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Combined immunodeficiencies: twenty years experience from a single center in Turkey.
- Published in:
- Central European Journal of Immunology, 2016, v. 41, n. 1, p. 107, doi. 10.5114/ceji.2015.56168
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- Article
A Girl with Autoimmune Cytopenias, Nonmalignant Lymphadenopathy, and Recurrent Infections.
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- Case Reports in Immunology, 2012, p. 1, doi. 10.1155/2012/196417
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- Publication type:
- Article
Educational paper: primary antibody deficiencies.
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- 2011
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- Publication type:
- journal article
Educational paper. The expanding clinical and immunological spectrum of severe combined immunodeficiency.
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- 2011
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- Publication type:
- journal article
Late-onset adenosine deaminase deficiency presenting with Heck's disease.
- Published in:
- 2010
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- Publication type:
- journal article
Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency.
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- European Journal of Pediatrics, 2009, v. 168, n. 1, p. 87, doi. 10.1007/s00431-008-0718-x
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- Publication type:
- Article
Epigenetic Immune Cell Counting to Analyze Potential Biomarkers in Preterm Infants: A Proof of Principle in Necrotizing Enterocolitis.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2372, doi. 10.3390/ijms24032372
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- Article
Regulatory T Cells in Development and Prediction of Necrotizing Enterocolitis in Preterm Neonates: A Scoping Review.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810903
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- Publication type:
- Article
CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.
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- Journal of Clinical Investigation, 2010, v. 120, n. 4, p. 1265, doi. 10.1172/JCI39748
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- Article
A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.
- Published in:
- 2009
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- Publication type:
- journal article
A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.
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- 2006
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- Publication type:
- journal article
Diagnosing mycobacterial lymphadenitis in children using fine needle aspiration biopsy: Cytomorphology, ZN staining and autofluorescence-Making more of less.
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- Diagnostic Cytopathology, 2008, v. 36, n. 4, p. 245, doi. 10.1002/dc.20788
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- Publication type:
- Article
Case report: Severe combined immunodeficiency with ligase 1 deficiency and Omenn-like manifestation.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1033338
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- Publication type:
- Article
Deciphering imprints of impaired memory B-cell maturation in germinal centers of three patients with common variable immunodeficiency.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.959002
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- Publication type:
- Article
The Euroflow PID Orientation Tube in the diagnostic workup of primary immunodeficiency: Daily practice performance in a tertiary university hospital.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.937738
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- Publication type:
- Article
CD45RB Glycosylation and Ig Isotype Define Maturation of Functionally Distinct B Cell Subsets in Human Peripheral Blood.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.891316
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- Publication type:
- Article
Diagnostic Value of a Protocolized In-Depth Evaluation of Pediatric Bone Marrow Failure: A Multi-Center Prospective Cohort Study.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.883826
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- Publication type:
- Article
Functional and Immune Modulatory Characteristics of Bone Marrow Mesenchymal Stromal Cells in Patients With Aplastic Anemia: A Systematic Review.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.859668
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- Publication type:
- Article
AKT Hyperphosphorylation and T Cell Exhaustion in Down Syndrome.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.724436
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- Article
Editorial: New Insights Into B Cell Subsets in Health and Disease.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.854889
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- Publication type:
- Article
Optimizing diagnostic methods and stem cell transplantation outcomes in pediatric bone marrow failure: a 50-year single center experience.
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- European Journal of Pediatrics, 2023, v. 182, n. 9, p. 4195, doi. 10.1007/s00431-023-05093-y
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- Publication type:
- Article
Cost-effectiveness of newborn screening for severe combined immunodeficiency.
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- 2019
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- Publication type:
- journal article
Overview of 15-year severe combined immunodeficiency in the Netherlands: towards newborn blood spot screening.
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- 2015
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- Publication type:
- journal article
ImmunoGlobulin galaxy (IGGalaxy) for simple determination and quantitation of immunoglobulin heavy chain rearrangements from NGS.
- Published in:
- BMC Immunology, 2014, v. 15, n. 1, p. 44, doi. 10.1186/s12865-014-0059-7
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- Publication type:
- Article
Checkpoints of B cell differentiation: visualizing Ig-centric processes.
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- Annals of the New York Academy of Sciences, 2011, v. 1246, n. 1, p. 11, doi. 10.1111/j.1749-6632.2011.06278.x
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- Article
Disturbed B-lymphocytes selection in autoimmune lymphoproliferative syndrome.
- Published in:
- 2015
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- Publication type:
- Abstract
Decreased IL7Rα and TdT expression underlie the skewed immunoglobulin repertoire of human B-cell precursors from fetal origin.
- Published in:
- Scientific Reports, 2016, p. 33924, doi. 10.1038/srep33924
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- Publication type:
- Article
Identification of CVID Patients With Defects in Immune Repertoire Formation or Specification.
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- Frontiers in Immunology, 2018, p. N.PAG, doi. 10.3389/fimmu.2018.02545
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- Publication type:
- Article
Exhaustion of the CD8<sup>+</sup> T Cell Compartment in Patients with Mutations in Phosphoinositide 3-Kinase Delta.
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- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00446
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- Publication type:
- Article
Public clonotypes and convergent recombination characterize the naïve cD8+ T-cell receptor repertoire of extremely Preterm neonates.
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- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01859
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- Publication type:
- Article
Immune Dysfunction in Children with CHARGE Syndrome: A Cross-Sectional Study.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0142350
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- Article
Pediatric Bone Marrow Failure: A Broad Landscape in Need of Personalized Management.
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- Journal of Clinical Medicine, 2023, v. 12, n. 22, p. 7185, doi. 10.3390/jcm12227185
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- Publication type:
- Article
Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation.
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- Pediatric Transplantation, 2012, v. 16, n. 5, p. E167, doi. 10.1111/j.1399-3046.2011.01491.x
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- Publication type:
- Article
Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency.
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- Frontiers in Immunology, 2020, p. 1, doi. 10.3389/fimmu.2020.00614
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- Publication type:
- Article
Delineating Human B Cell Precursor Development With Genetically Identified PID Cases as a Model.
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- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02680
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- Article
Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents' Perspective on Ataxia Telangiectasia.
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- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02438
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- Publication type:
- Article
Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in Humans.
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- Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.01913
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- Publication type:
- Article
EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.01271
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- Publication type:
- Article
Impaired CpG Demethylation in Common Variable Immunodeficiency Associates With B Cell Phenotype and Proliferation Rate.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00878
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- Publication type:
- Article
The EuroFlow PID Orientation Tube for Flow Cytometric Diagnostic Screening of Primary Immunodeficiencies of the Lymphoid System.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00246
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- Publication type:
- Article
The defect in humoral immunity in patients with Nijmegen breakage syndrome is explained by defects in peripheral B lymphocyte maturation.
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- Cytometry. Part A, 2012, v. 81A, n. 10, p. 835, doi. 10.1002/cyto.a.22108
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- Publication type:
- Article
Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects.
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- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1219, doi. 10.1038/ejhg.2013.40
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- Publication type:
- Article
The presence of CLL-associated stereotypic B cell receptors in the normal BCR repertoire from healthy individuals increases with age.
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- Immunity & Ageing, 2019, v. 16, n. 1, p. N.PAG, doi. 10.1186/s12979-019-0163-x
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- Publication type:
- Article
Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.
- Published in:
- 2019
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- Publication type:
- journal article
Decreased somatic hypermutation induces an impaired peripheral B cell tolerance checkpoint.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Normal Numbers of Stem Cell Memory T Cells Despite Strongly Reduced Naive T Cells Support Intact Memory T Cell Compartment in Ataxia Telangiectasia.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.686333
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- Publication type:
- Article
Modeling Influencing Factors in B-Cell Reconstitution After Hematopoietic Stem Cell Transplantation in Children.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. N.PAG, doi. 10.3389/fimmu.2021.684147
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- Publication type:
- Article
Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.603972
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- Publication type:
- Article
Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.
- Published in:
- Clinical & Experimental Immunology, 2024, v. 215, n. 2, p. 160, doi. 10.1093/cei/uxad110
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- Publication type:
- Article
Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 3, p. 618, doi. 10.1007/s10875-021-01201-5
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- Publication type:
- Article