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A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease

Clinical immunology (Orlando, Fla.), 2015-07, Vol.159 (1), p.58-62

2015

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The Frequency of HLA-A, HLA-B, and HLA-DRB1 Alleles in Patients with Acute Lymphoblastic Leukemia in the Turkish Population: A Case-Control Study

Turkish journal of haematology, 2016-12, Vol.33 (4), p.339-345

2016

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Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis

Haematologica (Roma), 2016-10, Vol.101 (10), p.1180-1189

2016

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THE INFLUENCE OF HLA-DQ2 HETERODIMERS ON THE CLINICAL FEATURES AND LABORATORY OF PATIENTS WITH CELIAC DISEASE

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2015-12, Vol.32 (6), p.2594-2599

2015

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Clericuzio-type Poikiloderma with Neutropenia Syndrome in a Turkish Family: a Three Report of Siblings with Mutation in the C16orf57 gene

Iranian journal of allergy, asthma, and immunology, 2015-06, Vol.14 (3), p.331-331

2015

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Silent brain infarcts in two patients with zeta chain-associated protein 70 kDa (ZAP70) deficiency

Clinical immunology (Orlando, Fla.), 2015-05, Vol.158 (1), p.88-91

2015

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Silent brain infarcts in two patients with zeta chain-associated protein 70kDa (ZAP70) deficiency

Clinical immunology (Orlando, Fla.), 2015-05, Vol.158 (1), p.88-91

2015

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AMINO ACID LEVELS IN CHILDREN WITH CELIAC DISEASE

Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral, 2015-07, Vol.32 (1), p.139-143

2015

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Effect of early atopic sensitization in children aged 0–2 years on the development of asthma symptoms at 9–11 years of age

World journal of pediatrics : WJP, 2022-11, Vol.18 (11), p.753-760

2022

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Increased lipoxin B4 levels in children with atopic dermatitis

Paediatrica Indonesiana, 2019-10, Vol.59 (5), p.271-5

2019

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The association of forced expiratory volume in one second and forced expiratory flow at 50% of the vital capacity, peak expiratory flow parameters, and blood eosinophil counts in exercise-induced bronchospasm in children with mild asthma

Asia Pacific allergy, 2015-04, Vol.5 (2), p.98-102

2015

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Hair dyes and temporary tattoos are a real hazard for adolescents?

European annals of allergy and clinical immunology, 2014-01, Vol.46 (1), p.35

2014

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Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases: A Single-Center Experience

Experimental and clinical transplantation, 2017-06, Vol.15 (3), p.337-343

2017

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Grass pollen triggered anaphylaxis in an adolescent boy

European annals of allergy and clinical immunology, 2015-01, Vol.47 (1), p.20

2015

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Contribution of KIR genes, HLA class I ligands, and KIR/HLA class I ligand combinations on the genetic predisposition to celiac disease and coexisting celiac disease and type 1 diabetes mellitus

Revista española de enfermedades digestivas, 2015-09, Vol.107 (9), p.547-553

2015

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XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination

Blood, 2016-08, Vol.128 (5), p.650-659

2016

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A case of hereditary angioedema who presented with difficulty in urination and globe

European annals of allergy and clinical immunology, 2014-01, Vol.46 (1), p.60

2014

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X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report

European journal of microbiology & immunology, 2014-09, Vol.4 (3), p.174-176

2014

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A case of XLF deficiency presented with diffuse large B cell lymphoma in the brain

Clinical immunology (Orlando, Fla.), 2015-12, Vol.161 (2), p.394-395

2015

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Plasma glutamine and cystine are decreased and negatively correlated with endomysial antibody in children with celiac disease

Asia Pacific journal of clinical nutrition, 2016-01, Vol.25 (3), p.452-456

2016

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Atypical Severe Combined Immunodeficiency Caused by a Novel Homozygous Mutation In Rag1 Gene in a Girl who Presented with Pyoderma Gangrenosum: A Case Report and Literature Review

Journal of clinical immunology, 2014-10, Vol.34 (7), p.792-795

2014

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Relationships of Human Leukocyte Antigen-A, -B, -DRB1 Alleles, and Haplotypes in 129 Ethnic Turkish Patients With Acute Myeloblastic Leukemia

Laboratory medicine, 2015-08, Vol.46 (3), p.195-199

2015

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The Role of Irisin, Insulin and Leptin in Maternal and Fetal Interaction

Journal of clinical research in pediatric endocrinology, 2018-12, Vol.10 (4), p.307-315

2018

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Combined immunodeficiencies: twenty years experience from a single center in Turkey

Central-European journal of immunology, 2016, Vol.41 (1), p.107-115

2016

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A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease

The Frequency of HLA-A, HLA-B, and HLA-DRB1 Alleles in Patients with Acute Lymphoblastic Leukemia in the Turkish Population: A Case-Control Study

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis

THE INFLUENCE OF HLA-DQ2 HETERODIMERS ON THE CLINICAL FEATURES AND LABORATORY OF PATIENTS WITH CELIAC DISEASE

Clericuzio-type Poikiloderma with Neutropenia Syndrome in a Turkish Family: a Three Report of Siblings with Mutation in the C16orf57 gene

Silent brain infarcts in two patients with zeta chain-associated protein 70 kDa (ZAP70) deficiency

Silent brain infarcts in two patients with zeta chain-associated protein 70kDa (ZAP70) deficiency

AMINO ACID LEVELS IN CHILDREN WITH CELIAC DISEASE

Effect of early atopic sensitization in children aged 0–2 years on the development of asthma symptoms at 9–11 years of age

Increased lipoxin B4 levels in children with atopic dermatitis

The association of forced expiratory volume in one second and forced expiratory flow at 50% of the vital capacity, peak expiratory flow parameters, and blood eosinophil counts in exercise-induced bronchospasm in children with mild asthma

Hair dyes and temporary tattoos are a real hazard for adolescents?

Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases: A Single-Center Experience

Grass pollen triggered anaphylaxis in an adolescent boy

Contribution of KIR genes, HLA class I ligands, and KIR/HLA class I ligand combinations on the genetic predisposition to celiac disease and coexisting celiac disease and type 1 diabetes mellitus

EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children

XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination

A case of hereditary angioedema who presented with difficulty in urination and globe

X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report

A case of XLF deficiency presented with diffuse large B cell lymphoma in the brain

Plasma glutamine and cystine are decreased and negatively correlated with endomysial antibody in children with celiac disease

Atypical Severe Combined Immunodeficiency Caused by a Novel Homozygous Mutation In Rag1 Gene in a Girl who Presented with Pyoderma Gangrenosum: A Case Report and Literature Review

Relationships of Human Leukocyte Antigen-A, -B, -DRB1 Alleles, and Haplotypes in 129 Ethnic Turkish Patients With Acute Myeloblastic Leukemia

The Role of Irisin, Insulin and Leptin in Maternal and Fetal Interaction

Combined immunodeficiencies: twenty years experience from a single center in Turkey

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