Demir K - Search Results

1

Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey.

Poyrazoğlu Ş, Akçay T, Arslanoğlu İ, Atabek ME, Atay Z, Berberoğlu M, Bereket A, Bideci A, Bircan İ, Böber E, Can Ş, Cesur Y, Darcan Ş, Demir K, Dündar B, Ersoy B, Esen İ, Güven A, Kara C, Keskin M, Kurtoğlu S, Memioğlu N, Özbek MN, Özgen T, Sarı E, Şıklar Z, Şimşek E, Turan S, Yeşilkaya E, Yüksel B, Darendeliler F. Poyrazoğlu Ş, et al. Among authors: demir k. J Clin Res Pediatr Endocrinol. 2015 Mar;7(1):37-44. doi: 10.4274/jcrpe.1794. J Clin Res Pediatr Endocrinol. 2015. PMID: 25800474 Free PMC article.

2

A non-endocrine cause of testicular enlargement mimicking precocious puberty: testicular microlithiasis.

Bober E, Dundar B, Demir K, Abaci A, Cakmakçi H, Buyukgebiz A. Bober E, et al. Among authors: demir k. J Pediatr Endocrinol Metab. 2007 Nov;20(11):1237-40. doi: 10.1515/jpem.2007.20.11.1237. J Pediatr Endocrinol Metab. 2007. PMID: 18183796

3

Endocrine disrupters - with special emphasis on sexual development.

Abaci A, Demir K, Bober E, Buyukgebiz A. Abaci A, et al. Among authors: demir k. Pediatr Endocrinol Rev. 2009 Jun;6(4):464-75. Pediatr Endocrinol Rev. 2009. PMID: 19550381 Review.

4

A comparison of multiple daily insulin therapy with continuous subcutaneous insulin infusion therapy in adolescents with type 1 diabetes mellitus: a single-center experience from Turkey.

Abaci A, Atas A, Unuvar T, Demir K, Bober E, Büyükgebiz A. Abaci A, et al. Among authors: demir k. J Pediatr Endocrinol Metab. 2009 Jun;22(6):539-45. doi: 10.1515/jpem.2009.22.6.539. J Pediatr Endocrinol Metab. 2009. PMID: 19694201

5

A novel mutation in the AVPR2 gene (222delA) associated with X-linked nephrogenic diabetes insipidus in a boy with growth failure.

Abaci A, Wood K, Demir K, Büyükgebiz A, Böber E, Kopp P. Abaci A, et al. Among authors: demir k. Endocr Pract. 2010 Mar-Apr;16(2):231-6. doi: 10.4158/EP09165.CR. Endocr Pract. 2010. PMID: 19703807

6

Metabolic alterations during valproic acid treatment: a prospective study.

Abaci A, Saygi M, Yis U, Demir K, Dirik E, Bober E. Abaci A, et al. Among authors: demir k. Pediatr Neurol. 2009 Dec;41(6):435-9. doi: 10.1016/j.pediatrneurol.2009.06.003. Pediatr Neurol. 2009. PMID: 19931165

7

A 2-year-old boy with a testicular mass. Diagnosis: testicular tumor of adrenogenital syndrome due to 11-beta-hydroxylase deficiency.

Unuvar T, Demir K, Abaci A, Atas A, Cakmakci H, Bober E. Unuvar T, et al. Among authors: demir k. Pediatr Ann. 2010 Aug;39(8):471-4. doi: 10.3928/00904481-20100726-04. Pediatr Ann. 2010. PMID: 20704142 No abstract available.

8

A mother and son with Noonan syndrome resulting from a PTPN11 mutation: first report of molecularly proven cases from Turkey.

Demir K, Yntema HG, Altincik A, Böber E. Demir K, et al. Turk J Pediatr. 2010 May-Jun;52(3):321-4. Turk J Pediatr. 2010. PMID: 20718194

9

Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.

Cangul H, Morgan NV, Forman JR, Saglam H, Aycan Z, Yakut T, Gulten T, Tarim O, Bober E, Cesur Y, Kirby GA, Pasha S, Karkucak M, Eren E, Cetinkaya S, Bas V, Demir K, Yuca SA, Meyer E, Kendall M, Hogler W, Barrett TG, Maher ER. Cangul H, et al. Among authors: demir k. Clin Endocrinol (Oxf). 2010 Nov;73(5):671-7. doi: 10.1111/j.1365-2265.2010.03849.x. Clin Endocrinol (Oxf). 2010. PMID: 20718767

10

Tamoxifen as first-line treatment in a premenarchal girl with juvenile breast hypertrophy.

Demir K, Unuvar T, Eren S, Abaci A, Bober E. Demir K, et al. J Pediatr Adolesc Gynecol. 2010 Oct;23(5):e133-6. doi: 10.1016/j.jpag.2009.11.003. J Pediatr Adolesc Gynecol. 2010. PMID: 20813327

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