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Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
Shirzadeh T, Saeidian AH, Bagherian H, Salehpour S, Setoodeh A, Alaei MR, Youssefian L, Samavat A, Touati A, Fallah MS, Vahidnezhad H, Karimipoor M, Azadmehr S, Raeisi M, Bandehi Sarhadi A, Zafarghandi Motlagh F, Jamali M, Zeinali Z, Abiri M, Zeinali S; Additional individual contributors. Shirzadeh T, et al. Among authors: azadmehr s. J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29. J Inherit Metab Dis. 2018. PMID: 30159852
GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
Zeinali S, Davoudi-Dehaghani E, Azadmehr S, DabbaghBagheri S, Bagherian H, Jamali M, Zafarghandimotlagh F, Masoodifard M, BandehiSarhaddi A, Rejali L, Sahebi S. Zeinali S, et al. Among authors: azadmehr s. Eur Arch Otorhinolaryngol. 2015 Sep;272(9):2255-9. doi: 10.1007/s00405-014-3171-7. Epub 2014 Jul 11. Eur Arch Otorhinolaryngol. 2015. PMID: 25012701
The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.
Azadmehr S, Rahiminejad F, Zafarghandi Motlagh F, Jamali M, Ghazizadeh Tehrani P, Shirzadeh T, Bagherian H, Karimipoor M, Davoudi-Dehaghani E, Zeinali S. Azadmehr S, et al. Arch Iran Med. 2021 Dec 1;24(12):887-896. doi: 10.34172/aim.2021.133. Arch Iran Med. 2021. PMID: 35014236 Free article.