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Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

Journal of clinical immunology, 2020-04, Vol.40 (3), p.494-502

2020

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A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly

Journal of pediatric hematology/oncology, 2018-04, Vol.40 (3), p.248-251

2018

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False Negative Next-Generation-Sequencing Analysis in a Lipopolysa ccharide-Responsive Beige-Like Anchor Defect

Turkish Archives of Pediatrics, 2024-03, Vol.59 (2), p.221-223

2024

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ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia

Turkish journal of pediatrics, 2023-07, Vol.65 (4), p.698-703

2023

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Nutritional status of children with primary immunodeficiency: A single center experience

Pediatric investigation, 2022-01, Vol.64 (1), p.e14996-n/a

2022

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Maternofetal Transfusion, Maternal Chimerism, and Maternal Engraftment: A Mystery in Health and Disease

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2021-11, Vol.9 (11), p.4154-4155

Cagdas, Deniz

2021

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A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

Journal of clinical immunology, 2014-11, Vol.34 (8), p.1009-1014

2014

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DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection

Turkish journal of pediatrics, 2023-05, Vol.65 (3), p.536-541

2023

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Impact of mannose‐binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children

Pediatric pulmonology, 2020-05, Vol.55 (5), p.1190-1198

2020

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Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients

European journal of pediatrics, 2012-10, Vol.171 (10), p.1527-1531

2012

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A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Journal of rheumatology, 2020-01, Vol.47 (1), p.117-125

2020

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Isolation, Chemical Composition, Physicochemical Properties, and Antibacterial Activity of Cupressus sempervirens L. Essential Oil

Journal of essential oil-bearing plants (Dehra Dun), 2021-05, Vol.24 (3), p.439-452

2021

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Retroperitoneal Abscess in Severe Combined Immunodeficiency Probably Due to BCG Vaccine

Astım allerji immünoloji, 2020-08, Vol.18 (2), p.98-101

2020

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The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study

Turkish journal of medical sciences, 2022-01, Vol.52 (4), p.1139-1147

2022

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Mutation in BTK Gene Causing an Atypical Presentation of XLA

Astım allerji immünoloji, 2022-12, Vol.20 (3), p.197-201

2022

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APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity

Scandinavian journal of immunology, 2023-08, Vol.98 (2), p.e13299-n/a

2023

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Correction to: Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia

Odontology, 2021-04, Vol.109 (2), p.483-483

2021

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Detection of parasites in children with chronic diarrhea

Pediatrics international, 2016-06, Vol.58 (6), p.531-533

2016

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A Novel Interleukin 17 Receptor A Mutation in a Child with Chronic Mucocutaneous Candidiasis and Staphylococcal Skin Infections

Turkish Archives of Pediatrics, 2023-07

2023

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DiGeorge Syndrome: Simultaneously Diagnosis of A Mother-Baby Pair With Great Clinical Variability

Gazi tıp dergisi, 2022-04, Vol.33 (2), p.179-182

2022

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Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

Scientific reports, 2024-05, Vol.14 (1), p.10052-12, Article 10052

2024

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A Rare Central Nervous System Involvement Due to CTLA-4 Gene Defect

Noro-Psikiyatri Arsivi, 2022-09, Vol.59 (3), p.248-252

2022

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D-dimer elevation during tranexamic acid therapy and the debate on the therapeutic approach in hereditary angioedema type I

Alergologia Polska - Polish Journal of Allergology, 2023, Vol.10 (1), p.63-67

2023

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Two SCID cases with Cernunnos‐XLF deficiency successfully treated by hematopoietic stem cell transplantation

Pediatric transplantation, 2012-08, Vol.16 (5), p.E167-E171

2012

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Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion

Pediatric allergy and immunology, 2014-12, Vol.25 (8), p.817-819

2014

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Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly

False Negative Next-Generation-Sequencing Analysis in a Lipopolysa ccharide-Responsive Beige-Like Anchor Defect

ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia

Nutritional status of children with primary immunodeficiency: A single center experience

Maternofetal Transfusion, Maternal Chimerism, and Maternal Engraftment: A Mystery in Health and Disease

A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection

Impact of mannose‐binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Isolation, Chemical Composition, Physicochemical Properties, and Antibacterial Activity of Cupressus sempervirens L. Essential Oil

Retroperitoneal Abscess in Severe Combined Immunodeficiency Probably Due to BCG Vaccine

The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study

Mutation in BTK Gene Causing an Atypical Presentation of XLA

APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity

Correction to: Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia

Detection of parasites in children with chronic diarrhea

A Novel Interleukin 17 Receptor A Mutation in a Child with Chronic Mucocutaneous Candidiasis and Staphylococcal Skin Infections

DiGeorge Syndrome: Simultaneously Diagnosis of A Mother-Baby Pair With Great Clinical Variability

Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

A Rare Central Nervous System Involvement Due to CTLA-4 Gene Defect

D-dimer elevation during tranexamic acid therapy and the debate on the therapeutic approach in hereditary angioedema type I

Two SCID cases with Cernunnos‐XLF deficiency successfully treated by hematopoietic stem cell transplantation

Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion

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