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

door Adibi, Peyman, Akbari, Leila, Kahangi, Leila Sadat, Abdi, Fatemeh
Gepubliceerd in 2012

New pathogenic variations of mitochondrial DNA in Alzheimer disease!!

door Nia, Samira Sheibani, Azadfar, Parisa, Akbari, Leila, Assarzadegan, Farhad, Kamalidehghan, Behnam, Maroof, Hamid Reza, Houshmand, Massoud
Gepubliceerd in 2013

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

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

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

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

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

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

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

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