Asma Ammar

Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function

Caroline Huzé, Stéphanie Bauché, Pascale Richard et al. · The American Journal of Human Genetics · 2009 · 166 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

Asma Ammar, François Petit, Nektaria Alexandri et al. · Journal of Neurology · 2009 · 78 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Specialty choices of medical students and house officers in Karachi, Pakistan

Mehwish Aslam, Arif Ali, Tahir Taj et al. · Eastern Mediterranean Health Journal · 2011 · 49 citations · Full text

Nursing, Family Medicine, Primary Care +13

A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia

Asma Ammar, Payam Soltanzadeh, Stéphanie Bauché et al. · PLoS ONE · 2013 · 48 citations · Full text

Muscle Function, Genetics, Molecular Genetics +16

The <i>CHRNE</i> 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

Pascale Richard, Karen Gaudon, Asma Ammar et al. · Neurology · 2008 · 41 citations