Mohamad A. Mikati

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 417 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +8

Effect of antiepileptic drugs on bone density in ambulatory patients

Grace Farhat, Bassem Yamout, Mohamad A. Mikati et al. · Neurology · 2002 · 360 citations

Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes

Erin L. Heinzen, Rodney A. Radtke, Thomas Urban et al. · The American Journal of Human Genetics · 2010 · 258 citations · Full text

Quinidine in the treatment of<scp>KCNT</scp>1‐positive epilepsies

Mohamad A. Mikati, Yong‐hui Jiang, Michael P. Carboni et al. · Annals of Neurology · 2015 · 220 citations · Full text

Association of Time to Treatment With Short-term Outcomes for Pediatric Patients With Refractory Convulsive Status Epilepticus

Marina Gaínza‐Lein, Iván Sánchez Fernández, Michele Jackson et al. · JAMA Neurology · 2018 · 194 citations · Full text