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Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
Vaseghi P, Habibi L, Neidich JA, Cao Y, Fattahi N, Rashidi-Nezhad R, Salehnezhad T, Dalili H, Rahimi Sharbaf F, Zarkesh MR, Malekian M, Mokhberdezfuli M, Mehrtash A, Ardeshirdavani A, Kariminejad R, Ghorbansabagh V, Sadeghimoghadam P, Naddaf A, Esmaeilnia Shirvany T, Mosayebi Z, Sahebdel B, Golshahi F, Shirazi M, Shamel S, Moeini R, Heidari A, Daneshmand MA, Ghasemi R, Akrami SM, Rashidi-Nezhad A. Vaseghi P, et al. Among authors: ghasemi r. Eur J Hum Genet. 2024 Jan 26. doi: 10.1038/s41431-024-01533-x. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38278869
Combined use of hair follicle stem cells and CEPO (carbamylated erythropoietin)-Fc in a rat model of chronic cerebral hypoperfusion: A behavioral, electrophysiological, and molecular study.
Hooshmandi E, Akbari S, Pandamooz S, Ghobadi M, Ghasemi R, Maghsoudi N, Rai SN, Borhani-Haghighi A, Salehi MS, Azarpira N, YousefiNejad A, Haghani M, Bayat M. Hooshmandi E, et al. Among authors: ghasemi r. Behav Brain Res. 2023 Oct 2;454:114655. doi: 10.1016/j.bbr.2023.114655. Epub 2023 Sep 4. Behav Brain Res. 2023. PMID: 37666305
149 results