Ibtihel Benhaj Mbarek

Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria

Ibtihel Benhaj Mbarek, Saoussen Abroug, Asma Omezzine et al. · BMC Nephrology · 2011 · 26 citations · Full text

Novel mutations in steroid-resistant nephrotic syndrome diagnosed in Tunisian children

Ibtihel Benhaj Mbarek, Saoussen Abroug, Asma Omezzine et al. · Pediatric Nephrology · 2010 · 21 citations

Tunisian Children, Mendelian Disorder, Genetic Disorder +8

<i>HOGA1</i> Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients

Saoussen M'dimegh, Cécile Aquaviva‐bourdain, Asma Omezzine et al. · Journal of Clinical Laboratory Analysis · 2016 · 16 citations · Full text

Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1

Saoussen M'dimegh, Asma Omezzine, Ibtihel Benhaj Mbarek et al. · Annals of Human Genetics · 2016 · 14 citations

Unusual clinical outcome of primary Hyperoxaluria type 1 in Tunisian patients carrying 33_34InsC mutation

Ibtihel Benhaj Mbarek, Saoussen Mdimeg, Amira Moussa et al. · BMC Nephrology · 2017 · 13 citations · Full text