Health-State Utilities in Liver Cirrhosis: A Cross-sectional Study

par Adibi, Peyman, Akbari, Leila, Kahangi, Leila Sadat, Abdi, Fatemeh
Publié 2012

New pathogenic variations of mitochondrial DNA in Alzheimer disease!!

par Nia, Samira Sheibani, Azadfar, Parisa, Akbari, Leila, Assarzadegan, Farhad, Kamalidehghan, Behnam, Maroof, Hamid Reza, Houshmand, Massoud
Publié 2013

Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicities

par Allahdini, Mojgan, Kamalidehghan, Behnam, Akbari, Leila, Azadfar, Parisa, Rahmani, Ali, Ahmadipour, Fatemeh, Meng, Goh Yong, Masserrat, Abbas, Houshmand, Massoud
Publié dans Drug Des Devel Ther (2015)

Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C

par Maserrat, Shahin, Sharifpanah, Fatemeh, Akbari, Leila, Tonekaboni, Seyed Hasan, Karimzadeh, Parvaneh, Asharafi, Mahmood Reza, Mazrouei, Safoura, Sauer, Heinrich, Houshmand, Massoud
Publié dans Biomed Rep (2018)

Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C

par Maserrat, Shahin, Sharifpanah, Fatemeh, Akbari, Leila, Tonekaboni, Seyed Hasan, Karimzadeh, Parvaneh, Asharafi, Mahmood Reza, Mazrouei, Safoura, Sauer, Heinrich, Houshmand, Massoud
Publié dans Biomed Rep (2018)

Prevalence of the CYP2D6*10 (C100T), *4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicities

par Bagheri, Ali, Kamalidehghan, Behnam, Haghshenas, Maryam, Azadfar, Parisa, Akbari, Leila, Sangtarash, Mohammad Hossein, Vejdandoust, Faramarz, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Publié dans Drug Des Devel Ther (2015)