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Page 1
Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.
Kotan LD, Ternier G, Cakir AD, Emeksiz HC, Turan I, Delpouve G, Kardelen AD, Ozcabi B, Isik E, Mengen E, Cakir EDP, Yuksel A, Agladioglu SY, Dilek SO, Evliyaoglu O, Darendeliler F, Gurbuz F, Akkus G, Yuksel B, Giacobini P, Topaloglu AK. Kotan LD, et al. Among authors: kardelen ad. Genet Med. 2021 Jun;23(6):1008-1016. doi: 10.1038/s41436-020-01087-5. Epub 2021 Jan 25. Genet Med. 2021. PMID: 33495532 Free PMC article.
A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations.
Kardelen AD, Toksoy G, Baş F, Yavaş Abalı Z, Gençay G, Poyrazoğlu Ş, Bundak R, Altunoğlu U, Avcı Ş, Najaflı A, Uyguner O, Karaman B, Başaran S, Darendeliler F. Kardelen AD, et al. J Clin Res Pediatr Endocrinol. 2018 Jul 31;10(3):206-215. doi: 10.4274/jcrpe.0032. Epub 2018 Mar 29. J Clin Res Pediatr Endocrinol. 2018. PMID: 29595516 Free PMC article.
Multi-parametric Ultrasound Evaluation of Pediatric Thyroid Dyshormonogenesis.
Adaletli I, Bayramoglu Z, Caliskan E, Yilmaz R, Akyol Sari ZN, Bas F, Kardelen AD, Poyrazoglu S, Darendeliler F. Adaletli I, et al. Among authors: kardelen ad. Ultrasound Med Biol. 2019 Jul;45(7):1644-1653. doi: 10.1016/j.ultrasmedbio.2019.03.004. Epub 2019 Apr 25. Ultrasound Med Biol. 2019. PMID: 31031038
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: kardelen ad. 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.
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. 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.
Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study.
Tarçın G, Çatlı G, Çetinkaya S, Eren E, Kardelen AD, Akıncı A, Böber E, Kara C, Yıldırım R, Er E, Polat R, Özhan B, Yıldız M, Kor Y, Evliyaoğlu O, Dündar B, Ercan O. Tarçın G, et al. Among authors: kardelen ad. Clin Endocrinol (Oxf). 2024 Jan;100(1):19-28. doi: 10.1111/cen.14980. Epub 2023 Oct 10. Clin Endocrinol (Oxf). 2024. PMID: 37814958
16 results