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Medicine|June 27, 2026
Molecular profiling of coronary stent testenosis: A systematic review and functional analysis of implicated genesRajaa El Mansouri, Rachida Habbal, Hind Dehbi
The Journal of International Medical Research|July 27, 2023
A novel SCN8A variant of unknown significance in pediatric epilepsy: a case reportWafaa Bouzroud, Amal Tazzite, Ikhlass Boussakri, et al.
DNA and Cell Biology|August 13, 2013
Genotype variability and haplotype frequency of MDR1 (ABCB1) gene polymorphism in MoroccoYaya Kassogue, Hind Dehbi, Sanaa Nassereddine, et al.
Clinical Pathology (Thousand Oaks, Ventura County, Calif.)|September 23, 2022
R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case ReportWafaa Bouzroud, Amal Tazzite, Sarah Berrada, et al.
Cureus|August 1, 2025
Molecular Aspects of Rare Coagulation Factor DeficienciesHajar Tourbih, Asma Harrach, Hanaa Bencharef, et al.
European Journal of Ophthalmology|May 22, 2021
Meta-analysis of CYP1B1 gene mutations in primary congenital glaucoma patientsAmine Haddad, Oum Kaltoum Ait Boujmia, Loubna El Maaloum, et al.
Springerplus|May 14, 2015
Association of glutathione S-transferase (GSTM1 and GSTT1) genes with chronic myeloid leukemiaYaya Kassogue, Hind Dehbi, Meryem Quachouh, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|July 27, 2020
Association of Multidrug Resistance Gene-1 (MDR1 C1236T) Polymorphism with the Risk of Acute Myeloid Leukemia in a Moroccan PopulationOum Kaltoum Ait Boujmia, Sellama Nadifi, Hind Dehbi, et al.
Medical Oncology (Northwood, London, England)|December 3, 2013
Functional polymorphism of CYP2B6 G15631T is associated with hematologic and cytogenetic response in chronic myeloid leukemia patients treated with imatinibYaya Kassogue, Meryem Quachouh, Hind Dehbi, et al.
Current Research in Translational Medicine|September 11, 2020
The influence of DNMT3A and DNMT3B gene polymorphisms on acute myeloid leukemia risk in a Moroccan populationOum Kaltoum Ait Boujmia, Sellama Nadifi, Hind Dehbi, et al.
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