522) single nucleotide polymorphism increases the risk and the severity of chronic lymphocytic leukemia.
Asma Ounalli, Imen Moumni, Amal Mechaal, Aya Chakroun, Mbarka Barmat, Samia Menif

Front Oncol· October 2023

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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, Samia Menif

Ann Clin Biochem· March 2023

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Emotional and behavioral attitudes of Tunisian youth towards childhood leukemia: health education and primary prevention in perspective.
Foued Maaoui, Imen Moumni, France Arboix-Calas, Ines Safra, Samia Menif

BMC Public Health· November 2022

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Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.
Sana Zitouni, Emna Bouatrous, Ons Laabidi, Imen Boudrigua, Dorra Chaouachi, Samia Menif

Am J Perinatol· August 2022

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Hematological relevance of JAK2 V617F and calreticulin mutations in Tunisian patients with essential thrombocythemia.
Maroua Abdelghani, Haifa Hammami, Wiem Zidi, Hassiba Amouri, Hind Ben Hadj Othmen, Samia Menif

J Clin Lab Anal· August 2022

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Tyrosol Derivatives, Bearing 3,5-Disubstituted Isoxazole and 1,4-Disubstituted Triazole, as Potential Antileukemia Agents by Promoting Apoptosis.
Zaineb Abdelkafi-Koubaa, Imen Aissa, Hichem Ben Jannet, Najet Srairi-Abid, Naziha Marrakchi, Samia Menif

Molecules· August 2022

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

Cell Physiol Biochem· December 2021

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First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby.
Emna Bouatrous, Sonia Nouira, Monia Ben Khaled, Monia Ouederni, Salem Abbes, Samia Menif

J Pediatr Hematol Oncol· November 2021

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p.(V617F) mutation in Tunisian myeloproliferative neoplasms and its genotype-phenotype correlation.
Hela Sassi, Samia Menif, Safa Ben Ammar, Ahlem Farrah, Hend Ben Hadj Othmen

Pan Afr Med J· October 2021

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Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
Nawel Trabelsi, Ghada Bouguerra, Faten Haddad, Monia Ouederni, Imen Darragi, Samia Menif

Cell Physiol Biochem· March 2021

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Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.
Nawel Trabelsi, Leila Chaouch, Faten Haddad, Mouna Jaouani, Emna Barkaoui, Samia Menif

Eur J Med Genet· February 2021

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Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study.
Wael Bahia, Ismael Soltani, Anouar Abidi, Anis Haddad, Salima Ferchichi, Samia Menif

BMC Med Genomics· June 2020

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In Ph+BCR-ABL1 acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent.
Michele Baccarani, Ilaria Iacobucci, Sabina Chiaretti, Robin Foà', Poonkuzhali Balasubramanian, Samia Menif

Leukemia· March 2020

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EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients.
Amal Mechaal, Samia Menif, Salem Abbes, Ines Safra

Adv Med Sci· September 2019

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Molecular monitoring of Tunisian patients with chronic myeloid leukemia.
Samia Menif, Yosra Ben Youssef, Hatem Bellaaj, Raihane Ben Lakhal, Adnen Laatiri

Tunis Med· December 2017

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