Items where Author is "Petramfar, P."

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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.

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.

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.

Jamshidi, J. and Movafagh, A. and Emamalizadeh, B. and Zare Bidoki, A. and Manafi, A. and Ghasemi Firouzabadi, S. and Shahidi, G.-A. and Kazeminasab, S. and Petramfar, P. and Fazeli, A. and Motallebi, M. and Mortazavi-Tabatabaei, S.A. and Kowsari, A. and Jafarian, Z. and Darvish, H. (2014) HLA-DRA is associated with Parkinson's disease in Iranian population. International Journal of Immunogenetics, 41 (6). pp. 508-511.

This list was generated on Sun Mar 7 05:53:24 2021 EST.