Kiraz A - Search Results

1

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

2

Are MUC5B and TERT mutations genetic risk factors for pulmonary fibrosis in individuals with severe COVID-19?

Yetkin NA, Kiraz A, Baran Ketencioğlu B, Bol C, Tutar N. Yetkin NA, et al. Among authors: kiraz a. Tuberk Toraks. 2023 Mar;71(1):34-40. doi: 10.5578/tt.20239905. Tuberk Toraks. 2023. PMID: 36912407 Free PMC article.

3

Osteopontin as an early predictor of atherosclerosis in attack-free Familial Mediterranean fever patients.

Baspinar O, Kocer D, Kiraz A, Tokmak TT, Dizdar OS. Baspinar O, et al. Among authors: kiraz a. Medicine (Baltimore). 2023 Sep 29;102(39):e35137. doi: 10.1097/MD.0000000000035137. Medicine (Baltimore). 2023. PMID: 37773839 Free PMC article.

4

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

5

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

6

Wiedemann-Rautenstrauch syndrome: report of a variant case.

Kiraz A, Ozen S, Tubas F, Usta Y, Aldemir O, Alanay Y. Kiraz A, et al. Am J Med Genet A. 2012 Jun;158A(6):1434-6. doi: 10.1002/ajmg.a.35336. Epub 2012 May 14. Am J Med Genet A. 2012. PMID: 22585414

7

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.

8

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

9

Three patients resembling Teebi-Shaltout syndrome.

Aldemir O, Ozen S, Erdem S, Kiraz A, Akarsu N, Alanay Y. Aldemir O, et al. Among authors: kiraz a. Am J Med Genet A. 2013 Oct;161A(10):2570-5. doi: 10.1002/ajmg.a.36082. Epub 2013 Aug 5. Am J Med Genet A. 2013. PMID: 23918592

10

Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients.

Akalin H, Sahin IO, Paskal SA, Tan B, Yalcinkaya E, Demir M, Yakubi M, Caliskan BO, Ekinci OG, Ercan M, Kucuk TY, Gokgoz G, Kiraz A, Per H, Ozgun MT, Baydilli N, Ozkul Y, Dundar M. Akalin H, et al. Among authors: kiraz a. J Clin Lab Anal. 2024 Jan;38(1-2):e24997. doi: 10.1002/jcla.24997. Epub 2023 Dec 19. J Clin Lab Anal. 2024. PMID: 38115218 Free PMC article.

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