Kiraz A - Search Results

1

Thyroid hypoplasia as a cause of congenital hypothyroidism in monozygotic twins concordant for Rubinstein-Taybi syndrome.

Akın MA, Güneş T, Akın L, Çoban D, Oncu SK, Kiraz A, Kurtoğlu S. Akın MA, et al. Among authors: kiraz a. J Clin Res Pediatr Endocrinol. 2011;3(1):32-5. doi: 10.4274/jcrpe.v3i1.07. Epub 2011 Feb 23. J Clin Res Pediatr Endocrinol. 2011. PMID: 21448332 Free PMC article.

2

Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome.

Dundar M, Kiraz A, Tasdemir S, Akalin H, Kurtoglu S, Hafo F, Cine N, Savli H. Dundar M, et al. Among authors: kiraz a. Am J Med Genet A. 2010 Nov;152A(11):2791-5. doi: 10.1002/ajmg.a.33249. Am J Med Genet A. 2010. PMID: 20949503

3

Asymmetric crying face in a newborn with isotretinoin embryopathy.

Sarici D, Akin MA, Kurtoglu S, Uzum K, Kiraz A. Sarici D, et al. Among authors: kiraz a. Pediatr Dermatol. 2013 Nov-Dec;30(6):e289-90. doi: 10.1111/j.1525-1470.2012.01743.x. Epub 2012 May 21. Pediatr Dermatol. 2013. PMID: 22612313

4

TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis.

Cangul H, Aycan Z, Saglam H, Forman JR, Cetinkaya S, Tarim O, Bober E, Cesur Y, Kurtoglu S, Darendeliler F, Bas V, Eren E, Demir K, Kiraz A, Aydin BK, Karthikeyan A, Kendall M, Boelaert K, Shaw NJ, Kirk J, Högler W, Barrett TG, Maher ER. Cangul H, et al. Among authors: kiraz a. J Pediatr Endocrinol Metab. 2012;25(5-6):419-26. doi: 10.1515/jpem-2012-0053. J Pediatr Endocrinol Metab. 2012. PMID: 22876533

5

A NOVEL MUTATION ASSOCIATED WITH NEPHROLITIHASIS IN ELLIS-VAN CREVELD SYNDROME.

Kiraz A, Akin MA, Arslan A, Zabel B, Lausch E. Kiraz A, et al. Genet Couns. 2015;26(3):377-9. Genet Couns. 2015. PMID: 26625674 No abstract available.

6

A patient with hyperphalangism: the milder phenotype of Catel-Manzke syndrome.

Kiraz A, Tubas F, Ekinci Y, Dögen ME, Varli M. Kiraz A, et al. Clin Dysmorphol. 2013 Oct;22(4):169-171. doi: 10.1097/MCD.0000000000000010. Clin Dysmorphol. 2013. PMID: 24326962 No abstract available.

7

Recurrent symptomatic urolithiasis in a patient with cystic fibrosis.

Yel S, Dursun I, Köse M, Kiraz A, Poyrazoglu MH, Dündar M. Yel S, et al. Among authors: kiraz a. Pediatr Nephrol. 2024 Dec;39(12):3467-3469. doi: 10.1007/s00467-024-06433-2. Epub 2024 Jun 25. Pediatr Nephrol. 2024. PMID: 38916781 Free PMC article.

8

A truncating variant in the THOC6 gene with new findings in a patient with Beaulieu-Boycott-Innes syndrome.

Kiraz A, Tubaş F, Seber T. Kiraz A, et al. Am J Med Genet A. 2022 May;188(5):1568-1571. doi: 10.1002/ajmg.a.62667. Epub 2022 Jan 27. Am J Med Genet A. 2022. PMID: 35084103

9

Common Familial Mediterranean Fever gene mutations in a Turkish cohort.

Dundar M, Emirogullari EF, Kiraz A, Taheri S, Baskol M. Dundar M, et al. Among authors: kiraz a. Mol Biol Rep. 2011 Nov;38(8):5065-9. doi: 10.1007/s11033-010-0652-7. Epub 2010 Dec 14. Mol Biol Rep. 2011. PMID: 21153919

10

A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients.

Dundar M, Kiraz A, Emirogullari EF, Saatci CE, Taheri S, Baskol M, Polat S, Ozkul Y. Dundar M, et al. Among authors: kiraz a. Ann Saudi Med. 2012 Jul-Aug;32(4):343-8. doi: 10.5144/0256-4947.2012.343. Ann Saudi Med. 2012. PMID: 22705602 Free PMC article.

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