Tehran University of Medical Sciences (TUMS) / دانشگاه علوم پزشکی تهران

Statin and nodal knee osteoarthritis: a longitudinal propensity score-matched study on the knee osteoarthritis from the osteoarthritis initiative (OAI) cohort (2019) Haj-Mirzaian A, Mohajer B, Guermazi A, Roemer F, Lima J, Blaha MJ, Bingham CO, Demehri S Conference contribution Association of patella alta with worsening of patellofemoral osteoarthritis-related structural damage: data from the Osteoarthritis Initiative (2019) Haj-Mirzaian A, Guermazi A, Pishgar F, Pourvaziri A, Roemer F, Sereni C, Hakky M, et al. Journal article Patellofemoral morphology measurements and their associations with tibiofemoral osteoarthritis-related structural damage: exploratory analysis on the osteoarthritis initiative (2019) Haj-Mirzaian A, Guermazi A, Pishgar F, Roemer F, Sereni C, Hakky M, Zikria B, Demehri S Journal article Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out” (2019) Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al. Journal article Heberden's Nodes and Knee Osteoarthritis–Related Osseous Structural Damage: Exploratory Study From the Osteoarthritis Initiative (2019) Haj-Mirzaian A, Mohajer B, Guermazi A, Shakoor D, Haugen IK, Roemer F, Demehri S Journal article Association of plasma PCB levels and HbA1c concentration in Iran (2018) Eftekhari S, Aminian O, Moinfar Z, Schettgen T, Kaifie A, Felten M, Kraus T, Esser A Journal article A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity (2018) Beziat V, Li J, Lin JX, Ma CS, Li P, Bousfiha A, Pellier I, et al. Journal article The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to beta-papillomaviruses (2018) De Jong SJ, Crequer A, Matos I, Hum D, Gunasekharan V, Lorenzo L, Jabot-Hanin F, et al. Journal article The p.Arg435His Variation of IgG3 With High Affinity to FcRn Is Associated With Susceptibility for Pemphigus Vulgaris-Analysis of Four Different Ethnic Cohorts (2018) Recke A, Konitzer S, Lemcke S, Freitag M, Sommer NM, Abdelhady M, Amoli MM, et al. Journal article Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017) Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al. Journal article