Items where Author is "Alehabib, Elham"

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Number of items: 11.

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Chapi, Marjan and Sabbaghi, Hamideh and Suri, Fatemeh and Alehabib, Elham and Rahimi-Aliabadi, Simin and Jamali, Faezeh and Jamshidi, Javad and Emamalizadeh, Babak and Darvish, Hossein and Mirrahimi, Mehraban and Ahmadieh, Hamid and Daftarian, Narsis (2019) Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. OPHTHALMIC GENETICS, 40 (3). pp. 259-266.

Taghavi, Shaghayegh and Chaouni, Rita and Tafakhori, Abbas and Azcona, Luis J and Firouzabadi, Saghar Ghasemi and Omrani, Mir Davood and Jamshidi, Javad and Emamalizadeh, Babak and Shahidi, Gholam Ali and Ahmadi, Mona and Habibi, Seyed Amir Hassan and Ahmadifard, Azadeh and Fazeli, Atena and Motallebi, Marzieh and Petramfar, Peyman and Askarpour, Saeed and Askarpour, Shiva and Shahmohammadibeni, Hossein Ali and Shahmohammadibeni, Neda and Eftekhari, Hajar and Shafiei Zarneh, Amir Ehtesham and Mohammadihosseinabad, Saeed and Khorrami, Mehdi and Najmi, Safa and Chitsaz, Ahmad and Shokraeian, Parasto and Ehsanbakhsh, Hossein and Rezaeidian, Jalal and Ebrahimi Rad, Reza and Madadi, Faranak and Andarva, Monavvar and Alehabib, Elham and Atakhorrami, Minoo and Mortazavi, Seyed Erfan and Azimzadeh, Zahra and Bayat, Mahdis and Besharati, Amir Mohammad and Harati-Ghavi, Mohammad Ali and Omidvari, Samareh and Dehghani-Tafti, Zahra and Mohammadi, Faraz and Mohammad Hossein Pour, Banafsheh and Noorollahi Moghaddam, Hamid and Esmaili Shandiz, Ehsan and Habibi, Arman and Taherian-Esfahani, Zahra and Darvish, Hossein and Paisán-Ruiz, Coro (2018) A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations. Molecular neurobiology, 55 (4). pp. 3477-3489. ISSN 1559-1182

Andarva, Monavvar and Jamshidi, Javad and Ghaedi, Hamid and Daftarian, Narsis and Emamalizadeh, Babak and Alehabib, Elham and Taghavi, Shaghyegh and Pouriran, Ramin and Darvish, Hossein (2018) A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease. Clinical & experimental optometry, 101 (2). pp. 255-259. ISSN 1444-0938

Shahmohammadibeni, Neda and Rahimi-Aliabadi, Simin and Jamshidi, Javad and Emamalizadeh, Babak and Shahmohammadibeni, Hossein Ali and Zare Bidoki, Alireza and Akhavan-Niaki, Haleh and Eftekhari, Hajar and Abdollahi, Shokoufeh and Shekari Khaniani, Mahmoud and Shahmohammadibeni, Mahnaz and Fazeli, Atena and Motallebi, Marzieh and Taghavi, Shaghayegh and Ahmadifard, Azadeh and Shafiei Zarneh, Amir Ehtesham and Andarva, Monavvar and Dadkhah, Tahereh and Khademi, Ehteram and Alehabib, Elham and Rahimi, Mahnoosh and Tafakhori, Abbas and Atakhorrami, Minoo and Darvish, Hossein (2016) The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 37 (5). pp. 731-6. ISSN 1590-3478

Emamalizadeh, Babak and Jamshidi, Javad and Movafagh, Abolfazl and Ohadi, Mina and Khaniani, Mahmoud Shekari and Kazeminasab, Somayyeh and Biglarian, Akbar and Taghavi, Shaghayegh and Motallebi, Marzieh and Fazeli, Atena and Ahmadifard, Azadeh and Shahidi, Gholam-Ali and Petramfar, Peyman and Shahmohammadibeni, Neda and Dadkhah, Tahereh and Khademi, Ehteram and Tafakhori, Abbas and Khaligh, Ali and Safaralizadeh, Tannaz and Kowsari, Ali and Mirabzadeh, Arash and Zarneh, Amir Ehtesham Shafiei and Khorrami, Mehdi and Shokraeian, Parasto and Banavandi, Mohammad Javad Soltani and Lima, Behnam Safarpour and Andarva, Monavvar and Alehabib, Elham and Atakhorrami, Minoo and Darvish, Hossein (2016) RIT2 Polymorphisms: Is There a Differential Association? Molecular neurobiology. ISSN 1559-1182

Safarpour Lima, Behnam and Ghaedi, Hamid and Daftarian, Narsis and Ahmadieh, Hamid and Jamshidi, Javad and Khorrami, Mehdi and Noroozi, Rezvan and Sohrabifar, Nasim and Assarzadegan, Farhad and Hesami, Omid and Taghavi, Shaghayegh and Ahmadifard, Azadeh and Atakhorrami, Minoo and Rahimi-Aliabadi, Simin and Shahmohammadibeni, Neda and Alehabib, Elham and Andarva, Monavvar and Darvish, Hossein and Emamalizadeh, Babak (2016) c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European journal of medical genetics, 59 (2). pp. 65-9. ISSN 1878-0849

Alehabib, Elham and Jamshidi, Javad and Ghaedi, Hamid and Askarian, Fahimeh and Mahmoudieh, Leila and Johari, Amir Hossein and Darvish, Hossein Bioinformatic Tools To Determine The Pathogenicity Of A Missense Mutation In Pkhd1 In Autosomal Recessive Polycystic Kidney Disease. NEPHROLOGY, 22 (4). pp. 330-331.

Taghavi, Shaghayegh and Chaouni, Rita and Tafakhori, Abbas and Azcona, Luis J. and Firouzabadi, Saghar Ghasemi and Omrani, Mir Davood and Jamshidi, Javad and Emamalizadeh, Babak and Shahidi, Gholam Ali and Ahmadi, Mona and Habibi, Seyed Amir Hassan and Ahmadifard, Azadeh and Fazeli, Atena and Motallebi, Marzieh and Petramfar, Peyman and Askarpour, Saeed and Askarpour, Shiva and Shahmohammadibeni, Hossein Ali and Shahmohammadibeni, Neda and Eftekhari, Hajar and Zarneh, Amir Ehtesham Shafiei and Mohammadihosseinabad, Saeed and Khorrami, Mehdi and Najmi, Safa and Chitsaz, Ahmad and Shokraeian, Parasto and Ehsanbakhsh, Hossein and Rezaeidian, Jalal and Rad, Reza Ebrahimi and Madadi, Faranak and Andarva, Monavvar and Alehabib, Elham and Atakhorrami, Minoo and Mortazavi, Seyed Erfan and Azimzadeh, Zahra and Bayat, Mahdis and Besharati, Amir Mohammad and Harati-Ghavi, Mohammad Ali and Omidvari, Samareh and Dehghani-Tafti, Zahra and Mohammadi, Faraz and Pour, Banafsheh Mohammad Hossein and Moghaddam, Hamid Noorollahi and Shandiz, Ehsan Esmaili and Habibi, Arman and Taherian-Esfahani, Zahra and Darvish, Hossein and Paisan-Ruiz, Coro A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations. MOLECULAR NEUROBIOLOGY, 55 (4). pp. 3477-3489.

Alehabib, Elham and Jamshidi, Javad and Ghaedi, Hamid and Emamalizadeh, Babak and Andarva, Monavvar and Daftarian, Narsis and Kanavi, Mozhgan Rezaei and Torbati, Peyman Mohammadi and Espandar, Goldis and Alinaghi, Somayeh and Johari, Amir Hossein and Saghally, Mansoor and Mohajerani, Fatemeh and Darvish, Hossein Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD). INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE, 6 (4). pp. 204-211.

Emamalizadeh, Babak and Jamshidi, Javad and Movafagh, Abolfazl and Ohadi, Mina and Khaniani, Mahmoud Shekari and Kazeminasab, Somayyeh and Biglarian, Akbar and Taghavi, Shaghayegh and Motallebi, Marzieh and Fazeli, Atena and Ahmadifard, Azadeh and Shahidi, Gholam-Ali and Petramfar, Peyman and Shahmohammadibeni, Neda and Dadkhah, Tahereh and Khademi, Ehteram and Tafakhori, Abbas and Khaligh, Ali and Safaralizadeh, Tannaz and Kowsari, Ali and Mirabzadeh, Arash and Zarneh, Amir Ehtesham Shafiei and Khorrami, Mehdi and Shokraeian, Parasto and Banavandi, Mohammad Javad Soltani and Lima, Behnam Safarpour and Andarva, Monavvar and Alehabib, Elham and Atakhorrami, Minoo and Darvish, Hossein RIT2 Polymorphisms: Is There a Differential Association? MOLECULAR NEUROBIOLOGY, 54 (3). pp. 2234-2240.

Andarva, Monavvar and Jamshidi, Javad and Ghaedi, Hamid and Daftarian, Narsis and Emamalizadeh, Babak and Alehabib, Elham and Taghavi, Shaghyegh and Pouriran, Ramin and Darvish, Hossein A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease. CLINICAL AND EXPERIMENTAL OPTOMETRY, 101 (2). pp. 255-259.

This list was generated on Tue Oct 20 04:14:44 2020 EDT.