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Did you mean mengel e[Author] (130 results)?
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
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.
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.
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.
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.
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: mengen e. 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.
32 results