Epileptic syndromes: From clinic to genetic

Por Tafakhori, Abbas, Aghamollaii, Vajiheh, Faghihi-Kashani, Sara, Sarraf, Payam, Habibi, Laleh
Publicado no Iran J Neurol (2015)

Paget's disease of bone presented as normal pressure hydrocephalus: A case report and review of literature

Por Tafakhori, Abbas, Sadaghiani, Mohammad Salehi, Harirchian, Mohammad Hossein, Taheri, Zeinab, Aghamollaii, Vajiheh
Publicado em 2012

Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage

Por Pishnamazi, Morteza, Tafakhori, Abbas, Loloee, Sogol, Modabbernia, Amirhossein, Aghamollaii, Vajiheh, Bahrami, Bahador, Winston, Joel S.
Publicado no Cortex (2016)

From a simple chronic headache to neurobrucellosis: a case report

Por Tajdini, Masih, Akbarloo, Sona, Hosseini, Seyed MohammadReza, Parvizi, Banafsheh, Baghani, Somaye, Aghamollaii, Vajiheh, Tafakhori, Abbas
Publicado em 2014

Evaluation of partial epilepsy in Iran: role of video-EEG, EEG, and MRI with epilepsy protocol

Por Tafakhori, Abbas, Aghamollaii, Vajiheh, Modabbernia, Amir Hossein, Ghaffarpour, Majid, Omrani, Hossein Ali Ghelichnia, Harirchian, Mohammad Hossein, Mousavi, Mahsa, Faraji, Parastoo
Publicado em 2011

PTRHD1 (C2orf79) mutations lead to autosomal recessive intellectual disability and parkinsonism

Por Khodadadi, Hamidreza, Azcona, Luis J., Aghamollaii, Vajiheh, Omrani, Mir Davood, Garshasbi, Masoud, Taghavi, Shaghayegh, Tafakhori, Abbas, Shahidi, Gholam Ali, Jamshidi, Javad, Darvish, Hossein, Paisán-Ruiz, Coro
Publicado no Mov Disord (2016)