Lista de obras -

A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

scientific article published on 01 February 2019

A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

artículo científico publicado en 2020

A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

scientific article published on 01 June 2018

A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma

artículo científico publicado en 2020

A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients

artículo científico publicado en 2017

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

scientific article published on 22 June 2019

Acquired origin of the left anterior descending coronary artery from the pulmonary artery: A complication of the arterial switch operation. ⬇️

artículo científico publicado en 2011

Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma.

artículo científico publicado en 2009

Author Correction: A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma

scientific article published on 19 November 2020

Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype

scientific article published on 01 November 2019

Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis

artículo científico publicado en 2017

Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation

artículo científico publicado en 2014

Clinical variability of asphyxiating thoracic dystrophy (Jeune) syndrome: Evaluation and classification of 13 patients

artículo científico publicado en 2009

Coronary events and anatomy after arterial switch operation for transposition of the great arteries: detection by 16-row multislice computed tomography angiography in pediatric patients.

artículo científico publicado en 2008

Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

artículo científico publicado en 2017

DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

artículo científico publicado en 2012

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

artículo científico publicado en 2018

Duration and dispersion of the P wave after the Senning operation

scientific article published on 27 October 2009

Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

artículo científico publicado en 2018

Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation.

artículo científico publicado en 2017

Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.

artículo científico publicado en 2017

Experience with intravenous immunoglobulin in severe childhood atopic dermatitis

artículo científico publicado en 2011

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

artículo científico publicado en 2015

Granzyme B gene polymorphism associated with subacute sclerosing panencephalitis

artículo científico publicado en 2014

Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide

artículo científico publicado en 2017

Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.

artículo científico publicado en 2018

IL-12Rβ1 defect presenting with massive intraabdominal lymphadenopathy due to Mycobacterium intracellulare: A case report.

artículo científico publicado en 2016

ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

artículo científico publicado en 2019

Immune system defects in DiGeorge syndrome and association with clinical course

scientific article published on 09 September 2019

Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study.

artículo científico publicado en 2017

Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

scientific article published on 17 November 2019

Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study.

artículo científico publicado en 2015

Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.

artículo científico publicado en 2016

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

artículo científico publicado en 2020

Osteoporosis: an ignored complication of CVID

artículo científico publicado en 2011

Outcome of hypogammaglobulinemia in children: immunoglobulin levels as predictors

artículo científico publicado en 2010

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

scientific article published on 12 March 2019

Papaverine chloride as a topical vasodilator in accidental injection of adrenaline into a digital finger.

artículo científico publicado en 2011

Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimicking ATM mutated patients

artículo científico publicado en 2020

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress

scientific article published on 01 October 2019

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.

artículo científico publicado en 2015

Predictive risk factors for relapse after cessation of inhaled corticosteroids in well-controlled childhood asthma

artículo científico publicado en 2015

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population.

artículo científico publicado en 2015

Serum immunoglobulin levels as a predictive factor for a better outcome of non-atopic childhood asthma.

artículo científico publicado en 2010

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

artículo científico publicado en 2016

Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4<sup>+</sup> T cell perturbations

artículo científico publicado en 2021

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

artículo científico publicado en 2017

The evaluation of malignancies in Turkish primary immunotherapy patients; a multicenter study

artículo científico publicado en 2020

Treatment of pediatric Burkitt lymphoma in Turkey.

artículo científico publicado en 2010

Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.

artículo científico publicado en 2013

Lista de obras de

A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma

A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

Acquired origin of the left anterior descending coronary artery from the pulmonary artery: A complication of the arterial switch operation. ⬇️

Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma.

Author Correction: A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma

Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype

Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis

Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation

Clinical variability of asphyxiating thoracic dystrophy (Jeune) syndrome: Evaluation and classification of 13 patients

Coronary events and anatomy after arterial switch operation for transposition of the great arteries: detection by 16-row multislice computed tomography angiography in pediatric patients.

Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

Duration and dispersion of the P wave after the Senning operation

Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation.

Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.

Experience with intravenous immunoglobulin in severe childhood atopic dermatitis

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

Granzyme B gene polymorphism associated with subacute sclerosing panencephalitis

Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide

Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.

IL-12Rβ1 defect presenting with massive intraabdominal lymphadenopathy due to Mycobacterium intracellulare: A case report.

ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

Immune system defects in DiGeorge syndrome and association with clinical course

Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study.

Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study.

Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

Osteoporosis: an ignored complication of CVID

Outcome of hypogammaglobulinemia in children: immunoglobulin levels as predictors

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

Papaverine chloride as a topical vasodilator in accidental injection of adrenaline into a digital finger.

Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimicking ATM mutated patients

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.

Predictive risk factors for relapse after cessation of inhaled corticosteroids in well-controlled childhood asthma

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population.

Serum immunoglobulin levels as a predictive factor for a better outcome of non-atopic childhood asthma.

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4<sup>+</sup> T cell perturbations

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

The evaluation of malignancies in Turkish primary immunotherapy patients; a multicenter study

Treatment of pediatric Burkitt lymphoma in Turkey.

Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.