Berdelİ A - Search Results

1

Blau Syndrome and Early-Onset Sarcoidosis: A Six Case Series and Review of the Literature.

PaÇ Kisaarslan A, SÖzerİ B, Şahİn N, Özdemİr ÇİÇek S, GÜndÜz Z, Demİrkaya E, Berdelİ A, Sadet Özcan S, PorazoĞlu H, DÜŞÜnsel R. PaÇ Kisaarslan A, et al. Among authors: berdeli a. Arch Rheumatol. 2019 Nov 6;35(1):117-127. doi: 10.5606/ArchRheumatol.2020.7060. eCollection 2020 Mar. Arch Rheumatol. 2019. PMID: 32637927 Free PMC article.

2

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. Pediatr Nephrol. 2007 Dec;22(12):2031-40. doi: 10.1007/s00467-007-0595-y. Epub 2007 Sep 25. Pediatr Nephrol. 2007. PMID: 17899208

3

Association between Toll-like receptors 4 and 2 gene polymorphisms with chronic allograft nephropathy in Turkish children.

Mutlubas F, Mir S, Berdeli A, Ozkayin N, Sozeri B. Mutlubas F, et al. Among authors: berdeli a. Transplant Proc. 2009 Jun;41(5):1589-93. doi: 10.1016/j.transproceed.2009.02.079. Transplant Proc. 2009. PMID: 19545686

4

Familial Mediterranean fever gene mutation frequencies and genotype-phenotype correlations in the Aegean region of Turkey.

Ozalkaya E, Mir S, Sozeri B, Berdeli A, Mutlubas F, Cura A. Ozalkaya E, et al. Among authors: berdeli a. Rheumatol Int. 2011 Jun;31(6):779-84. doi: 10.1007/s00296-010-1383-8. Epub 2010 Mar 9. Rheumatol Int. 2011. PMID: 20217092

5

Comprehensive analysis of a large-scale screen for MEFV gene mutations: do they truly provide a "heterozygote advantage" in Turkey?

Berdeli A, Mir S, Nalbantoglu S, Kutukculer N, Sozeri B, Kabasakal Y, Cam S, Solak M. Berdeli A, et al. Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):475-82. doi: 10.1089/gtmb.2010.0146. Epub 2011 Mar 17. Genet Test Mol Biomarkers. 2011. PMID: 21413889

6

TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.

Mir S, Yavascan O, Berdeli A, Sozeri B. Mir S, et al. Among authors: berdeli a. Nephrol Dial Transplant. 2012 Jan;27(1):205-9. doi: 10.1093/ndt/gfr202. Epub 2011 Apr 21. Nephrol Dial Transplant. 2012. PMID: 21511817

7

Gene polymorphism of complement factor H in a Turkish patient with membranoproliferative glomerulonephritis type II.

Sozeri B, Mir S, Berdeli A, Dincel N, Sarsik B. Sozeri B, et al. Among authors: berdeli a. Iran J Kidney Dis. 2012 Mar;6(2):149-53. Iran J Kidney Dis. 2012. PMID: 22388616 Free article.

8

Complement-4 deficiency in a child with systemic lupus erythematosus presenting with standard treatment-resistant severe skin lesion.

Sozeri B, Mir S, Berdeli A. Sozeri B, et al. Among authors: berdeli a. ISRN Rheumatol. 2011;2011:917673. doi: 10.5402/2011/917673. Epub 2011 Feb 10. ISRN Rheumatol. 2011. PMID: 22482068 Free PMC article.

9

Does NPHS1 polymorphism modulate P118l mutation in NPHS2?

Dincel N, Mir S, Berdeli A, Bulut IK, Sozeri B. Dincel N, et al. Among authors: berdeli a. Saudi J Kidney Dis Transpl. 2013 Nov;24(6):1210-3. doi: 10.4103/1319-2442.121300. Saudi J Kidney Dis Transpl. 2013. PMID: 24231487

10

The predictive value of urinary UPIb mRNA levels in VUR and recurrent urinary tract infections.

Bulut IK, Mir S, Berdeli A, Sozeri B. Bulut IK, et al. Among authors: berdeli a. Clin Nephrol. 2014 Mar;81(3):152-8. doi: 10.5414/cn107778. Clin Nephrol. 2014. PMID: 24559587

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