Catlı G - Search Results

1

Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutations.

Anık A, Kersseboom S, Demir K, Catlı G, Yiş U, Böber E, van Mullem A, van Herebeek RE, Hız S, Abacı A, Visser TJ. Anık A, et al. Among authors: catli g. Horm Res Paediatr. 2014;82(4):261-71. doi: 10.1159/000365191. Epub 2014 Sep 18. Horm Res Paediatr. 2014. PMID: 25247785

2

Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from Turkey.

Catli G, Abaci A, Demir K, Ulusoy E, Altincik A, Buyukgebiz A, Bober E. Catli G, et al. J Pediatr Endocrinol Metab. 2012;25(5-6):499-502. doi: 10.1515/jpem-2012-0006. J Pediatr Endocrinol Metab. 2012. PMID: 22876545

3

Evaluation of neutrophil gelatinase-associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents.

Demir K, Abaci A, Küme T, Altincik A, Catli G, Böber E. Demir K, et al. Among authors: catli g. J Pediatr Endocrinol Metab. 2012;25(5-6):517-23. J Pediatr Endocrinol Metab. 2012. PMID: 22876548

4

Permanent neonatal diabetes caused by a novel mutation in the INS gene.

Catli G, Abaci A, Flanagan SE, Anik A, Ellard S, Bober E. Catli G, et al. Diabetes Res Clin Pract. 2013 Jan;99(1):e5-8. doi: 10.1016/j.diabres.2012.10.009. Epub 2012 Oct 27. Diabetes Res Clin Pract. 2013. PMID: 23107109

5

A case of rapid-onset obesity with hypothalamic dysfunction, hypoventilation, autonomic dysregulation, and neural crest tumor: ROHHADNET syndrome.

Abaci A, Catli G, Bayram E, Koroglu T, Olgun HN, Mutafoglu K, Hiz AS, Cakmakci H, Bober E. Abaci A, et al. Among authors: catli g. Endocr Pract. 2013 Jan-Feb;19(1):e12-6. doi: 10.4158/EP12140.CR. Endocr Pract. 2013. PMID: 23186956

6

Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence.

Catli G, Abaci A, Bober E, Büyükgebiz A. Catli G, et al. J Pediatr Endocrinol Metab. 2013;26(1-2):1-11. doi: 10.1515/jpem-2012-0327. J Pediatr Endocrinol Metab. 2013. PMID: 23327784 Review.

7

Hyperprolactinemia in children: clinical features and long-term results.

Catli G, Abaci A, Altincik A, Demir K, Can S, Buyukgebiz A, Bober E. Catli G, et al. J Pediatr Endocrinol Metab. 2012;25(11-12):1123-8. doi: 10.1515/jpem-2012-0130. J Pediatr Endocrinol Metab. 2012. PMID: 23329759

8

The relation of serum nesfatin-1 level with metabolic and clinical parameters in obese and healthy children.

Abaci A, Catli G, Anik A, Kume T, Bober E. Abaci A, et al. Among authors: catli g. Pediatr Diabetes. 2013 May;14(3):189-95. doi: 10.1111/pedi.12009. Epub 2013 Jan 24. Pediatr Diabetes. 2013. PMID: 23346951

9

Bilateral pheochromocytoma as first manifestation of von Hippel-Lindau disease: a case report.

Catli G, Abaci A, Neumann HC, Altincik A, Demir K, Böber E. Catli G, et al. Turk J Pediatr. 2012 Sep-Oct;54(5):532-5. Turk J Pediatr. 2012. PMID: 23427520

10

A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case report.

Catli G, Abaci A, Flanagan SE, De Franco E, Ellard S, Hattersley A, Guleryuz H, Bober E. Catli G, et al. Diabetes Metab. 2013 Sep;39(4):370-4. doi: 10.1016/j.diabet.2013.01.005. Epub 2013 Apr 30. Diabetes Metab. 2013. PMID: 23639568

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