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Page 1
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2.
Turan H, Dağdeviren Çakır A, Özer Y, Tarçın G, Özcabi B, Ceylaner S, Ercan O, Evliyaoğlu SO. Turan H, et al. Among authors: dagdeviren cakir a. J Clin Res Pediatr Endocrinol. 2021 Jun 2;13(2):232-238. doi: 10.4274/jcrpe.galenos.2020.2019.0216. Epub 2020 Jun 16. J Clin Res Pediatr Endocrinol. 2021. PMID: 32539318 Free PMC article.
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. 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. 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. 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. 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: dagdeviren cakir a. 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
Elevated Urinary VEGF-A, Transferrin, and Angiotensinogen Levels in Normoalbuminuric Children and Adolescents with Type 1 Diabetes: Can They Be Early Markers of Diabetic Kidney Disease?
Dağdeviren Çakır A, Saygılı SK, Canpolat N, Konukoğlu D, Turan H, Çalışkan S, Sever L, Ercan O, Evliyaoğlu O. Dağdeviren Çakır A, et al. Horm Res Paediatr. 2021;94(11-12):426-432. doi: 10.1159/000521447. Epub 2021 Dec 14. Horm Res Paediatr. 2021. PMID: 34915504
17 results