Search Results - Mohammad Shariati
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Exploring undergraduate medical students’ perception of learning procedural skills and its outcomes in clinical settings by MOHAMMAD REZA MANSOORIAN, MOHAMMAD JALILI, SHAHLA KHOSRAVAN, MOHAMMAD SHARIATI
Published in Journal of Advances in Medical Education and Professionalism (2019-10-01)Get full text
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Economic Inequality in Eye Care Utilization and its Determinants: A Blinder–Oaxaca Decomposition by Mohammad Hassan Emamian, Hojjat Zeraati, Reza Majdzadeh, Mohammad Shariati, Hassan Hashemi, Akbar Fotouhi
Published in International Journal of Health Policy and Management (2014-11-01)Get full text
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Measuring Customers’ Perception At MOHME Department Of Health, With National Productivity And Organizational Excellence Award Of Iran by Seyed Davood Nasrollapour Shirvani, Mohammad Esmaeil Motlagh, Mohammad Shariati, Pari Haji Seiyed Azizi, Azin Nahvijou
Published in پیاورد سلامت (2016-03-01)Get full text
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The effect of online education of men’s reproductive health before childbearing on knowledge, attitudes, and behaviors of preconception health in couples: A randomized controlled t... by Zahra Motaghi, Mohammad Shariati, Rahim Tahmasebi, Solmaz Mohammadi, Sherafat Akaberian, Fatemeh Malchi, Rashin Palizban, Zeinab Rabiei
Published in Journal of Education and Health Promotion (2025-05-01)Get full text
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Calpain 7 as a novel candidate gene in genetic generalized epilepsy by Faezeh Jamali, Mohammad Shariati, Mohammadtagi Farzadfard, Juliane Winkelmann, Mohsen Foroughipour, Mir Salar Kahaei, Ariane Sadr-Nabavi, Michael Zech
Published in Iranian Journal of Basic Medical Sciences (2025-10-01)Get full text
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The prevalence of SMN gene deletion/duplication in spinal muscular atrophy families referred to neuro-genetic centers of Mashhad, Iran by Mohammad Shariati, Alireza Davoudi, Reza Boostani, Farah Ashrafzadeh, Mehran Beiraghi Toosi, Nafiseh Todarbary, Javad Akhondian, Narges Hashemi, Ariane Sadr-Nabavi
Published in Egyptian Journal of Medical Human Genetics (2024-07-01)Get full text
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Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease by Mohammad Reza Seyedtaghia, Mohammad Soudyab, Mohammad Shariati, Reza Jafarzadeh Esfehani, Shabnam Vafadar, Neda Shalaei, Vahid Nouri, Michael Zech, Julianne Winkelmann, Ali shoeibi, Ariane Sadr-Nabavi
Published in Heliyon (2023-04-01)Get full text
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