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Pteridine and tryptophan pathways in children with type 1 diabetes: Isoxanthopterin as an indicator of endothelial dysfunction.
Özer Y, Cansever MŞ, Turan H, Bayramoğlu E, Bingöl Aydın D, İşat E, Ceyhun E, Zubarioğlu T, Aktuğlu Zeybek AÇ, Kıykım E, Evliyaoğlu O. Özer Y, et al. Among authors: evliyaoglu o. J Pharm Biomed Anal. 2024 Jun 15;243:116072. doi: 10.1016/j.jpba.2024.116072. Epub 2024 Feb 27. J Pharm Biomed Anal. 2024. PMID: 38437786
Proteinuria in a patient with Graves' disease: Questions.
Dagdeviren Cakir A, Canpolat N, Saygili S, Kilicaslan I, Turan H, Ercan O, Evliyaoglu O. Dagdeviren Cakir A, et al. Among authors: evliyaoglu o. Pediatr Nephrol. 2019 Aug;34(8):1379-1381. doi: 10.1007/s00467-019-04220-y. Epub 2019 Mar 6. Pediatr Nephrol. 2019. PMID: 30843109 No abstract available.
Proteinuria in a patient with Graves' disease: Answers.
Dagdeviren Cakir A, Canpolat N, Saygili S, Kilicaslan I, Turan H, Ercan O, Evliyaoglu O. Dagdeviren Cakir A, et al. Among authors: evliyaoglu o. Pediatr Nephrol. 2019 Aug;34(8):1383-1385. doi: 10.1007/s00467-019-04221-x. Epub 2019 Mar 6. Pediatr Nephrol. 2019. PMID: 30843111 No abstract available.
An Unusual Presentation of Carney Complex.
Dağdeviren Çakır A, Turan H, Celkan T, Çomunoğlu N, Ercan O, Evliyaoğlu O. Dağdeviren Çakır A, et al. Among authors: evliyaoglu o. J Clin Res Pediatr Endocrinol. 2020 Mar 19;12(1):117-121. doi: 10.4274/jcrpe.galenos.2019.2019.0043. Epub 2019 May 23. J Clin Res Pediatr Endocrinol. 2020. PMID: 31117334 Free PMC article.
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome.
Dağdeviren Çakır A, Baş F, Akın O, Şıklar Z, Özcabı B, Berberoğlu M, Kardelen AD, Bayramoğlu E, Poyrazoğlu Ş, Aydın M, Törel Ergür A, Gökşen D, Bolu S, Aycan Z, Tüysüz B, Ercan O, Evliyaoğlu O. Dağdeviren Çakır A, et al. Among authors: evliyaoglu o. J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):308-319. doi: 10.4274/jcrpe.galenos.2021.2020.0228. Epub 2021 Feb 10. J Clin Res Pediatr Endocrinol. 2021. PMID: 33565750 Free PMC article.
Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy.
Tarcin G, Turan H, Dagdeviren Cakir A, Ozer Y, Aykut A, Alpman Durmaz A, Ercan O, Evliyaoglu O. Tarcin G, et al. Among authors: evliyaoglu o. J Pediatr Endocrinol Metab. 2021 Apr 21;34(8):1049-1053. doi: 10.1515/jpem-2020-0699. Print 2021 Aug 26. J Pediatr Endocrinol Metab. 2021. PMID: 33882198
192 results