Karaca NE - Search Results

1

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: karaca ne. 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.

2

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia.

Karaca NE, Aksu G, Yeniay BS, Kutukculer N. Karaca NE, et al. Rheumatol Int. 2006 Dec;27(2):179-82. doi: 10.1007/s00296-006-0191-7. Epub 2006 Aug 30. Rheumatol Int. 2006. PMID: 16944159

3

Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency.

Kutukculer N, Karaca NE, Demircioglu O, Aksu G. Kutukculer N, et al. Among authors: karaca ne. Pediatr Allergy Immunol. 2007 Mar;18(2):167-73. doi: 10.1111/j.1399-3038.2006.00491.x. Pediatr Allergy Immunol. 2007. PMID: 17338791

4

Juvenile psoriatic arthritis carrying familial Mediterranean fever gene mutations in a 14-year-old Turkish girl.

Yeniay BS, Karaca NE, Yuksel SE, Midyat L, Kutukculer N. Yeniay BS, et al. Among authors: karaca ne. J Dermatol. 2007 May;34(5):344-8. doi: 10.1111/j.1346-8138.2007.00285.x. J Dermatol. 2007. PMID: 17408446

5

Human soluble tumor necrosis factor receptor I (sTNF-RI) and interleukin-I receptor antagonist (IL-I Ra) in different stages of acute rheumatic fever.

Kütükçüler N, Karaca NE, Sözeri BY, Koturoğlu G, Kurugöl Z, Ozyürek RA, Aksu G. Kütükçüler N, et al. Among authors: karaca ne. Anadolu Kardiyol Derg. 2008 Apr;8(2):139-42. Anadolu Kardiyol Derg. 2008. PMID: 18400635

6

Increased percentages of autoantibodies in immunoglobulin A-deficient children do not correlate with clinical manifestations.

Gulez N, Karaca NE, Aksu G, Kutukculer N. Gulez N, et al. Among authors: karaca ne. Autoimmunity. 2009 Jan;42(1):74-9. doi: 10.1080/08916930802375711. Autoimmunity. 2009. PMID: 19127458 Free article.

7

Relapsing polychondritis in a child with common variable immunodeficiency.

Karaca NE, Aksu G, Yildiz B, Gulez N, Turk B, Dereli T, Kutukculer N. Karaca NE, et al. Int J Dermatol. 2009 May;48(5):525-8. doi: 10.1111/j.1365-4632.2009.03809.x. Int J Dermatol. 2009. PMID: 19416387

8

Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID.

Karaca NE, Aksu G, Genel F, Gulez N, Can S, Aydinok Y, Aksoylar S, Karaca E, Altuglu I, Kutukculer N. Karaca NE, et al. Among authors: karaca e. Clin Exp Med. 2009 Dec;9(4):339-42. doi: 10.1007/s10238-009-0053-1. Epub 2009 May 21. Clin Exp Med. 2009. PMID: 19458910

9

Clinical and laboratory evaluation of periodically monitored Turkish children with IgG subclass deficiencies.

Karaca NE, Karadeniz C, Aksu G, Kutukculer N. Karaca NE, et al. Asian Pac J Allergy Immunol. 2009 Mar;27(1):43-8. Asian Pac J Allergy Immunol. 2009. PMID: 19548629 Free article.

10

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. 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

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