Works matching DE "AGAMMAGLOBULINEMIA"
Results: 1182
Bruton tyrosine kinase gene mutations in Argentina (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #602 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/602.pdf).
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- Human Mutation, 2003, v. 21, n. 4, p. 451, doi. 10.1002/humu.9131
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- Article
Bruton tyrosine kinase gene mutations in ArgentinaCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #602 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/602.pdf.
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- Human Mutation, 2003, v. 21, n. 4, p. 451, doi. 10.1002/humu.9131
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- Article
Evolution of immunoglobulin and mannose binding protein levels after renal transplantation: association with infectious complications.
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- Transplant International, 2008, v. 21, n. 1, p. 57, doi. 10.1111/j.1432-2277.2007.00556.x
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- Article
Mesenchymal Stem/Stromal Cells Overexpressing CXCR4 R334X Revealed Enhanced Migration: A Lesson Learned from the Pathogenesis of WHIM Syndrome.
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- Cell Transplantation, 2021, v. 30, p. 1, doi. 10.1177/09636897211054498
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- Article
Reply to 'On the implications of polyclonal B cell activation'.
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- Nature Immunology, 2003, v. 4, n. 10, p. 932, doi. 10.1038/ni1003-932
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Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency.
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- Nature Immunology, 2003, v. 4, n. 3, p. 261, doi. 10.1038/ni902
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Lack of IgA in Cu-deficient patients.
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- Nature Immunology, 2002, v. 3, n. 7, p. 595, doi. 10.1038/ni0702-595
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Direct inhibition of Bruton's tyrosine kinase by IBtk, a Btk-binding protein.
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- Nature Immunology, 2001, v. 2, n. 10, p. 939, doi. 10.1038/ni1001-939
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- Article
Profound Hypogammaglobulinemia 7 Years after Treatment for Indolent Lymphoma.
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- Cancer Investigation, 2008, v. 26, n. 4, p. 431, doi. 10.1080/07357900701809068
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- Article
B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting.
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- Science Immunology, 2024, v. 9, n. 98, p. 1, doi. 10.1126/sciimmunol.add4874
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- Article
Human T-bet governs the generation of a distinct subset of CD11c<sup>high</sup>CD21<sup>low</sup> B cells.
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- Science Immunology, 2022, v. 7, n. 73, p. 1, doi. 10.1126/sciimmunol.abq3277
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- Article
桂枝芍药知母汤联合甲氨蝶呤对类风湿性关节炎患者中医证候评分、 血清炎性因子及免疫球蛋白的影响.
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- Progress in Modern Biomedicine, 2020, v. 12, n. 24, p. 4641, doi. 10.13241/j.cnki.pmb.2020.24.009
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- Article
Chronic graft vs. host disease and hypogammaglobulinemia predict a lower immunological response to the BNT162b2 mRNA COVID-19 vaccine after allogeneic hematopoietic stem cell transplantation.
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- European Review for Medical & Pharmacological Sciences, 2022, v. 26, n. 23, p. 8984
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- Article
Associations between Antiepileptic Use and Hypogammaglobulinaemia: Findings from a Population-Based Case-Control Study Using Data Linkage.
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- Neuroepidemiology, 2023, v. 57, n. 6, p. 355, doi. 10.1159/000533699
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REGIONAL VETERINARY LABORATORIES REPORT.
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- Veterinary Ireland Journal, 2018, v. 8, n. 5, p. 290
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- Article
Pneumocystis pneumonia with hypogammaglobulinemia in a pediatric patient who underwent heart transplantation.
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- Transplant Infectious Disease, 2021, v. 23, n. 4, p. 1, doi. 10.1111/tid.13571
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- Article
Impact of immunoglobulin G2 subclass level on late‐onset bacterial infection after allogeneic hematopoietic stem cell transplantation.
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- Transplant Infectious Disease, 2019, v. 21, n. 3, p. N.PAG, doi. 10.1111/tid.13086
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A national survey of screening and management of hypogammaglobulinemia in Canadian transplantation centers.
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- Transplant Infectious Disease, 2017, v. 19, n. 4, p. n/a, doi. 10.1111/tid.12706
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- Article
B cell M-CLL clones retain selection against replacement mutations in their immunoglobulin gene framework regions.
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- Frontiers in Oncology, 2023, v. 13, p. 1, doi. 10.3389/fonc.2023.1115361
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Treatment for a B-cell acute lymphoblastic leukemia patient carrying a rare TP53 c.C275T mutation: A case report.
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- Frontiers in Oncology, 2023, v. 13, p. 1, doi. 10.3389/fonc.2022.1018250
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Immune response of heterologous versus homologous prime-boost regimens with adenoviral vectored and mRNA COVID-19 vaccines in immunocompromised patients.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1187880
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Case Report: A novel IRF2BP2 mutation in an IEI patient with recurrent infections and autoimmune disorders.
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- Frontiers in Immunology, 2023, p. 01, doi. 10.3389/fimmu.2023.967345
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T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency – a 22- month follow-up.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1146500
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Should treatment of hypogammaglobulinemia with immunoglobulin replacement therapy (IgRT) become standard of care in patients with chronic lymphocytic leukemia?
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- Frontiers in Immunology, 2023, p. 01, doi. 10.3389/fimmu.2023.1062376
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SARS-CoV-2 spike antibody concentration in gamma globulin products from high-prevalence COVID-19 countries are transmitted to X-linked agammaglobulinemia patients.
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- Frontiers in Immunology, 2023, v. 14, p. 01, doi. 10.3389/fimmu.2023.1156823
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Cellular and humoral immunogenicity of the COVID- 19 vaccine and COVID-19 disease severity in individuals with immunodeficiency.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1131604
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Characterization of the tumor-infiltrating immune repertoire in muscle invasive bladder cancer.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.986598
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Analysis of IGH allele content in a sample group of rheumatoid arthritis patients demonstrates unrevealed population heterogeneity.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1073414
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Standard immunosuppressive treatment reduces regulatory B cells in children with autoimmune liver disease.
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- Frontiers in Immunology, 2023, v. 13, p. 1
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Case report: Evolution of pulmonary manifestations and virological markers in critical COVID-19 infection in Bruton's agammaglobulinemia.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1057065
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Comparison of pulmonary lesions using lung ultrasound and high-resolution computed tomography in adult patients with primary humoral immunodeficiencies.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1031258
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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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Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency.
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- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.910021
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A novel CARD11 germline mutation in a Chinese patient of B cell expansion with NF-κB and T cell anergy (BENTA) and literature review.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.943027
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Newborn screening for severe combined immunodeficiency: The results of the first pilot TREC and KREC study in Ukraine with involving of 10,350 neonates.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.999664
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Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.952715
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Altered Circulating Immune Cell Distribution in Traumatic Spinal Cord Injury Patients in Relation to Clinical Parameters.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.873315
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Cellular Mechanisms Underlying B Cell Abnormalities in Patients With Gain-of-Function Mutations in the PIK3CD Gene.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.890073
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Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report.
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- 2022
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- Case Study
B- and T-Cell Subset Abnormalities in Monogenic Common Variable Immunodeficiency.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.912826
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New diagnostic criteria for common variable immune deficiency ( CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin.
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- Clinical & Experimental Immunology, 2013, v. 174, n. 2, p. 203, doi. 10.1111/cei.12178
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CD27<sup>+</sup> B cells from a subgroup of common variable immunodeficiency patients are less sensitive to apoptosis rescue regardless of interleukin-21 signalling.
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- Clinical & Experimental Immunology, 2013, v. 174, n. 1, p. 97, doi. 10.1111/cei.12150
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Importance of B cell co-stimulation in CD4.
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- Clinical & Experimental Immunology, 2011, v. 164, n. 3, p. 381, doi. 10.1111/j.1365-2249.2011.04377.x
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Do ribosomopathies explain some cases of common variable immunodeficiency?
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- Clinical & Experimental Immunology, 2011, v. 163, n. 1, p. 96, doi. 10.1111/j.1365-2249.2010.04280.x
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Serum bactericidal activity against Helicobacter pylori in patients with hypogammaglobulinaemia.
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- Clinical & Experimental Immunology, 2009, v. 156, n. 3, p. 434, doi. 10.1111/j.1365-2249.2009.03909.x
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Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency.
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- Clinical & Experimental Immunology, 2008, v. 153, n. 3, p. 324, doi. 10.1111/j.1365-2249.2008.03700.x
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Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model.
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- Clinical & Experimental Immunology, 2008, v. 152, n. 1, p. 33, doi. 10.1111/j.1365-2249.2008.03589.x
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A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical disease.
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- Clinical & Experimental Immunology, 2008, v. 152, n. 1, p. 39, doi. 10.1111/j.1365-2249.2008.03593.x
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Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients.
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- Clinical & Experimental Immunology, 2006, v. 143, n. 2, p. 373, doi. 10.1111/j.1365-2249.2006.02999.x
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Gene expression analysis of peripheral T cells in a subgroup of common variable immunodeficiency shows predominance of CCR7<sup>–</sup> effector-memory T cells.
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- Clinical & Experimental Immunology, 2004, v. 138, n. 2, p. 278, doi. 10.1111/j.1365-2249.2004.02630.x
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- Article