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BMC Public Health|April 18, 2021
Gender difference in determinant factors of being overweight among the 40-70-year-old population of Kharameh cohort study, IranSeyed Alireza Dastgheib, Abbas Rezaianzadeh, Najmeh Maharlouei, et al.Journal of Diabetes and Metabolic Disorders|December 13, 2021
Association of ACE I/D and PAI-1 4G/5G polymorphisms with susceptibility to type 2 diabetes mellitusSomaye Miri, Mohammad Hasan Sheikhha, Seyed Alireza Dastgheib, et al.Arquivos De Gastroenterologia|April 16, 2020
ASSOCIATION OF IL-8 -251T>A (RS4073) POLYMORPHISM WITH SUSCEPTIBILITY TO GASTRIC CANCER: A SYSTEMATIC REVIEW AND META-ANALYSIS BASED ON 33 CASE-CONTROL STUDIESMansour Moghimi, Seyed Alireza Dastgheib, Naeimeh Heiranizadeh, et al.European Journal of Medical Genetics|October 4, 2021
A novel non-sense mutation in TDP2 causes spinocerebellar ataxia autosomal recessive 23 accompanied by bilateral upward gaze; report of a case and review of the literatureSina Zoghi, Hossein Jafari Khamirani, Hamidreza Hassanipour, et al.Journal of Medical Case Reports|January 4, 2026
A novel pathogenic mutation in TSPEAR associated with sensorineural hearing loss: a case report and review of the literatureAlireza Ahmadkhani, Erfan Taherifard, Sina Zoghi, et al.Journal of Orthopaedic Surgery and Research|June 10, 2024
A thorough analysis of data on the correlation between COL9A1 polymorphisms and the susceptibility to congenital talipes equinovarus: a meta-analysisMohammad Golshan-Tafti, Seyed Alireza Dastgheib, Kamran Alijanpour, et al.Frontiers in Endocrinology|November 12, 2016
A Candidate Gene Association Study of Bone Mineral Density in an Iranian PopulationSeyed Alireza Dastgheib, Alison Gartland, Seyed Mohammad Bagher Tabei, et al.Revista Brasileira De Ortopedia|March 4, 2020
Association of the IL-6 -174G > C (rs1800795) Polymorphism with Adolescent Idiopathic Scoliosis: Evidence from a Case-Control Study and Meta-AnalysisMohammad Reza Sobhan, Masoud Mahdinezhad-Yazdi, Seyed Alireza Dastgheib, et al.Iranian Journal of Public Health|September 10, 2019
Association of MMP-2-753C>T and MMP-9-1562C>T Polymorphisms with Chronic/Aggressive Periodontitis Risk: A Systematic Review and Meta-AnalysisFatemeh Mashhadiabbas, Hossein Neamatzadeh, Elnaz Foroughi, et al.Human Genome Variation|January 12, 2023
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature reviewZahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, et al.Pageof 11