Bilimsel çalışmalar
Prof. Dr. Safa Barış
395 yayın. Her yayının yanında bilginin kaynağı yazar.
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A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells
Journal of Clinical Immunology, 2021
DOI 10.1007/s10875-020-00889-1 PMID 33040278 5 atıf (Europe PMC) Kaynak: ORCID
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Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation
Journal of clinical immunology, 2021
DOI 10.1007/s10875-020-00943-y PMID 33475942 43 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC
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Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis
Journal of clinical immunology, 2021
DOI 10.1007/s10875-020-00878-4 PMID 33025377 11 atıf (Europe PMC) Kaynak: Europe PMC
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Primary Immun Deficiency in Patients with Non-Cystic Fibrosis Bronchiectasis and Its Relationship with Clinical Parameters
Turkish thoracic journal, 2021
DOI 10.5152/turkthoracj.2020.19077 PMID 33646102 6 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC
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Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimicking ATM-mutated patients
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2021
DOI 10.1111/pai.13387 PMID 33012025 7 atıf (Europe PMC) Kaynak: Europe PMC
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Reference values for T and B lymphocyte subpopulations in Turkish children and adults
Turkish journal of medical sciences, 2021
DOI 10.3906/sag-2010-176 PMID 33754649 39 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC
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Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency
Journal of Clinical Immunology, 2021
DOI 10.1007/s10875-021-01031-5 PMID 33929673 40 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Prevalence of allergic disorders and risk factors associated with food allergy in Turkish preschoolers
Allergologia et Immunopathologia, 2021
DOI 10.15586/aei.v49i1.23 PMID 33528924 22 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Homozygous IL37 mutation associated with infantile inflammatory bowel disease
Proceedings of the National Academy of Sciences, 2021
DOI 10.1073/pnas.2009217118 PMID 33674380 27 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Two patients with chronic mucocutaneous candidiasis caused by TRAF3IP2 deficiency
Journal of Allergy and Clinical Immunology, 2021
DOI 10.1016/j.jaci.2020.12.629 PMID 33359359 16 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency
Journal of Clinical Immunology, 2021
DOI 10.1007/s10875-021-01042-2 PMID 33950325 9 atıf (OpenAlex) Kaynak: OpenAlex
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Immune alterations in subacute sclerosing panencephalitis reflect an incompetent response to eliminate the measles virus
PLoS ONE, 2021
DOI 10.1371/journal.pone.0245077 PMID 33411786 8 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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A Novel ATM Gene Mutation Affecting Splicing in an Ataxia-Telangiectasia Patient
Molecular Syndromology, 2021
DOI 10.1159/000518629 PMID 35221880 2 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Primary antibody deficiencies in Turkey: molecular and clinical aspects
Immunologic Research, 2021
DOI 10.1007/s12026-021-09242-z PMID 34618307 4 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Human immunodeficiency reveals GIMAP5 as lymphocyte-specific regulator of senescence
bioRxiv (Cold Spring Harbor Laboratory), 2021
DOI 10.1101/2021.02.22.432146 6 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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IL-10R Eksikliği ve Lenfoma
2021
Kaynak: OpenAlex
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The evaluation of radiosensitivity in patients with STAT3 deficiency
2021
Kaynak: OpenAlex
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Primer İmmün Yetmezliklerdeİmmünoglobulin Replasman Tedavisi:Güncel Durum Raporu 2019
2020
Kaynak: OpenAlex
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Hematopoietic stem cell transplantation in CD40 ligand deficiency: A single‐center experience
Pediatric Transplantation, 2020
DOI 10.1111/petr.13768 PMID 32573870 Kaynak: OpenAlex
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A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis
Clinical Immunology, 2020
DOI 10.1016/j.clim.2020.108645 PMID 33301882 23 atıf (OpenAlex) Kaynak: OpenAlex
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Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty
Hormone Research in Paediatrics, 2020
DOI 10.1159/000505329 PMID 31972562 8 atıf (Europe PMC) Kaynak: ORCID
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A regulatory T cell Notch4–GDF15 axis licenses tissue inflammation in asthma
Nature Immunology, 2020
DOI 10.1038/s41590-020-0777-3 PMID 32929274 116 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study
Pediatric Allergy and Immunology, 2020
DOI 10.1111/pai.13231 PMID 32060950 16 atıf (Europe PMC) Kaynak: ORCID
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Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype
Clinical Immunology, 2020
DOI 10.1016/j.clim.2019.108295 PMID 31683053 Açık erişimli tam metinKaynak: ORCID
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Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
Journal of Allergy and Clinical Immunology, 2020
DOI 10.1016/j.jaci.2020.09.010 PMID 32980424 340 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
Journal of Allergy and Clinical Immunology, 2020
DOI 10.1016/j.jaci.2019.11.051 PMID 32278790 143 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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All together to Fight COVID-19
American Journal of Tropical Medicine and Hygiene, 2020
DOI 10.4269/ajtmh.20-0281 PMID 32323644 107 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency
Blood, 2020
DOI 10.1182/blood.2020006738 PMID 32603431 103 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency
International Archives of Allergy and Immunology, 2020
DOI 10.1159/000504598 PMID 31901904 23 atıf (OpenAlex) Kaynak: OpenAlex
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Mutational landscape of severe combined immunodeficiency patients from Turkey
International Journal of Immunogenetics, 2020
DOI 10.1111/iji.12496 PMID 32445296 22 atıf (OpenAlex) Kaynak: OpenAlex
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Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort
The Journal of Allergy and Clinical Immunology In Practice, 2020
DOI 10.1016/j.jaip.2020.07.030 PMID 32736065 19 atıf (OpenAlex) Kaynak: OpenAlex
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Immediate adverse reactions to intravenous immunoglobulin in primary immune deficiencies: a single center experience
The Turkish Journal of Pediatrics, 2020
DOI 10.24953/turkjped.2020.03.004 PMID 32558411 9 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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U100: An Innovative USERN Platform for Education and Research Without Borders
ACTA MEDICA IRANICA, 2020
DOI 10.18502/acta.v58i1.3698 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Lentiviral vector-based SARS-CoV-2 pseudovirus enables analysis of neutralizing activity in COVID-19 convalescent plasma
bioRxiv (Cold Spring Harbor Laboratory), 2020
DOI 10.1101/2020.12.28.424590 Açık erişimli tam metinKaynak: OpenAlex
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SKIG kullanım ilkeleri nelerdir? SKIG dozu ve sıklığı nasıl belirlenmelidir?
2019
Kaynak: OpenAlex
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Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency
Journal of Allergy and Clinical Immunology: In Practice, 2019
DOI 10.1016/j.jaip.2019.06.011 PMID 31238161 127 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency
Journal of Clinical Immunology, 2019
DOI 10.1007/s10875-019-00615-6 PMID 30903456 12 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty
Dspace Repository (Marmara Üniversitesi), 2019
Açık erişimli tam metinKaynak: OpenAlex
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Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat
Pediatric Blood & Cancer, 2019
DOI 10.1002/pbc.28091 PMID 31736244 19 atıf (OpenAlex) Kaynak: OpenAlex
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Basic Immunology-Humoral
TURKISH JOURNAL OF HEMATOLOGY, 2019
Kaynak: ORCID
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Basic immunology-humoral
Turkish Journal of Hematology, 2019
Kaynak: ORCID
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Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies
International archives of allergy and immunology, 2019
DOI 10.1159/000492824 PMID 30404088 4 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation
Journal of clinical immunology, 2019
DOI 10.1007/s10875-018-0575-y PMID 30543054 37 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients
Allergy: European Journal of Allergy and Clinical Immunology, 2019
DOI 10.1111/all.14081 PMID 31596517 18 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Immune system defects in DiGeorge syndrome and association with clinical course
Scandinavian journal of immunology, 2019
DOI 10.1111/sji.12809 PMID 31322747 10 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Lymphocyte functions in patients with chronic granulomatous disease and carrier individuals,Kronik granülomatöz hastalarında ve bu hastalığı genetik olarak taşıyan bireylerde lenfosit fonksiyonları
Turkish Journal of Immunology, 2019
DOI 10.25002/tji.2019.1111 Açık erişimli tam metinKaynak: ORCID
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MMR immunisation practices in children with a history of egg allergy
ALLERGY, 2019
Kaynak: ORCID
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Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency
Journal of Allergy and Clinical Immunology: In Practice, 2019
DOI 10.1016/j.jaip.2019.02.038 PMID 30877075 66 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Outcomes and treatment strategies for autoimmunity and hyperinflammation in patients with RAG deficiency
The Journal of Allergy and Clinical Immunology: In Practice, 2019
Kaynak: ORCID
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Polymerase $δ$ deficiency causes syndromic immunodeficiency with replicative stress
The Journal of clinical investigation, 2019
DOI 10.1172/jci128903 PMID 31449058 41 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID