Prof. Dr. Nesrin Gülez

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

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

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

Journal of Clinical Immunology, 2012

Source : ORCID

HEMOPHAGOCYTIC SYNDROME ASSOCIATED WITH VISCERAL LEISHMANIASIS: REPORT OF TWO CASES

Journal of Clinical Immunology, 2012

Source : ORCID

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) Texte intégral en libre accèsSource : ORCID

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

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

Journal of Clinical Immunology, 2012

Source : ORCID

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

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

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

2012

Source : OpenAlex

Evaluation of Drug Poisoning in Children

Journal of Dr Behcet Uz Children s Hospital, 2011

DOI 10.5222/buchd.2011.105 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

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

Çocuklarda ilaç zehirlenmelerinin değerlendirilmesi

İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2011

Source : OpenAlex

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

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

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

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : OpenAlex

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

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

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

Turkish Journal of Pediatrics, 2010

PMID 20402074 4 citations (OpenAlex) Source : ORCID

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) Texte intégral en libre accèsSource : ORCID

New Laboratory Findings in Turkish Patients with Transient Hypogammaglobulinemia of Infancy

Iranian Journal of Allergy, Asthma and Immunology, 2010

PMID 21131704 23 citations (OpenAlex) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : OpenAlex

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

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

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

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

Archives of Disease in Childhood, 2008

Source : OpenAlex

Delirium induced by topical cyclopentolate use: a case report

Çocuk Sağlığı ve Hastalıkları Dergisi, 2008

Texte intégral en libre accèsSource : OpenAlex

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

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

Clinical & Experimental Immunology, 2008

Source : ORCID

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

Clinical & Experimental Immunology, 2008

Source : ORCID

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

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

Acta Paediatrica, 2008

Source : ORCID

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

Clinical & Experimental Immunology, 2008

Source : ORCID

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

Clinical & Experimental Immunology, 2008

Source : ORCID

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

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

Clinical & Experimental Immunology, 2008

Source : ORCID

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

Clinical & Experimental Immunology, 2008

Source : ORCID

CANDIDA ALBICANS MENINGITIS ASSOCIATED WITH INTRACRANIAL HEMORRHAGE

Marmara Medical Journal, 2007

Source : ORCID

Acute Isoniazid Poisoning Presenting with Status Epilepticus

The Anatolian Journal of General Medical Research, 2006

DOI 10.5222/terh.2006.01729 Texte intégral en libre accèsSource : OpenAlex

Properdin deficiency in a boy with fulminant meningococcal septic shock

Acta Paediatrica, 2006

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

Prognostic Validation of Niclasson Scoring in Patients with Meningococcemia

The Anatolian Journal of General Medical Research, 2006

DOI 10.5222/terh.2006.00268 Texte intégral en libre accèsSource : OpenAlex

Salmonella Meningitis: A Case Report

The Anatolian Journal of General Medical Research, 2005

DOI 10.5222/terh.2005.44788 Texte intégral en libre accèsSource : OpenAlex

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

Ağır kombine immün yetmezlik: olgu sunumu

Meandros Medical And Dental Journal, 2003

Source : OpenAlex