Caglayan S - Search Results

1

Vitamin d-receptor gene polymorphisms and vertebral bone density in men with idiopathic hypogonadotrophic hypogonadism.

Ozisik G, Mergen H, Ozata M, Uyanik C, Caglayan S, Turan M, Bolu E, Ilgin S, Oner R, Ozdemir IC, Oner C. Ozisik G, et al. Among authors: caglayan s. Med Sci Monit. 2001 Mar-Apr;7(2):233-7. Med Sci Monit. 2001. PMID: 11257727

2

Effects of gonadotropin and testosterone treatments on plasma leptin levels in male patients with idiopathic hypogonadotropic hypogonadism and Klinefelter's syndrome.

Ozata M, Ozisik G, Caglayan S, Yesilova Z, Bingöl N, Saglam M, Turan M, Beyhan Z. Ozata M, et al. Among authors: caglayan s. Horm Metab Res. 1998 May;30(5):266-71. doi: 10.1055/s-2007-978881. Horm Metab Res. 1998. PMID: 9660087 Clinical Trial.

3

Plasma melatonin concentration before and during testosterone replacement in Klinefelter's syndrome: relation to hepatic indolamine metabolism and sympathoadrenal activity.

Caglayan S, Ozata M, Ozisik G, Turan M, Bolu E, Oktenli C, Arslan N, Erbil K, Gul D, Ozdemir IC. Caglayan S, et al. J Clin Endocrinol Metab. 2001 Feb;86(2):738-43. doi: 10.1210/jcem.86.2.7225. J Clin Endocrinol Metab. 2001. PMID: 11158039

4

Event-related brain potentials in male hypogonadism.

Ozata M, Odabasi Z, Caglayan S, Beyhan Z, Vural O, Ozdemir C. Ozata M, et al. Among authors: caglayan s. J Endocrinol Invest. 1999 Jul-Aug;22(7):508-13. doi: 10.1007/BF03343601. J Endocrinol Invest. 1999. PMID: 10475147

5

Impact of glucocorticoid receptor gene (NR3C1) polymorphisms in Turkish patients with metabolic syndrome.

Kaya Z, Caglayan S, Akkiprik M, Aral C, Ozisik G, Ozata M, Ozer A. Kaya Z, et al. Among authors: caglayan s. J Endocrinol Invest. 2016 May;39(5):557-66. doi: 10.1007/s40618-015-0409-1. Epub 2015 Nov 23. J Endocrinol Invest. 2016. PMID: 26596278

6

Magnetic resonance imaging of posterior pituitary for evaluation of the neurohypophyseal function in idiopathic and autosomal dominant neurohypophyseal diabetes insipidus.

Ozata M, Tayfun C, Kurtaran K, Yetkin I, Beyhan Z, Corakci A, Cağlayan S, Alemdaroglu A, Gündogan MA. Ozata M, et al. Among authors: caglayan s. Eur Radiol. 1997;7(7):1098-102. doi: 10.1007/s003300050261. Eur Radiol. 1997. PMID: 9265683

7

The effect of subclinical hypothyroidism on platelet parameters.

Erikci AA, Karagoz B, Ozturk A, Caglayan S, Ozisik G, Kaygusuz I, Ozata M. Erikci AA, et al. Among authors: caglayan s. Hematology. 2009 Apr;14(2):115-7. doi: 10.1179/102453309X385124. Hematology. 2009. PMID: 19298725 Free article.

8

Synchronicity of frequently sampled thyrotropin (TSH) and leptin concentrations in healthy adults and leptin-deficient subjects: evidence for possible partial TSH regulation by leptin in humans.

Mantzoros CS, Ozata M, Negrao AB, Suchard MA, Ziotopoulou M, Caglayan S, Elashoff RM, Cogswell RJ, Negro P, Liberty V, Wong ML, Veldhuis J, Ozdemir IC, Gold PW, Flier JS, Licinio J. Mantzoros CS, et al. Among authors: caglayan s. J Clin Endocrinol Metab. 2001 Jul;86(7):3284-91. doi: 10.1210/jcem.86.7.7644. J Clin Endocrinol Metab. 2001. PMID: 11443202

9

Investigation of relationship of the mitochondrial DNA 16189 T>C polymorphism with metabolic syndrome and its associated clinical parameters in Turkish patients.

Aral C, Akkiprik M, Caglayan S, Atabey Z, Ozişik G, Bekiroglu N, Ozer A. Aral C, et al. Among authors: caglayan s. Hormones (Athens). 2011 Oct-Dec;10(4):298-303. doi: 10.14310/horm.2002.1321. Hormones (Athens). 2011. PMID: 22281886 Free article.

10

Mitochondrial DNA common deletion is not associated with thyroid, breast and colorectal tumors in Turkish patients.

Aral C, Akkiprik M, Kaya H, Ataizi-Çelikel C, Caglayan S, Ozisik G, Baloglu H, Ozer A. Aral C, et al. Among authors: caglayan s. Genet Mol Biol. 2010 Jan;33(1):1-4. doi: 10.1590/S1415-47572009005000102. Epub 2010 Mar 1. Genet Mol Biol. 2010. PMID: 21637595 Free PMC article.

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