Items where Author is "Azcona, L.J."

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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.

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.

This list was generated on Thu Oct 29 10:20:23 2020 EDT.