MEG3 lncRNA is over-expressed in autism spectrum disorder von Taheri, Mohammad, Honarmand Tamizkar, Kasra, Omrani, Shaghayegh, Arsang-Jang, Shahram, Ghafouri-Fard, Soudeh, Omrani, Mir Davood

Volltext

The effect of omega-3 fatty acids on clinical and paraclinical features of intractable epileptic patients: a triple blind randomized clinical trial von Omrani, Shaghayegh, Taheri, Mohammad, Omrani, Mir Davood, Arsang-Jang, Shahram, Ghafouri-Fard, Soudeh

Volltext

Comparing the Effects of Topical Miltefosine and Glucantime in Treatment of Cutaneous Leishmaniasis von Ali Asilian, Shaghayegh Omrani, Mohammad Ail Nilforoushzadeh

Volltext

HOTAIR genetic variants are associated with prostate cancer and benign prostate hyperplasia in an Iranian population von Taheri, Mohammad, Habibi, Mohsen, Noroozi, Rezvan, Rakhshan, Azadeh, Sarrafzadeh, Shaghayegh, Sayad, Arezou, Omrani, Mir Davood, Ghafouri-Fard, Soudeh

Volltext

Association of ANRIL gene polymorphisms with prostate cancer and benign prostatic hyperplasia in an Iranian population von Taheri, Mohammad, Pouresmaeili, Farkhondeh, Omrani, Mir Davood, Habibi, Mohsen, Sarrafzadeh, Shaghayegh, Noroozi, Rezvan, Rakhshan, Azadeh, Sayad, Arezou, Ghafouri-Fard, Soudeh

Volltext

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

Volltext

A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations von Taghavi, Shaghayegh, Chaouni, Rita, Tafakhori, Abbas, Azcona, Luis J., Firouzabadi, Saghar Ghasemi, Omrani, Mir Davood, Jamshidi, Javad, Emamalizadeh, Babak, Shahidi, Gholam Ali, Ahmadi, Mona, Habibi, Seyed Amir Hassan, Ahmadifard, Azadeh, Fazeli, Atena, Motallebi, Marzieh, Petramfar, Peyman, Askarpour, Saeed, Askarpour, Shiva, Shahmohammadibeni, Hossein Ali, Shahmohammadibeni, Neda, Eftekhari, Hajar, Shafiei Zarneh, Amir Ehtesham, Mohammadihosseinabad, Saeed, Khorrami, Mehdi, Najmi, Safa, Chitsaz, Ahmad, Shokraeian, Parasto, Ehsanbakhsh, Hossein, Rezaeidian, Jalal, Ebrahimi Rad, Reza, Madadi, Faranak, Andarva, Monavvar, Alehabib, Elham, Atakhorrami, Minoo, Mortazavi, Seyed Erfan, Azimzadeh, Zahra, Bayat, Mahdis, Besharati, Amir Mohammad, Harati-Ghavi, Mohammad Ali, Omidvari, Samareh, Dehghani-Tafti, Zahra, Mohammadi, Faraz, Mohammad Hossein Pour, Banafsheh, Noorollahi Moghaddam, Hamid, Esmaili Shandiz, Ehsan, Habibi, Arman, Taherian-Esfahani, Zahra, Darvish, Hossein, Paisán-Ruiz, Coro

Volltext

Synaptosome-Associated Protein 25 (SNAP25) Gene Association Analysis Revealed Risk Variants for ASD, in Iranian Population von Safari, Mohammad reza, Omrani, Mir Davood, Noroozi, Rezvan, Sayad, Arezou, Sarrafzadeh, Shaghayegh, Komaki, Alireza, Manjili, Fateme Asadzadeh, Mazdeh, Mehrdokht, Ghaleiha, Ali, Taheri, Mohammad

Volltext

PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism: PTRHD1 Mutation In ID and Parkinsonism von 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

Volltext

Phospholipase D1 expression analysis in relapsing-remitting multiple sclerosis patients von Eftekharian, Mohammad Mahdi, Azimi, Tahereh, Ghafouri-Fard, Soudeh, Sayad, Arezou, Omrani, Mir Davood, Sarrafzadeh, Shaghayegh, Abbasalipourkabir, Roghayeh, Mazdeh, Mehrdokht, Taheri, Mohammad

Volltext

Association of von Taheri, Mohammad, Pouresmaeili, Farkhondeh, Omrani, Mir Davood, Habibi, Mohsen, Sarrafzadeh, Shaghayegh, Noroozi, Rezvan, Rakhshan, Azadeh, Sayad, Arezou, Ghafouri-Fard, Soudeh

Volltext