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Page 1
Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia.
Eachus H, Zaucker A, Oakes JA, Griffin A, Weger M, Güran T, Taylor A, Harris A, Greenfield A, Quanson JL, Storbeck KH, Cunliffe VT, Müller F, Krone N. Eachus H, et al. Among authors: guran t. Endocrinology. 2017 Dec 1;158(12):4165-4173. doi: 10.1210/en.2017-00549. Endocrinology. 2017. PMID: 28938470 Free PMC article.
Predictors of surgical complications in boys with hypospadias: data from an internationa registry.
Scougall K, Bryce J, Baronio F, Boal RL, Castera JR, Castro S, Cheetham T, Costa EC, Darendeliler F, Davies JH, Dirlewanger M, Gazdagh G, Globa E, Guerra-Junior G, Guran T, Herrmann G, Holterhus PM, Akgül AK, Markosyan R, McElreavey K, Miranda ML, Nordenstrom A, O'Toole S, Poyrazoglu S, Russo G, Schwitzgebel V, Stancampiano M, Steigert M, Ahmed SF, Lucas-Herald AK. Scougall K, et al. Among authors: guran t. World J Pediatr Surg. 2023 Oct 11;6(4):e000599. doi: 10.1136/wjps-2023-000599. eCollection 2023. World J Pediatr Surg. 2023. PMID: 37860275 Free PMC article.
Novel associations in disorders of sex development: findings from the I-DSD Registry.
Cox K, Bryce J, Jiang J, Rodie M, Sinnott R, Alkhawari M, Arlt W, Audi L, Balsamo A, Bertelloni S, Cools M, Darendeliler F, Drop S, Ellaithi M, Guran T, Hiort O, Holterhus PM, Hughes I, Krone N, Lisa L, Morel Y, Soder O, Wieacker P, Ahmed SF. Cox K, et al. Among authors: guran t. J Clin Endocrinol Metab. 2014 Feb;99(2):E348-55. doi: 10.1210/jc.2013-2918. Epub 2013 Dec 3. J Clin Endocrinol Metab. 2014. PMID: 24302751 Free PMC article.
Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort.
Guran T, Buonocore F, Saka N, Ozbek MN, Aycan Z, Bereket A, Bas F, Darcan S, Bideci A, Guven A, Demir K, Akinci A, Buyukinan M, Aydin BK, Turan S, Agladioglu SY, Atay Z, Abali ZY, Tarim O, Catli G, Yuksel B, Akcay T, Yildiz M, Ozen S, Doger E, Demirbilek H, Ucar A, Isik E, Ozhan B, Bolu S, Ozgen IT, Suntharalingham JP, Achermann JC. Guran T, et al. J Clin Endocrinol Metab. 2016 Jan;101(1):284-92. doi: 10.1210/jc.2015-3250. Epub 2015 Nov 2. J Clin Endocrinol Metab. 2016. PMID: 26523528 Free PMC article.
Birth Weight in Different Etiologies of Disorders of Sex Development.
Poyrazoglu S, Darendeliler F, Ahmed SF, Hughes I, Bryce J, Jiang J, Rodie M, Hiort O, Hannema SE, Bertelloni S, Lisa L, Guran T, Cools M, Desloovere A, Claahsen-van der Grinten HL, Nordenstrom A, Holterhus PM, Kohler B, Niedziela M, Krone N. Poyrazoglu S, et al. Among authors: guran t. J Clin Endocrinol Metab. 2017 Mar 1;102(3):1044-1050. doi: 10.1210/jc.2016-3460. J Clin Endocrinol Metab. 2017. PMID: 28359094 Free article.
Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height.
Savaş-Erdeve Ş, Çetinkaya S, Abalı ZY, Poyrazoğlu Ş, Baş F, Berberoğlu M, Sıklar Z, Korkmaz Ö, Buluş D, Akbaş ED, Güran T, Böber E, Akın O, Yılmaz GC, Aycan Z. Savaş-Erdeve Ş, et al. Among authors: guran t. J Pediatr Endocrinol Metab. 2017 Jul 26;30(7):759-766. doi: 10.1515/jpem-2017-0088. J Pediatr Endocrinol Metab. 2017. PMID: 28672743
173 results