Kiraz A - Search Results

1

The role of TNF-α and PAI-1 gene polymorphisms in familial Mediterranean fever.

Dundar M, Kiraz A, Balta B, Emirogullari EF, Zararsiz G, Yurci A, Aslan D, Baskol M. Dundar M, et al. Among authors: kiraz a. Mod Rheumatol. 2013 Jan;23(1):140-5. doi: 10.1007/s10165-012-0687-9. Epub 2012 Jun 27. Mod Rheumatol. 2013. PMID: 22736074

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

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

4

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.

5

A new finding in a patient with Mowat Wilson syndrome: peripupillary atrophy and gingival hypertrophy.

Kiraz A, Aldemir O, Karabulut Y, Turan C, Dundar M. Kiraz A, et al. Genet Couns. 2013;24(1):61-8. Genet Couns. 2013. PMID: 23610866

6

Does thiol-disulphide balance show oxidative stress in different MEFV mutations?

Balta B, Erdogan M, Alisik M, Kiraz A, Akalin T, Bastug F, Erel O. Balta B, et al. Among authors: kiraz a. Rheumatol Int. 2018 Jan;38(1):97-104. doi: 10.1007/s00296-017-3914-z. Epub 2017 Dec 19. Rheumatol Int. 2018. PMID: 29260407

7

Decreased disulphide/thiol ratio in patients with autosomal recessive non-syndromic hearing loss.

Balta B, Gundogdu R, Erdogan M, Alisik M, Kiraz A, Ozcan I, Erel O. Balta B, et al. Among authors: kiraz a. Int J Pediatr Otorhinolaryngol. 2018 Sep;112:188-192. doi: 10.1016/j.ijporl.2018.07.014. Epub 2018 Jul 10. Int J Pediatr Otorhinolaryngol. 2018. PMID: 30055731

8

Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G.

Balta B, Erdoğan M, Kiraz A, Korkmaz S, Ağadayı A. Balta B, et al. Among authors: kiraz a. Turk J Haematol. 2019 Feb 7;36(1):25-28. doi: 10.4274/tjh.galenos.2018.2018.0194. Epub 2018 Nov 6. Turk J Haematol. 2019. PMID: 30401656 Free PMC article.

9

A comprehensive molecular analysis and genotype-phenotype correlation in patients with familial mediterranean fever.

Balta B, Erdogan M, Kiraz A, Akalın T, Baştug F, Bayram A. Balta B, et al. Among authors: kiraz a. Mol Biol Rep. 2020 Mar;47(3):1835-1843. doi: 10.1007/s11033-020-05277-x. Epub 2020 Jan 27. Mol Biol Rep. 2020. PMID: 31989427

10

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey.

Erdoğan M, Köse M, Pekcan S, Hangül M, Balta B, Kiraz A, Akıncı Gönen G, Zamani AG, Yıldırım MS, Ramaslı Gürsoy T, Ezgu F, Şişmanlar Eyüpoğlu T, Tana Aslan A. Erdoğan M, et al. Among authors: kiraz a. Balkan Med J. 2021 Nov;38(6):357-364. doi: 10.5152/balkanmedj.2021.21199. Balkan Med J. 2021. PMID: 34860163 Free PMC article.

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