Gulez N - Search Results

1

22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management.

Ozen S, Akcal O, Taskirdi I, Haci IA, Karaca NE, Gulez N, Aksu G, Genel F, Kutukculer N. Ozen S, et al. Among authors: gulez n. Allergol Immunopathol (Madr). 2021 Jan 2;49(1):95-100. doi: 10.15586/aei.v49i1.24. eCollection 2021. Allergol Immunopathol (Madr). 2021. PMID: 33528935

2

Fulminant amoebiasis in a child with recurrent multiple amoebic liver abscesses and pleuropulmonary complications.

Genel F, Atlihan F, Targan S, Gulez N, Hacikara S, Karaca I. Genel F, et al. Among authors: gulez n. Ann Trop Paediatr. 2004 Sep;24(3):267-9. doi: 10.1179/027249304225019019. Ann Trop Paediatr. 2004. PMID: 15479578

3

Properdin deficiency in a boy with fulminant meningococcal septic shock.

Genel F, Atlihan F, Gulez N, Sjöholm AG, Skattum L, Truedsson L. Genel F, et al. Among authors: gulez n. Acta Paediatr. 2006 Nov;95(11):1498-1500. doi: 10.1080/08035250600603008. Acta Paediatr. 2006. PMID: 17062484

4

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. Autoimmunity. 2009 Jan;42(1):74-9. doi: 10.1080/08916930802375711. Autoimmunity. 2009. PMID: 19127458 Free article.

5

The outcome of patients with unclassified hypogammaglobulinemia in early childhood.

Kutukculer N, Gulez N. Kutukculer N, et al. Among authors: gulez n. Pediatr Allergy Immunol. 2009 Nov;20(7):693-8. doi: 10.1111/j.1399-3038.2008.00845.x. Epub 2009 Jan 31. Pediatr Allergy Immunol. 2009. PMID: 19196447

6

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. Among authors: gulez n. Int J Dermatol. 2009 May;48(5):525-8. doi: 10.1111/j.1365-4632.2009.03809.x. Int J Dermatol. 2009. PMID: 19416387

7

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: gulez n. 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

8

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: gulez n. 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

9

Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings.

Edeer-Karaca N, Gülez N, Aksu G, Kütükcüler N. Edeer-Karaca N, et al. Among authors: gulez n. Turk J Pediatr. 2010 Jan-Feb;52(1):89-93. Turk J Pediatr. 2010. PMID: 20402074

10

Determination of cut-off titers and agreement between immunofluorescence and immunoblotting methods for detecting antinuclear antibodies in children.

Aksu G, Gulez N, Azarsiz E, Karaca N, Kutukçuler N. Aksu G, et al. Among authors: gulez n. J Clin Lab Anal. 2010;24(4):230-6. doi: 10.1002/jcla.20391. J Clin Lab Anal. 2010. PMID: 20626019 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

61 results

Search Page

Filters