Scientific work

Prof. Dr. Nesrin Gülez

146 publications. The source of the information is stated next to each publication.

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  1. Evaluation of adhesion molecules CD64, CD11b and CD62L in neutrophils and monocytes of peripheral blood for early diagnosis of neonatal infection

    World Journal of Pediatrics, 2012

    DOI 10.1007/s12519-011-0304-6 PMID 21874613 33 citations (Europe PMC) Source: ORCID

  2. Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey

    Clinical Rheumatology, 2012

    DOI 10.1007/s10067-011-1876-1 PMID 22057232 67 citations (OpenAlex) Source: ORCID

  3. CLINICAL FEATURES AND FOLLOW-UP OF TURKISH PATIENTS WITH SYMPTOMATIC HYPOGAMMAGLOBULINEMIA IN INFANCY

    Journal of Clinical Immunology, 2012

    Source: ORCID

  4. HEMOPHAGOCYTIC SYNDROME ASSOCIATED WITH VISCERAL LEISHMANIASIS: REPORT OF TWO CASES

    Journal of Clinical Immunology, 2012

    Source: ORCID

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

    Italian Journal of Pediatrics, 2012

    DOI 10.1186/1824-7288-38-8 PMID 22424479 25 citations (OpenAlex) Open-access full textSource: ORCID

  6. Pesticide-Induced Scleroderma and Early Intensive Immunosuppressive Treatment

    Archives of Environmental & Occupational Health, 2012

    DOI 10.1080/19338244.2011.564231 PMID 22315935 12 citations (OpenAlex) Source: ORCID

  7. THE USE OF INTERFERON-ALPHA TREATMENT IN A PATIENT WITH AUTOSOMAL-RECESSIVE HYPER-IGE SYNDROME (DOCK8 MUTATIONS)

    Journal of Clinical Immunology, 2012

    Source: ORCID

  8. TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) GENE MUTATIONS, CTLA-4 AND ICOS GENE POLYMORPHISMS IN TURKISH PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY

    Journal of Clinical Immunology, 2012

    Source: ORCID

  9. 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

    Journal of Clinical Immunology, 2012

    DOI 10.1007/s10875-012-9717-9 PMID 22699762 31 citations (OpenAlex) Source: ORCID

  10. Evaluation of Growth and Bone Metabolism in Adolescent Patients with Common Variable

    2012

    Source: OpenAlex

  11. Evaluation of Drug Poisoning in Children

    Journal of Dr Behcet Uz Children s Hospital, 2011

    DOI 10.5222/buchd.2011.105 2 citations (OpenAlex) Open-access full textSource: OpenAlex

  12. Comparison of Nebulized Salbutamol, Nebulized Steroid and Systemic Steroid in Acute Bronchiolitis Treatment

    Journal of Dr Behcet Uz Children s Hospital, 2011

    DOI 10.5222/buchd.2011.058 Source: OpenAlex

  13. Çocuklarda ilaç zehirlenmelerinin değerlendirilmesi

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2011

    Source: OpenAlex

  14. Consanguinity Rate and Delay in Diagnosis in Turkish Patients with Combined Immunodeficiencies: a Single-Center Study

    Journal of Clinical Immunology, 2011

    DOI 10.1007/s10875-010-9472-8 PMID 20924659 22 citations (OpenAlex) Source: ORCID

  15. Does OM-85 BV prophylaxis trigger autoimmunity in IgA deficient children?

    International Immunopharmacology, 2011

    DOI 10.1016/j.intimp.2011.06.009 PMID 21771668 15 citations (OpenAlex) Source: ORCID

  16. Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature

    European Journal of Pediatrics, 2011

    DOI 10.1007/s00431-011-1400-2 PMID 21274562 10 citations (OpenAlex) Source: ORCID

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

    Case Reports in Medicine, 2011

    DOI 10.1155/2011/121258 PMID 21541208 7 citations (OpenAlex) Open-access full textSource: ORCID

  18. Immunoglobulin Light Chain Levels Can Be Used to Determine Disease Stage in Children with Juvenile Idiopathic Arthritis

    American Society for Clinical Laboratory Science, 2011

    DOI 10.29074/ascls.24.2.93 PMID 21657141 7 citations (OpenAlex) Open-access full textSource: OpenAlex

  19. Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiency.

    PubMed, 2010

    PMID 20635792 10 citations (OpenAlex) Source: OpenAlex

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

    International Journal of Immunogenetics, 2010

    DOI 10.1111/j.1744-313x.2009.00884.x PMID 19804406 1 citation (OpenAlex) Source: ORCID

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

    Turkish Journal of Pediatrics, 2010

    PMID 20402074 4 citations (OpenAlex) Source: ORCID

  22. Determination of Cut-Off Titers and Agreement Between Immunofluorescence and Immunoblotting Methods for Detecting Antinuclear Antibodies in Children

    Journal of Clinical Laboratory Analysis, 2010

    DOI 10.1002/jcla.20391 PMID 20626019 7 citations (OpenAlex) Open-access full textSource: ORCID

  23. New Laboratory Findings in Turkish Patients with Transient Hypogammaglobulinemia of Infancy

    Iranian Journal of Allergy, Asthma and Immunology, 2010

    PMID 21131704 23 citations (OpenAlex) Open-access full textSource: ORCID

  24. Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

    Journal of Medical Case Reports, 2010

    DOI 10.1186/1752-1947-4-325 PMID 20955551 2 citations (OpenAlex) Open-access full textSource: OpenAlex

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

    Clinical and Experimental Medicine, 2009

    DOI 10.1007/s10238-009-0053-1 PMID 19458910 19 citations (OpenAlex) Source: OpenAlex

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

    Autoimmunity, 2009

    DOI 10.1080/08916930802375711 PMID 19127458 12 citations (OpenAlex) Source: ORCID

  27. Relapsing polychondritis in a child with common variable immunodeficiency

    International Journal of Dermatology, 2009

    DOI 10.1111/j.1365-4632.2009.03809.x PMID 19416387 19 citations (OpenAlex) Source: ORCID

  28. EVALUATION OF ADHESION MOLECULES ON PERIPHERAL BLOOD NEUTROPHILS AND MONOCYTES FOR EARLY DIAGNOSIS OF NEONATAL SEPSIS

    Archives of Disease in Childhood, 2008

    Source: OpenAlex

  29. Delirium induced by topical cyclopentolate use: a case report

    Çocuk Sağlığı ve Hastalıkları Dergisi, 2008

    Open-access full textSource: OpenAlex

  30. A mild clinical spectrum of the X-linked lymphoproliferative syndrome in 6-year-old boy: involvement of XIAP/BIRC-4 gene

    Clinical & Experimental Immunology, 2008

    Source: ORCID

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

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  32. Classification of common variable immunodeficiency patients according to clinical and lymphocytic phenotypes

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  33. Clinical and molecular analysis in seven patients with chronic granulomatous disease and BCG-osis and tuberculosis in three of them

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  34. Immunoglobulin light chain levels have good correlation with classical acute phase reactants in chronic inflammatory disorders

    Acta Paediatrica, 2008

    Source: ORCID

  35. Increased percentages of autoantibodies in immunoglobulin a deficient children may not show any clinical significance

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  36. Patients with CSR defect (without CD40L, CD40, AID and UNG defect) may recover spontaneously during late childhood

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  37. The outcome of patients with unclassified hypogammaglobulinemia in early childhood

    Clinical & Experimental Immunology, 2008

    DOI 10.1111/j.1399-3038.2008.00845.x PMID 19196447 46 citations (OpenAlex) Source: ORCID

  38. Transient hypogammaglobulinemia of infancy and early childhood: outcome of 60 cases

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  39. Two siblings with common variable immunodeficiency: a familial inheritance and remarkable autoimmune manifestations (relapsing polychondritis)

    Clinical & Experimental Immunology, 2008

    Source: ORCID

  40. CANDIDA ALBICANS MENINGITIS ASSOCIATED WITH INTRACRANIAL HEMORRHAGE

    Marmara Medical Journal, 2007

    Source: ORCID

  41. Acute Isoniazid Poisoning Presenting with Status Epilepticus

    The Anatolian Journal of General Medical Research, 2006

    DOI 10.5222/terh.2006.01729 Open-access full textSource: OpenAlex

  42. Properdin deficiency in a boy with fulminant meningococcal septic shock

    Acta Paediatrica, 2006

    DOI 10.1080/08035250600603008 PMID 17062484 13 citations (OpenAlex) Source: OpenAlex

  43. Prognostic Validation of Niclasson Scoring in Patients with Meningococcemia

    The Anatolian Journal of General Medical Research, 2006

    DOI 10.5222/terh.2006.00268 Open-access full textSource: OpenAlex

  44. Salmonella Meningitis: A Case Report

    The Anatolian Journal of General Medical Research, 2005

    DOI 10.5222/terh.2005.44788 Open-access full textSource: OpenAlex

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

    Annals of Tropical Paediatrics, 2004

    DOI 10.1179/027249304225019019 PMID 15479578 4 citations (OpenAlex) Source: OpenAlex

  46. Ağır kombine immün yetmezlik: olgu sunumu

    Meandros Medical And Dental Journal, 2003

    Source: OpenAlex