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Page 1
The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome.
Özdemir G, Gülhan B, Kurt-Şükür ED, Atayar E, Atan R, Dursun İ, Özçakar ZB, Saygılı S, Soylu A, Söylemezoğlu O, Yılmaz A, Bayazıt AK, Kara Eroğlu F, Kasap Demir B, Yüksel S, Tabel Y, Ağbaş A, Düzova A, Hayran M, Özaltın F, Topaloğlu R. Özdemir G, et al. Among authors: atayar e. Turk J Pediatr. 2023;65(3):456-468. doi: 10.24953/turkjped.2022.735. Turk J Pediatr. 2023. PMID: 37395965 Free article.
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
Ozdemir G, Gulhan B, Atayar E, Saygılı S, Soylemezoglu O, Ozcakar ZB, Eroglu FK, Candan C, Demir BK, Soylu A, Yüksel S, Alpay H, Agbas A, Duzova A, Hayran M, Ozaltin F, Topaloglu R. Ozdemir G, et al. Among authors: atayar e. Pediatr Nephrol. 2020 Oct;35(10):1941-1952. doi: 10.1007/s00467-020-04574-8. Epub 2020 May 11. Pediatr Nephrol. 2020. PMID: 32394188
The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study.
Tutal O, Gulhan B, Atayar E, Yuksel S, Ozcakar ZB, Soylemezoglu O, Saygili S, Caliskan S, Inozu M, Baskin E, Duzova A, Hayran M, Topaloglu R, Ozaltin F. Tutal O, et al. Among authors: atayar e. Nephron. 2024;148(5):319-332. doi: 10.1159/000528258. Epub 2023 Jan 19. Nephron. 2024. PMID: 36657418
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.
Canpolat N, Liu D, Atayar E, Saygili S, Kara NS, Westfall TA, Ding Q, Brown BJ, Braun TA, Slusarski D, Karli Oguz K, Ozluk Y, Tuysuz B, Tastemel Ozturk T, Sever L, Sezerman OU, Topaloglu R, Caliskan S, Attanasio M, Ozaltin F. Canpolat N, et al. Among authors: atayar e. Clin Genet. 2022 Mar;101(3):346-358. doi: 10.1111/cge.14105. Epub 2022 Jan 7. Clin Genet. 2022. PMID: 34964109 Free PMC article.