Fakhri Kallabi

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome

Fakhri Kallabi, Neila Belghuith, Hajer Aloulou et al. · Archives of Medical Research · 2016 · 27 citations

Allelic Variant, Mendelian Disorder, Genetic Disorder +12

Polymorphisms of glutathione S-transferases M1, T1, P1 and A1 genes in the Tunisian population: An intra and interethnic comparative approach

Ghada Ben Salah, Fakhri Kallabi, S. Maatoug et al. · Gene · 2012 · 24 citations

Genetic Determinant, Glutathione S-transferases M1, Biochemistry +9

A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy

Mouna Tabebi, Emna Mkaouar‐Rebai, Mouna Mnif et al. · Biochemical and Biophysical Research Communications · 2015 · 23 citations

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +14

Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation

Mouna Tabebi, Nadia Charfi, Fakhri Kallabi et al. · Journal of Diabetes and its Complications · 2016 · 18 citations

Mendelian Disorder, Ophthalmology, Genetic Disorder +10

Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect

Bochra Ben Rhouma, Fakhri Kallabi, Nadia Mahfoudh et al. · The Journal of Steroid Biochemistry and Molecular Biology · 2016 · 13 citations

Novel Cases, Genetic Disorder, Genetics +9