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Page 1
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: ercan 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: ercan 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: ercan 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 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: ercan o. 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.
159 results