Ridha Mrad

Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation

Frédéric Laumonnier, Sébastien Roger, Pascaline Guérin et al. · American Journal of Psychiatry · 2006 · 166 citations · Full text

A Homozygous Splice Mutation in the<i>HSF4</i>Gene Is Associated with an Autosomal Recessive Congenital Cataract

Nizar Smaoui, O. Beltaief, Sonia Benhamed et al. · Investigative Ophthalmology & Visual Science · 2004 · 99 citations

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 <i>UBE3A</i> truncating mutation in large Tunisian Angelman syndrome pedigree

Leila Abaied, Médiha Trabelsi, M Chaâbouni et al. · American Journal of Medical Genetics Part A · 2009 · 77 citations

Quality-of-Life Research on the Internet: Feasibility and Potential Biases in Patients with Ulcerative Colitis

Roy Soetikno, Ridha Mrad, Vivian Y Pao et al. · Journal of the American Medical Informatics Association · 1997 · 72 citations · Full text