Berdeli A - Search Results

1

Proinflammatory cytokines, prostaglandins and zinc in febrile convulsions.

Tütüncüoğlu S, Kütükçüler N, Kepe L, Coker C, Berdeli A, Tekgül H. Tütüncüoğlu S, et al. Among authors: berdeli a. Pediatr Int. 2001 Jun;43(3):235-9. doi: 10.1046/j.1442-200x.2001.01389.x. Pediatr Int. 2001. PMID: 11380915

2

Fc gamma RIIa, IIIa and IIIb polymorphisms in Turkish children susceptible to recurrent infectious diseases.

Ozturk C, Aksu G, Berdeli A, Kutukculer N. Ozturk C, et al. Among authors: berdeli a. Clin Exp Med. 2006 Mar;6(1):27-32. doi: 10.1007/s10238-006-0090-y. Clin Exp Med. 2006. PMID: 16550341

3

Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections.

Kutukculer N, Yeniay BS, Aksu G, Berdeli A. Kutukculer N, et al. Among authors: berdeli a. Biochem Genet. 2007 Aug;45(7-8):507-14. doi: 10.1007/s10528-007-9091-0. Epub 2007 Jun 7. Biochem Genet. 2007. PMID: 17554618

4

A novel Y331X nonsense mutation in TNFRSF1A gene in two unrelated Turkish families with periodic fever syndrome.

Kutukculer N, Gulez N, Karaca N, Aksu G, Berdeli A. Kutukculer N, et al. Among authors: berdeli a. Int J Immunogenet. 2010 Feb;37(1):21-5. doi: 10.1111/j.1744-313X.2009.00884.x. Epub 2009 Oct 5. Int J Immunogenet. 2010. PMID: 19804406

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

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis.

Gulez N, Aksu G, Berdeli A, Karaca N, Tanrıverdi S, Kutukculer N, Azarsiz E. Gulez N, et al. Among authors: berdeli a. Case Rep Med. 2011;2011:121258. doi: 10.1155/2011/121258. Epub 2011 Apr 12. Case Rep Med. 2011. PMID: 21541208 Free PMC article.

7

Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency.

Kutukculer N, Gulez N, Karaca NE, Aksu G, Berdeli A. Kutukculer N, et al. Among authors: berdeli a. Ital J Pediatr. 2012 Mar 16;38:8. doi: 10.1186/1824-7288-38-8. Ital J Pediatr. 2012. PMID: 22424479 Free PMC article.

8

Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.

Kutukculer N, Gulez N, Karaca NE, Aksu G, Berdeli A. Kutukculer N, et al. Among authors: berdeli a. J Clin Immunol. 2012 Dec;32(6):1165-79. doi: 10.1007/s10875-012-9717-9. Epub 2012 Jun 15. J Clin Immunol. 2012. PMID: 22699762

9

Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections.

Kutukculer N, Azarsiz E, Karaca NE, Aksu G, Berdeli A. Kutukculer N, et al. Among authors: berdeli a. Asian Pac J Allergy Immunol. 2015 Dec;33(4):312-9. doi: 10.12932/AP0586.33.4.2015. Asian Pac J Allergy Immunol. 2015. PMID: 26708396 Free article.

10

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis.

Ulusoy E, Karaca NE, Azarsiz E, Berdeli A, Aksu G, Kutukculer N. Ulusoy E, et al. Among authors: berdeli a. J Clin Med Res. 2016 May;8(5):379-84. doi: 10.14740/jocmr2316w. Epub 2016 Mar 20. J Clin Med Res. 2016. PMID: 27081423 Free PMC article.

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