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In response to: “Letter to: Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey”.
Karakılıç Özturan E, Öztürk AP, Baş F, Erdoğdu AB, Kaptan S, Kardelen Al AD, Poyrazoğlu Ş, Yıldız M, Direk N, Yüksel Ş, Darendeliler F. Karakılıç Özturan E, et al. J Clin Res Pediatr Endocrinol. 2023 Nov 22;15(4):451-452. doi: 10.4274/jcrpe.galenos.2023.2023-9-20. Epub 2023 Sep 28. J Clin Res Pediatr Endocrinol. 2023. PMID: 37752752 Free PMC article. No abstract available.
A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy.
Yavas Abali Z, Gokpinar Ili E, Bas F, Ulak Ozkan M, Gulec Ç, Toksoy G, Ozturk AP, Karakilic Ozturan E, Aslanger A, Caliskan M, Yesil G, Poyrazoglu S, Darendeliler F, Oya Uyguner Z. Yavas Abali Z, et al. Among authors: karakilic ozturan e. Horm Res Paediatr. 2024;97(2):157-164. doi: 10.1159/000532000. Epub 2023 Jul 18. Horm Res Paediatr. 2024. PMID: 37463572 Free article.
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency.
Kardelen AD, Najafli A, Baş F, Karaman B, Toksoy G, Poyrazoğlu Ş, Avcı Ş, Altunoğlu U, Yavaş Abalı Z, Öztürk AP, Karakılıç Özturan E, Başaran S, Darendeliler F, Uyguner ZO. Kardelen AD, et al. Among authors: karakilic ozturan e. J Clin Res Pediatr Endocrinol. 2023 Nov 22;15(4):338-347. doi: 10.4274/jcrpe.galenos.2023.2023-4-4. Epub 2023 Jun 20. J Clin Res Pediatr Endocrinol. 2023. PMID: 37338295 Free PMC article.
Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey.
Karakılıç Özturan E, Öztürk AP, Baş F, Erdoğdu AB, Kaptan S, Kardelen Al AD, Poyrazoğlu Ş, Yıldız M, Direk N, Yüksel Ş, Darendeliler F. Karakılıç Özturan E, et al. J Clin Res Pediatr Endocrinol. 2023 Aug 23;15(3):276-284. doi: 10.4274/jcrpe.galenos.2023.2023-1-13. Epub 2023 Mar 29. J Clin Res Pediatr Endocrinol. 2023. PMID: 36987788 Free PMC article.
SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS.
Karakilic-Ozturan E, Ozturk AP, Oney C, Kardelen Al AD, Yildirim ZY, Balci HI, Poyrazoglu S, Bas F, Darendeliler F. Karakilic-Ozturan E, et al. Acta Endocrinol (Buchar). 2022 Jul-Sep;18(3):387-391. doi: 10.4183/aeb.2022.387. Acta Endocrinol (Buchar). 2022. PMID: 36699160 Free PMC article.
A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care.
Kardelen AD, Karakılıç Özturan E, Poyrazoğlu Ş, Baş F, Ceylaner S, Joustra SD, Wit JM, Darendeliler F. Kardelen AD, et al. Among authors: karakilic ozturan e. J Clin Res Pediatr Endocrinol. 2023 Nov 22;15(4):431-437. doi: 10.4274/jcrpe.galenos.2022.2021-12-3. Epub 2022 Apr 25. J Clin Res Pediatr Endocrinol. 2023. PMID: 35466665 Free PMC article.
Evaluation of growth, puberty, osteoporosis, and the response to long-term bisphosphonate therapy in four patients with osteoporosis-pseudoglioma syndrome.
Karakilic-Ozturan E, Altunoglu U, Ozturk AP, Kardelen Al AD, Yavas Abali Z, Avci S, Wollnik B, Poyrazoglu S, Bas F, Uyguner ZO, Kayserili H, Darendeliler F. Karakilic-Ozturan E, et al. Am J Med Genet A. 2022 Jul;188(7):2061-2070. doi: 10.1002/ajmg.a.62742. Epub 2022 Apr 8. Am J Med Genet A. 2022. PMID: 35393770
Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype.
Kardelen Al AD, Gencay G, Bayramoglu Z, Aliyev B, Karakilic-Ozturan E, Poyrazoglu S, Nişli K, Bas F, Darendeliler F. Kardelen Al AD, et al. Among authors: karakilic ozturan e. Acta Endocrinol (Buchar). 2021 Apr-Jun;17(1):124-130. doi: 10.4183/aeb.2021.124. Acta Endocrinol (Buchar). 2021. PMID: 34539920 Free PMC article.
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