Samia Tilouche

Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in <i>MT-ND2</i> and <i>MT-TL1</i> genes

Olfa Fersi Alila, Emna Rebai, Mouna Tabebi et al. · Mitochondrial DNA Part A · 2015 · 13 citations

Life Sciences, Genetics, Molecular Genetics +17

Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family

Marwa Maalej, Amel Tej, Jihène Bouguila et al. · Biochemical and Biophysical Research Communications · 2017 · 12 citations

Life Sciences, Genetics, Molecular Genetics +17

Giant cell hepatitis with autoimmune hemolytic anemia in a nine month old infant

Jihène Bouguila, Sameh Mabrouk, Samia Tilouche et al. · World Journal of Hepatology · 2013 · 10 citations · Full text

Medicine, Hematology, Pediatrics +16