A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population

por Maryami, Fereshteh, Azarkeivan, Azita, Fallah, Mohammad Sadegh, Zeinali, Sirous
Publicado 2015

The Projection of Burden of Disease in Islamic Republic of Iran to 2025

por Khajehkazemi, Razieh, Sadeghirad, Behnam, Karamouzian, Mohammad, Fallah, Mohammad-Sadegh, Mehrolhassani, Mohammad-Hossien, Dehnavieh, Reza, Haghdoost, AliAkbar
Publicado 2013

ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants

por Dehnavi, Ali Zare, Heidari, Erfan, Rasulinezhad, Maryam, Heidari, Morteza, Ashrafi, Mahmoud Reza, Hosseini, Mohammad Mahdi, Sadeghzadeh, Fatemeh, Fallah, Mohammad-Sadegh, Rostampour, Noushin, Bahraini, Amir, Garshasbi, Masoud, Tavasoli, Ali Reza
Publicado 2021

Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS)

por Daneshpour, Maryam S, Fallah, Mohammad-Sadegh, Sedaghati-Khayat, Bahareh, Guity, Kamran, Khalili, Davood, Hedayati, Mehdi, Ebrahimi, Ahmad, Hajsheikholeslami, Farhad, Mirmiran, Parvin, Ramezani Tehrani, Fahimeh, Momenan, Amir-Abbas, Ghanbarian, Arash, Amouzegar, Atieh, Amiri, Parisa, Azizi, Fereidoun
Publicado 2017

Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta

por Tran, Thao T., Keller, Rachel B., Guillemyn, Brecht, Pepin, Melanie, Corteville, Jane E., Khatib, Samir, Fallah, Mohammad-Sadegh, Zeinali, Sirous, Malfait, Fransiska, Symoens, Sofie, Coucke, Paul, Witters, Peter, Levtchenko, Elena, Bagherian, Hamideh, Nickerson, Deborah A., Bamshad, Michael J., Chong, Jessica X., Byers, Peter H.
Publicado 2021