Fatma Kamoun

MRI features in 17 patients with l2 hydroxyglutaric aciduria

H. Fourati, Emna Ellouze, Mourad Ahmadi et al. · European Journal of Radiology Open · 2016 · 30 citations · Full text

Medicine, Neurology, Radiology +17

A Novel Mutation in <i>FGD4/FRABIN</i> Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family

Chokri Boubaker, I. Hsairi-Guidara, Christel Castro et al. · Annals of Human Genetics · 2013 · 19 citations

Medicine, Genetics, Neurology +17

Neonatal purulent meningitis in southern Tunisia: Epidemiology, bacteriology, risk factors and prognosis

Fatma Kamoun, Mashuma Bibi Dowlut, Salma Ben Ameur et al. · Fetal and Pediatric Pathology · 2015 · 15 citations

Medicine, Microbiology, Pediatrics +17

Hemolytic Anemia and Progressive Neurologic Impairment: Think About Triosephosphate Isomerase Deficiency

Khaoula Aissa, Fatma Kamoun, L. Sfaihi et al. · Fetal and Pediatric Pathology · 2014 · 15 citations

Life Sciences, Genetics, Molecular Genetics +17

A Novel <i>MECP2</i> Gene Mutation in a Tunisian Patient with Rett Syndrome

Nourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh et al. · Genetic Testing and Molecular Biomarkers · 2009 · 14 citations

Life Sciences, Genetics, Molecular Genetics +17