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Page 1
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: eroglu fk. Pediatr Nephrol. 2020 Oct;35(10):1941-1952. doi: 10.1007/s00467-020-04574-8. Epub 2020 May 11. Pediatr Nephrol. 2020. PMID: 32394188
Kidney disease profile and encountered problems during follow-up in Syrian refugee children: a multicenter retrospective study.
Balat A, Kilic BD, Aksu B, Kara MA, Buyukcelik M, Agbas A, Eroglu FK, Gungor T, Alaygut D, Yildiz N, Bastug F, Atmis B, Melek E, Elmaci M, Tulpar S, Pehlivanoglu C, Doven SS, Comak E, Tabel Y, Gemici A, Uysal B, Ozzorlar GS, Kuçuk N, Delibas A, Ozcelik G, Goknar N, Dursun I, Ertan P, Ozunan IA, Sonmez F. Balat A, et al. Among authors: eroglu fk. Pediatr Nephrol. 2022 Feb;37(2):393-402. doi: 10.1007/s00467-021-05046-3. Epub 2021 Jul 31. Pediatr Nephrol. 2022. PMID: 34331573
Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].
Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Eroglu FK, et al. Pediatr Neurol. 2019 May;94:84. doi: 10.1016/j.pediatrneurol.2018.12.017. Epub 2019 Feb 15. Pediatr Neurol. 2019. PMID: 30777605 No abstract available.
28 results