Akarsu, E. O. Et Al. 2016. Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.42 , 49-51.

Akarsu, E. O., Tekturk, P., Yapici, Z., Tepgec, F., Uyguner, Z. O., & Baykan, B., (2016). Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.42, 49-51.

Akarsu, Emel Et Al. "Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation," SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.42, 49-51, 2016

Akarsu, Emel O. Et Al. "Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation." SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.42, pp.49-51, 2016

Akarsu, E. O. Et Al. (2016) . "Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation." SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.42, pp.49-51.

@article{article, author={Emel Oguz Akarsu Et Al. }, title={Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation}, journal={SEIZURE-EUROPEAN JOURNAL OF EPILEPSY}, year=2016, pages={49-51} }