Tabel Y - Search Results

1

Is presence of hypertension in obese children correlate with the criteria of metabolic syndrome?

Mir S, Tabel Y, Darcan S. Mir S, et al. Among authors: tabel y. J Trop Pediatr. 2007 Dec;53(6):424-7. doi: 10.1093/tropej/fmm057. Epub 2007 Jun 27. J Trop Pediatr. 2007. PMID: 17596290

2

Correction to: Adolescence‑onset atypical hemolytic uremic syndrome: is it different from infant‑onset?

Celegen K, Gulhan B, Fidan K, Yuksel S, Yilmaz N, Yılmaz AC, Demircioğlu Kılıç B, Gokce I, Kavaz Tufan A, Kalyoncu M, Nalcacıoglu H, Ozlu SG, Kurt Sukur ED, Canpolat N, K Bayazit A, Çomak E, Tabel Y, Tulpar S, Celakil M, Bek K, Zeybek C, Duzova A, Özçakar ZB, Topaloglu R, Soylemezoglu O, Ozaltin F. Celegen K, et al. Among authors: tabel y. Clin Exp Nephrol. 2024 Oct;28(10):1038-1039. doi: 10.1007/s10157-024-02520-8. Clin Exp Nephrol. 2024. PMID: 38970651 No abstract available.

3

Association of macrophage migration inhibitory factor -173C allele polymorphism with steroid resistance in children with nephrotic syndrome.

Berdeli A, Mir S, Ozkayin N, Serdaroglu E, Tabel Y, Cura A. Berdeli A, et al. Among authors: tabel y. Pediatr Nephrol. 2005 Nov;20(11):1566-71. doi: 10.1007/s00467-005-1930-9. Epub 2005 Aug 16. Pediatr Nephrol. 2005. PMID: 16133063

4

Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome.

Tabel Y, Berdeli A, Mir S, Serdaroğlu E, Yilmaz E. Tabel Y, et al. J Renin Angiotensin Aldosterone Syst. 2005 Dec;6(3):138-44. doi: 10.3317/jraas.2005.020. J Renin Angiotensin Aldosterone Syst. 2005. PMID: 16525944 Free article.

5

NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.

Berdeli A, Mir S, Yavascan O, Serdaroglu E, Bak M, Aksu N, Oner A, Anarat A, Donmez O, Yildiz N, Sever L, Tabel Y, Dusunsel R, Sonmez F, Cakar N. Berdeli A, et al. Among authors: tabel y. Pediatr Nephrol. 2007 Dec;22(12):2031-40. doi: 10.1007/s00467-007-0595-y. Epub 2007 Sep 25. Pediatr Nephrol. 2007. PMID: 17899208

6

Association of TLR2 gene Arg753Gln polymorphism with urinary tract infection in children.

Tabel Y, Berdeli A, Mir S. Tabel Y, et al. Int J Immunogenet. 2007 Dec;34(6):399-405. doi: 10.1111/j.1744-313X.2007.00709.x. Int J Immunogenet. 2007. PMID: 18001294

7

The long-term outcomes of idiopathic hypercalciuria in children.

Tabel Y, Mir S. Tabel Y, et al. J Pediatr Urol. 2006 Oct;2(5):453-8. doi: 10.1016/j.jpurol.2005.10.009. Epub 2005 Dec 5. J Pediatr Urol. 2006. PMID: 18947655

8

Interleukin 8 gene 2767 A/G polymorphism is associated with increased risk of nephritis in children with Henoch-Schönlein purpura.

Tabel Y, Mir S, Berdeli A. Tabel Y, et al. Rheumatol Int. 2012 Apr;32(4):941-7. doi: 10.1007/s00296-010-1739-0. Epub 2011 Jan 15. Rheumatol Int. 2012. PMID: 21240497

9

Association between RAS gene polymorphisms (ACE I/D, AGT M235T) and Henoch-Schönlein purpura in a Turkish population.

Nalbantoglu S, Tabel Y, Mir S, Serdaroğlu E, Berdeli A. Nalbantoglu S, et al. Among authors: tabel y. Dis Markers. 2013;34(1):23-32. doi: 10.3233/DMA-2012-120946. Dis Markers. 2013. PMID: 23151617 Free PMC article.

10

Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients.

Nalbantoglu S, Tabel Y, Mir S, Berdeli A. Nalbantoglu S, et al. Among authors: tabel y. Cytokine. 2013 Apr;62(1):160-4. doi: 10.1016/j.cyto.2013.02.024. Epub 2013 Mar 20. Cytokine. 2013. PMID: 23523092

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