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List of works by Safa Bariş

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

scientific article published on 10 October 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

scientific article published on 14 September 2020

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

scientific article

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.

scientific article published on January 2011

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

scientific article published in September 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

scientific article published on 6 April 2017

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

scientific article

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

scientific article published on 01 August 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.

scientific article published on 23 September 2008

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

scientific article published on 27 September 2017

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

scientific article

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.

scientific article published on 16 March 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

scientific article published on 07 November 2018

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

scientific article published on 7 June 2017

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

scientific article published on 27 January 2017

Experience with intravenous immunoglobulin in severe childhood atopic dermatitis

scientific article published on 19 August 2011

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

scientific article

Granzyme B gene polymorphism associated with subacute sclerosing panencephalitis

scientific article published on 29 May 2014

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

scientific article published on 10 March 2017

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

scientific article published on 13 December 2018

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

scientific article published on 12 December 2016

ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

scientific article published on 09 October 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.

scientific article published on 11 December 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

scientific article published on 14 July 2015

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

scientific article

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

scientific article published on 06 October 2020

Osteoporosis: an ignored complication of CVID

scientific article published on 06 June 2011

Outcome of hypogammaglobulinemia in children: immunoglobulin levels as predictors

scientific article published on 19 September 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.

scientific article

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

scientific article published on 04 October 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.

scientific article

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

scientific article published on 10 September 2015

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

scientific article published on 17 June 2015

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

scientific article

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

scientific article

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

scientific article published on 08 April 2021

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

scientific article published on 19 September 2017

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

scientific article published on 14 February 2020

Treatment of pediatric Burkitt lymphoma in Turkey.

scientific article published on October 2010

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

scientific article published on 4 November 2013