A. Mrabet

Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

Hamid Azzedine, Alessandra Bolino, T. Taïeb et al. · The American Journal of Human Genetics · 2003 · 301 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Health‐related Quality of Life of People with Epilepsy Compared with a General Reference Population: A Tunisian Study

Héla Mrabet, A. Mrabet, B. Zouari et al. · Epilepsia · 2004 · 104 citations

A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset

Maria D. Lalioti, Hamish S. Scott, Pierre Genton et al. · The American Journal of Human Genetics · 1998 · 69 citations · Full text

Neurophysiology, Progressive Myoclonus Epilepsy, Neuroscience +6

Prevalence of Epilepsy in Kelibia, Tunisia

N Attia-Romdhane, A. Mrabet, M. Ben Hamida · Epilepsia · 1993 · 55 citations

High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population

Afef Achouri-Rassas, H. Khiari, S. Hadj Fredj et al. · Neurological Sciences · 2011 · 43 citations

Alzheimer's Disease, Aging, Dementia +9