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Page 1
Did you mean mengel e[Author] (143 results)?
Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
Özsu E, Çetinkaya S, Bolu S, Hatipoğlu N, Savaş Erdeve Ş, Evliyaoğlu O, Baş F, Çayır A, Dündar İ, Akbaş ED, Uçaktürk SA, Berberoğlu M, Şıklar Z, Özalkak Ş, Muratoğlu Şahin N, Keskin M, Şiraz ÜG, Turan H, Öztürk AP, Mengen E, Sağsak E, Dursun F, Akyürek N, Odabaşı Güneş S, Aycan Z. Özsu E, et al. Among authors: mengen e. J Clin Res Pediatr Endocrinol. 2024 Sep 5;16(3):297-305. doi: 10.4274/jcrpe.galenos.2024.2023-10-16. Epub 2024 Apr 26. J Clin Res Pediatr Endocrinol. 2024. PMID: 38665000 Free PMC article.
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.
Siklar Z, Camtosun E, Bolu S, Yildiz M, Akinci A, Bas F, Dündar İ, Bestas A, Ünal E, Kocaay P, Guran T, Buyukyilmaz G, Ugurlu AK, Tosun BG, Turan I, Kurnaz E, Yuksel B, Turkkahraman D, Cayir A, Celmeli G, Gonc EN, Eklioğlu BS, Cetinkaya S, Yilmaz SK, Atabek ME, Buyukinan M, Arslan E, Mengen E, Cakir EDP, Karaoglan M, Hatipoglu N, Orbak Z, Ucar A, Akyurek N, Akbas ED, Isik E, Kaygusuz SB, Sutcu ZK, Seymen G, Berberoglu M. Siklar Z, et al. Among authors: mengen e. Endocrine. 2024 Sep;85(3):1407-1416. doi: 10.1007/s12020-024-03962-6. Epub 2024 Jul 17. Endocrine. 2024. PMID: 39020240 Free PMC article.
Enzyme Replacement Therapy in Hypophosphatasia.
Uçaktürk SA, Elmaogullari S, Ünal S, Gönülal D, Mengen E. Uçaktürk SA, et al. Among authors: mengen e. J Coll Physicians Surg Pak. 2018 Sep;28(9):S198-S200. doi: 10.29271/jcpsp.2018.09.S198. J Coll Physicians Surg Pak. 2018. PMID: 30173697
CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.
Turan I, Hutchins BI, Hacihamdioglu B, Kotan LD, Gurbuz F, Ulubay A, Mengen E, Yuksel B, Wray S, Topaloglu AK. Turan I, et al. Among authors: mengen e. J Clin Endocrinol Metab. 2017 Jun 1;102(6):1816-1825. doi: 10.1210/jc.2016-3391. J Clin Endocrinol Metab. 2017. PMID: 28324054 Free PMC article.
Mutations in FEZF1 cause Kallmann syndrome.
Kotan LD, Hutchins BI, Ozkan Y, Demirel F, Stoner H, Cheng PJ, Esen I, Gurbuz F, Bicakci YK, Mengen E, Yuksel B, Wray S, Topaloglu AK. Kotan LD, et al. Among authors: mengen e. Am J Hum Genet. 2014 Sep 4;95(3):326-31. doi: 10.1016/j.ajhg.2014.08.006. Am J Hum Genet. 2014. PMID: 25192046 Free PMC article.
Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.
Akkuş G, Kotan LD, Durmaz E, Mengen E, Turan İ, Ulubay A, Gürbüz F, Yüksel B, Tetiker T, Topaloğlu AK. Akkuş G, et al. Among authors: mengen e. J Clin Res Pediatr Endocrinol. 2017 Jun 1;9(2):95-100. doi: 10.4274/jcrpe.3908. Epub 2016 Dec 23. J Clin Res Pediatr Endocrinol. 2017. PMID: 28008864 Free PMC article.
Catecholamine-induced Myocarditis in a Child with Pheochromocytoma.
Uçaktürk SA, Mengen E, Azak E, Çetin İİ, Kocaay P, Şenel E. Uçaktürk SA, et al. Among authors: mengen e. J Clin Res Pediatr Endocrinol. 2020 Jun 3;12(2):202-205. doi: 10.4274/jcrpe.galenos.2019.2019.0045. Epub 2019 Jun 18. J Clin Res Pediatr Endocrinol. 2020. PMID: 31208160 Free PMC article.
41 results