Labiba Adala

An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation

Moez Gribaa, M. Younès, Yosra Bouyacoub et al. · Journal of Bone and Mineral Metabolism · 2009 · 57 citations

Mendelian Disorder, Genetic Disorder, Genetics +6

Placental Mesenchymal Dysplasia with Beckwith–Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines

D. Hmida, Moez Gribaa, Tahar Yacoubi et al. · Placenta · 2008 · 44 citations

Developmental Anomaly, Developmental Biology, Dysplasia +15

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients

Abdelbasset Amara, Labiba Adala, Ilhem Ben Charfeddine et al. · European Journal of Paediatric Neurology · 2011 · 38 citations

Genetic Disorder, Medicine, Genetics +9

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

A. Mili, Ilhem Ben Charfeddine, Ons Mamaï et al. · Journal of Human Genetics · 2011 · 27 citations · Full text

Glycoproteomics, Biochemistry, Natural Sciences +11

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family

Ilhem Ben Charfeddine, Felix G. Riepe, N. Kahloul et al. · General and Comparative Endocrinology · 2011 · 23 citations

Adrenal Gland, Urology, Novel Cyp11b1 Mutations +10