Lamia Boughamoura

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients

Leila Ben-Khemis, Najla Mekki, Imen Ben‐Mustapha et al. · Molecular Immunology · 2017 · 35 citations

Founder Mutation, Genetic Disorder, Genetics +8

Epidemiology and clinical profile of pathogens responsible for the hospitalization of children in Sousse area, Tunisia

Inès Brini, Aida Guerrero, Naïla Hannachi et al. · PLoS ONE · 2017 · 27 citations · Full text

Clinical Symptoms, Respiratory Virus Immunity, Malaria +26

Demographic and seasonal characteristics of respiratory pathogens in neonates and infants aged 0 to 12 months in the Central‐East region of Tunisia

Inès Brini, Naïla Hannachi, Aida Guerrero et al. · Journal of Medical Virology · 2018 · 23 citations · Full text

Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele

Rahma Mani, Sabrina Belkacem, Zohra Soua et al. · Human Mutation · 2019 · 23 citations

Genetics, Genetic Epidemiology, Diagnosis +16

Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in Tunisia

A. Jelassi, Imen Jguirim, Mohamed Najah et al. · Atherosclerosis · 2008 · 21 citations

Limited Mutational Heterogeneity, Familial Hypercholesterolemia, Lipid Disorder +9