1. Dominant LMAN2L mutation causes intellectual disability with remitting epilepsy. Issue 4 (7th March 2019) Authors: Alkhater, Reem A.; Wang, Peixiang; Ruggieri, Alessandra; Israelian, Lori; Walker, Susan; Scherer, Stephen W.; Smith, Mary Lou; Minassian, Berge A. Journal: Annals of clinical and translational neurology Issue: Volume 6:Issue 4(2019) Page Start: 807 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype. (June 2017) Authors: Dad, Rubina; Walker, Susan; Scherer, Stephen W.; Hassan, Muhammad Jawad; Alghamdi, Mohammad Domaia; Minassian, Berge A.; Alkhater, Reem A. Journal: Neurology Issue: Volume 3:Number 3(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. PI4K2A deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndrome. Issue 12 (24th October 2018) Authors: Alkhater, Reem A.; Scherer, Stephen W.; Minassian, Berge A.; Walker, Susan Journal: Annals of clinical and translational neurology Issue: Volume 5:Issue 12(2018) Page Start: 1617 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder – deafness syndrome. Issue 1 (24th November 2020) Authors: Alkhater, Reem A.; Ahonen, Saija; Minassian, Berge A. Journal: Annals of clinical and translational neurology Issue: Volume 8:Issue 1(2021) Page Start: 252 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗