Items where Author is "Alehabib, E."

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Darvish, H. and Azcona, L.J. and Tafakhori, A. and Mesias, R. and Ahmadifard, A. and Sanchez, E. and Habibi, A. and Alehabib, E. and Johari, A.H. and Emamalizadeh, B. and Jamali, F. and Chapi, M. and Jamshidi, J. and Kajiwara, Y. and Paisán-Ruiz, C. (2020) Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes. Scientific Reports, 10 (1).

Taghavi, S. and Chaouni, R. and Tafakhori, A. and Azcona, L.J. and Firouzabadi, S.G. and Omrani, M.D. and Jamshidi, J. and Emamalizadeh, B. and Shahidi, G.A. and Ahmadi, M. and Habibi, S.A.H. and Ahmadifard, A. and Fazeli, A. and Motallebi, M. and Petramfar, P. and Askarpour, S. and Askarpour, S. and Shahmohammadibeni, H.A. and Shahmohammadibeni, N. and Eftekhari, H. and Shafiei Zarneh, A.E. and Mohammadihosseinabad, S. and Khorrami, M. and Najmi, S. and Chitsaz, A. and Shokraeian, P. and Ehsanbakhsh, H. and Rezaeidian, J. and Ebrahimi Rad, R. and Madadi, F. and Andarva, M. and Alehabib, E. and Atakhorrami, M. and Mortazavi, S.E. and Azimzadeh, Z. and Bayat, M. and Besharati, A.M. and Harati-Ghavi, M.A. and Omidvari, S. and Dehghani-Tafti, Z. and Mohammadi, F. and Mohammad Hossein Pour, B. and Noorollahi Moghaddam, H. and Esmaili Shandiz, E. and Habibi, A. and Taherian-Esfahani, Z. and Darvish, H. and Paisán-Ruiz, C. (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.

Taghavi, S. and Chaouni, R. and Tafakhori, A. and Azcona, L.J. and Firouzabadi, S.G. and Omrani, M.D. and Jamshidi, J. and Emamalizadeh, B. and Shahidi, G.A. and Ahmadi, M. and Habibi, S.A.H. and Ahmadifard, A. and Fazeli, A. and Motallebi, M. and Petramfar, P. and Askarpour, S. and Askarpour, S. and Shahmohammadibeni, H.A. and Shahmohammadibeni, N. and Eftekhari, H. and Shafiei Zarneh, A.E. and Mohammadihosseinabad, S. and Khorrami, M. and Najmi, S. and Chitsaz, A. and Shokraeian, P. and Ehsanbakhsh, H. and Rezaeidian, J. and Ebrahimi Rad, R. and Madadi, F. and Andarva, M. and Alehabib, E. and Atakhorrami, M. and Mortazavi, S.E. and Azimzadeh, Z. and Bayat, M. and Besharati, A.M. and Harati-Ghavi, M.A. and Omidvari, S. and Dehghani-Tafti, Z. and Mohammadi, F. and Mohammad Hossein Pour, B. and Noorollahi Moghaddam, H. and Esmaili Shandiz, E. and Habibi, A. and Taherian-Esfahani, Z. and Darvish, H. and Paisán-Ruiz, C. (2018) A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations. Molecular Neurobiology.

Taghavi, S. and Chaouni, R. and Tafakhori, A. and Azcona, L.J. and Firouzabadi, S.G. and Omrani, M.D. and Jamshidi, J. and Emamalizadeh, B. and Shahidi, G.A. and Ahmadi, M. and Habibi, S.A.H. and Ahmadifard, A. and Fazeli, A. and Motallebi, M. and Petramfar, P. and Askarpour, S. and Askarpour, S. and Shahmohammadibeni, H.A. and Shahmohammadibeni, N. and Eftekhari, H. and Shafiei Zarneh, A.E. and Mohammadihosseinabad, S. and Khorrami, M. and Najmi, S. and Chitsaz, A. and Shokraeian, P. and Ehsanbakhsh, H. and Rezaeidian, J. and Ebrahimi Rad, R. and Madadi, F. and Andarva, M. and Alehabib, E. and Atakhorrami, M. and Mortazavi, S.E. and Azimzadeh, Z. and Bayat, M. and Besharati, A.M. and Harati-Ghavi, M.A. and Omidvari, S. and Dehghani-Tafti, Z. and Mohammadi, F. and Mohammad Hossein Pour, B. and Noorollahi Moghaddam, H. and Esmaili Shandiz, E. and Habibi, A. and Taherian-Esfahani, Z. and Darvish, H. and Paisán-Ruiz, C. (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.

Andarva, M. and Jamshidi, J. and Ghaedi, H. and Daftarian, N. and Emamalizadeh, B. and Alehabib, E. and Taghavi, S. and Pouriran, R. and Darvish, H. (2018) A novel c.240241insGG mutation in NDP gene in a family with Norrie disease. Clinical and Experimental Optometry.

Andarva, M. and Jamshidi, J. and Ghaedi, H. and Daftarian, N. and Emamalizadeh, B. and Alehabib, E. and Taghavi, S. and Pouriran, R. and Darvish, H. (2018) A novel c.240241insGG mutation in NDP gene in a family with Norrie disease. Clinical and Experimental Optometry, 101 (2). pp. 255-259.

Taghavi, S. and Chaouni, R. and Tafakhori, A. and Azcona, L.J. and Firouzabadi, S.G. and Omrani, M.D. and Jamshidi, J. and Emamalizadeh, B. and Shahidi, G.A. and Ahmadi, M. and Habibi, S.A.H. and Ahmadifard, A. and Fazeli, A. and Motallebi, M. and Petramfar, P. and Askarpour, S. and Askarpour, S. and Shahmohammadibeni, H.A. and Shahmohammadibeni, N. and Eftekhari, H. and Shafiei Zarneh, A.E. and Mohammadihosseinabad, S. and Khorrami, M. and Najmi, S. and Chitsaz, A. and Shokraeian, P. and Ehsanbakhsh, H. and Rezaeidian, J. and Ebrahimi Rad, R. and Madadi, F. and Andarva, M. and Alehabib, E. and Atakhorrami, M. and Mortazavi, S.E. and Azimzadeh, Z. and Bayat, M. and Besharati, A.M. and Harati-Ghavi, M.A. and Omidvari, S. and Dehghani-Tafti, Z. and Mohammadi, F. and Mohammad Hossein Pour, B. and Noorollahi Moghaddam, H. and Esmaili Shandiz, E. and Habibi, A. and Taherian-Esfahani, Z. and Darvish, H. and Paisán-Ruiz, C. (2017) A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations. Molecular Neurobiology.

Emamalizadeh, B. and Jamshidi, J. and Movafagh, A. and Ohadi, M. and khaniani, M.S. and Kazeminasab, S. and Biglarian, A. and Taghavi, S. and Motallebi, M. and Fazeli, A. and Ahmadifard, A. and Shahidi, G.-A. and Petramfar, P. and Shahmohammadibeni, N. and Dadkhah, T. and Khademi, E. and Tafakhori, A. and Khaligh, A. and Safaralizadeh, T. and Kowsari, A. and Mirabzadeh, A. and Zarneh, A.E.S. and Khorrami, M. and Shokraeian, P. and Banavandi, M.J.S. and Lima, B.S. and Andarva, M. and Alehabib, E. and Atakhorrami, M. and Darvish, H. (2017) RIT2 Polymorphisms: Is There a Differential Association? Molecular Neurobiology.

Khademi, E. and Alehabib, E. and Shandiz, E.E. and Ahmadifard, A. and Andarva, M. and Jamshidi, J. and Rahimi-Aliabadi, S. and Pouriran, R. and Nejad, F.R. and Mansoori, N. and Shahmohammadibeni, N. and Taghavi, S. and Shokraeian, P. and Akhavan-Niaki, H. and Paisán-Ruiz, C. and Darvish, H. and Ohadi, M. (2017) Support for "disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia. Genetic Testing and Molecular Biomarkers.

Andarva, M. and Jamshidi, J. and Ghaedi, H. and Daftarian, N. and Emamalizadeh, B. and Alehabib, E. and Taghavi, S. and Pouriran, R. and Darvish, H. (2017) A novel c.240241insGG mutation in NDP gene in a family with Norrie disease. Clinical and Experimental Optometry.

Jamshidi, J. and Abdollahi, S. and Ghaedi, H. and Alehabib, E. and Tafakhori, A. and Alinaghi, S. and Chapi, M. and Johari, A.H. and Darvish, H. (2017) A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome. European Journal of Medical Genetics.

Safarpour Lima, B. and Ghaedi, H. and Daftarian, N. and Ahmadieh, H. and Jamshidi, J. and Khorrami, M. and Noroozi, R. and Sohrabifar, N. and Assarzadegan, F. and Hesami, O. and Taghavi, S. and Ahmadifard, A. and Atakhorrami, M. and Rahimi-Aliabadi, S. and Shahmohammadibeni, N. and Alehabib, E. and Andarva, M. and Darvish, H. and Emamalizadeh, B. (2016) C.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European Journal of Medical Genetics, 59 (2). pp. 65-69.

Emamalizadeh, B. and Jamshidi, J. and Movafagh, A. and Ohadi, M. and Khaniani, M.S. and Kazeminasab, S. and Biglarian, A. and Taghavi, S. and Motallebi, M. and Fazeli, A. and Ahmadifard, A. and Shahidi, G.-A. and Petramfar, P. and Shahmohammadibeni, N. and Dadkhah, T. and Khademi, E. and Tafakhori, A. and Khaligh, A. and Safaralizadeh, T. and Kowsari, A. and Mirabzadeh, A. and Zarneh, A.E.S. and Khorrami, M. and Shokraeian, P. and Banavandi, M.J.S. and Lima, B.S. and Andarva, M. and Alehabib, E. and Atakhorrami, M. and Darvish, H. (2016) RIT2 Polymorphisms: Is There a Differential Association? Molecular Neurobiology. pp. 1-7.

Shahmohammadibeni, N. and Rahimi-Aliabadi, S. and Jamshidi, J. and Emamalizadeh, B. and Shahmohammadibeni, H.A. and Zare Bidoki, A. and Akhavan-Niaki, H. and Eftekhari, H. and Abdollahi, S. and Shekari Khaniani, M. and Shahmohammadibeni, M. and Fazeli, A. and Motallebi, M. and Taghavi, S. and Ahmadifard, A. and Shafiei Zarneh, A.E. and Andarva, M. and Dadkhah, T. and Khademi, E. and Alehabib, E. and Rahimi, M. and Tafakhori, A. and Atakhorrami, M. and Darvish, H. (2016) The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson�s disease in Iranian population. Neurological Sciences, 37 (5). pp. 731-736.

Rahimi-Aliabadi, S. and Daftarian, N. and Ahmadieh, H. and Emamalizadeh, B. and Jamshidi, J. and Tafakhori, A. and Ghaedi, H. and Noroozi, R. and Taghavi, S. and Ahmadifard, A. and Alehabib, E. and Andarva, M. and Shokraeian, P. and Atakhorrami, M. and Darvish, H. (2016) A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome. Eye (Basingstoke), 30 (11). pp. 1424-1432.

This list was generated on Thu Oct 29 08:47:48 2020 EDT.