Lamia Ben Jemâa

Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation

Maher Kharrat, Véronique Tardy, Ridha Mrad et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 88 citations

Mendelian Disorder, Congenital Adrenal Hyperplasia, Cyp21 Active Gene +14

A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric features

Imen Rejeb, Yoann Saillour, L. Castelnau et al. · European Journal of Human Genetics · 2008 · 41 citations · Full text

Developmental Anomaly, Novel Splice Mutation, Pak3 Gene +10

MEFV Mutations in Tunisian Patients Suffering from Familial Mediterranean Fever

Habiba Chaâbouni, Mohamed Ksantini, Ridha Mrad et al. · Seminars in Arthritis and Rheumatism · 2007 · 39 citations

Diagnostic Virology, Mendelian Disorder, Pathogenesis +7

Performance limitations in the robust servomechanism problem for discrete-time lti systems

Lamia Ben Jemâa, E.J. Davison · IEEE Transactions on Automatic Control · 2003 · 39 citations

Engineering, Sampled System, Robust Control +18

Mosaic parental germline mutations causing recurrent forms of malformations of cortical development

Julia Lauer Zillhardt, Karine Poirier, Loïc Broix et al. · European Journal of Human Genetics · 2015 · 35 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +13