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Andrologia|March 1, 2019
Molecular investigation of mutations in androgen receptor and 5-alpha-reductase-2 genes in 46,XY Disorders of Sex Development with normal testicular developmentMohamadreza Ahmadifard, Abdolmohamad Kajbafzadeh, Samareh Panjeh-Shahi, et al.Journal of Diabetes and Metabolic Disorders|December 13, 2021
Placenta derived Mesenchymal Stem Cells transplantation in Type 1 diabetes: preliminary report of phase 1 clinical trialSedighegh Madani, Aria Setudeh, Hamid Reza Aghayan, et al.Orphanet Journal of Rare Diseases|January 7, 2022
Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variantsAria Setoodeh, Samareh Panjeh-Shahi, Fariba Bahmani, et al.BMC Immunology|July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel casesErta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.Journal of Child Neurology|January 16, 2018
The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry SystemMahmoud Reza Ashrafi, Zahra Rezaei, Morteza Heidari, et al.Orphanet Journal of Rare Diseases|January 8, 2025
Comprehensive Iranian guidelines for the diagnosis and management of maple syrup urine disease: an evidence- and consensus- based approachNoushin Rostampour, Setila Dalili, Hossein Moravej, et al.Pageof 3