Yıldırım MS - Search Results

1

NAT2 Gene Polymorphisms in Turkish Patients with Psoriasis Vulgaris.

Dursun R, Dursun HG, Zamani AG, Yıldırım MS, Çınar İ. Dursun R, et al. Among authors: yildirim ms. Biomed Res Int. 2018 Jun 11;2018:3258708. doi: 10.1155/2018/3258708. eCollection 2018. Biomed Res Int. 2018. PMID: 29992137 Free PMC article.

2

Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion.

Zamani AG, Acar A, Durakbasi-Dursun G, Yildirim MS, Ceylaner S, Tuncez E. Zamani AG, et al. Among authors: yildirim ms. Am J Med Genet A. 2014 May;164A(5):1239-44. doi: 10.1002/ajmg.a.36410. Epub 2014 Jan 29. Am J Med Genet A. 2014. PMID: 24478222

3

Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome.

Bayram Y, Pehlivan D, Karaca E, Gambin T, Jhangiani SN, Erdin S, Gonzaga-Jauregui C, Wiszniewski W, Muzny D; Baylor-Hopkins Center for Mendelian Genomics; Elcioglu NH, Yildirim MS, Bozkurt B, Zamani AG, Boerwinkle E, Gibbs RA, Lupski JR. Bayram Y, et al. Among authors: yildirim ms. Am J Med Genet A. 2014 Sep;164A(9):2328-34. doi: 10.1002/ajmg.a.36678. Epub 2014 Jul 14. Am J Med Genet A. 2014. PMID: 25045128 Free PMC article.

4

Association of Apolipoprotein E Polymorphism with Intravitreal Ranibizumab Treatment Outcomes in Age-Related Macular Degeneration.

Bakbak B, Ozturk BT, Zamani AG, Gonul S, Iyit N, Gedik S, Yıldırım MS. Bakbak B, et al. Among authors: yildirim ms. Curr Eye Res. 2016 Jun;41(6):862-6. doi: 10.3109/02713683.2015.1067325. Epub 2015 Sep 23. Curr Eye Res. 2016. PMID: 26398858

5

Would mean platelet volume/platelet count ratio be used as a novel formula to predict 22q11.2 deletion syndrome?

Gokturk B, Guner SN, Kara R, Kirac M, Keles S, Artac H, Zamani AG, Yildirim MS, Reisli I. Gokturk B, et al. Among authors: yildirim ms. Asian Pac J Allergy Immunol. 2016 Jun;34(2):166-73. doi: 10.12932/AP0604.34.2.2016. Asian Pac J Allergy Immunol. 2016. PMID: 27007839 Free article.

6

A rare case in literature: Isochromosome Xq in Klinefelter syndrome.

Simsek L, Zamani AG, Taskapu HH, Yildirim MS. Simsek L, et al. Among authors: yildirim ms. Andrologia. 2019 Jun;51(5):e13253. doi: 10.1111/and.13253. Epub 2019 Feb 11. Andrologia. 2019. PMID: 30746732

7

Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C].

Anlıaçık SÖ, Tokgöz S, Zamani AG, Yıldırım MS, İyisoy MS. Anlıaçık SÖ, et al. Among authors: yildirim ms. Turk J Med Sci. 2019 Apr 18;49(2):589-594. doi: 10.3906/sag-1808-57. Turk J Med Sci. 2019. PMID: 30997974 Free PMC article.

8

A Novel Pathogenic Variant of the CFTR Gene in a Patient with Cystic Fibrosis Phenotype-c.4096A > T.

Arslan AB, Zamani AG, Pekcan S, Yıldırım MS. Arslan AB, et al. Among authors: yildirim ms. J Pediatr Genet. 2020 Mar;9(1):40-43. doi: 10.1055/s-0039-1694964. Epub 2019 Aug 28. J Pediatr Genet. 2020. PMID: 31976142 Free PMC article.

9

Interchromosomal effect: Report of a father and son, bearing different translocations of the same chromosome, and a review of the current literature.

Yıldırım MS, Arslan AB, Zamani AG. Yıldırım MS, et al. Andrologia. 2021 Feb;53(1):e13805. doi: 10.1111/and.13805. Epub 2020 Aug 30. Andrologia. 2021. PMID: 32862490 Review.

10

Novel findings, mini-review and dysmorphological characterization of 16p13.11 microduplication syndrome.

Arslan AB, Zamani AG, Yıldırım MS. Arslan AB, et al. Among authors: yildirim ms. Int J Dev Neurosci. 2022 Jun;82(4):289-294. doi: 10.1002/jdn.10188. Epub 2022 May 24. Int J Dev Neurosci. 2022. PMID: 35470466 Review.

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