Bircan I - Search Results

1

Novel human pathological mutations. Gene symbol: TPO. Disease: Thyroid peroxidase deficiency.

Alper O, Turkkahraman D, Bircan I, Luleci G. Alper O, et al. Among authors: bircan i. Hum Genet. 2010 Jan;127(1):120. Hum Genet. 2010. PMID: 20108397 No abstract available.

2

Final diagnosis in children with subclinical hypothyroidism and mutation analysis of the thyroid peroxidase gene (TPO).

Turkkahraman D, Alper OM, Aydin F, Yildiz A, Pehlivanoglu S, Luleci G, Akcurin S, Bircan I. Turkkahraman D, et al. Among authors: bircan i. J Pediatr Endocrinol Metab. 2009 Sep;22(9):845-51. doi: 10.1515/jpem.2009.22.9.845. J Pediatr Endocrinol Metab. 2009. PMID: 19960894 Clinical Trial.

3

Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.

Turkkahraman D, Alper OM, Pehlivanoglu S, Aydin F, Yildiz A, Luleci G, Akcurin S, Bircan I. Turkkahraman D, et al. Among authors: bircan i. Endocrine. 2010 Feb;37(1):124-8. doi: 10.1007/s12020-009-9280-1. Epub 2009 Nov 17. Endocrine. 2010. PMID: 20963560

4

Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene.

Mihci E, Türkkahraman D, Ellard S, Akçurin S, Bircan I. Mihci E, et al. Among authors: bircan i. J Clin Res Pediatr Endocrinol. 2012 Jun;4(2):101-3. doi: 10.4274/jcrpe.619. J Clin Res Pediatr Endocrinol. 2012. PMID: 22672868 Free PMC article.

5

Successful management of primary hypomagnesaemia with high-dose oral magnesium citrate: a case report.

Bircan I, Turkkahraman D, Dursun O, Karaguzel G. Bircan I, et al. Acta Paediatr. 2006 Dec;95(12):1697-9. doi: 10.1080/08035250600750098. Acta Paediatr. 2006. PMID: 17129989

6

Prevalence and risk factors of obesity in school children in Antalya, Turkey.

Turkkahraman D, Bircan I, Tosun O, Saka O. Turkkahraman D, et al. Among authors: bircan i. Saudi Med J. 2006 Jul;27(7):1028-33. Saudi Med J. 2006. PMID: 16830025

7

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A).

Çelmeli G, Türkkahraman D, Çürek Y, Houghton J, Akçurin S, Bircan İ. Çelmeli G, et al. Among authors: bircan i. J Clin Res Pediatr Endocrinol. 2017 Mar 1;9(1):80-84. doi: 10.4274/jcrpe.2894. Epub 2016 Jul 27. J Clin Res Pediatr Endocrinol. 2017. PMID: 27468121 Free PMC article.

8

Type 1 diabetes-related epidemiological, clinical and laboratory findings. An evaluation with special regard to autoimmunity in children.

Karaguzel G, Ozer S, Akcurin S, Turkkahraman D, Bircan I. Karaguzel G, et al. Among authors: bircan i. Saudi Med J. 2007 Apr;28(4):584-9. Saudi Med J. 2007. PMID: 17457482

9

Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapy.

Turkkahraman D, Bircan I, Tribble ND, Akçurin S, Ellard S, Gloyn AL. Turkkahraman D, et al. Among authors: bircan i. J Pediatr. 2008 Jul;153(1):122-6. doi: 10.1016/j.jpeds.2007.12.037. Epub 2008 Mar 6. J Pediatr. 2008. PMID: 18571549

10

A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree.

Durmaz E, Turkkahraman D, Berdeli A, Atan M, Karaguzel G, Akcurin S, Bircan I. Durmaz E, et al. Among authors: bircan i. J Pediatr Endocrinol Metab. 2013;26(5-6):551-5. doi: 10.1515/jpem-2012-0086. J Pediatr Endocrinol Metab. 2013. PMID: 23585174

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