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Hodgkin Lymphoma after Disseminated Mycobacterium genavense Infection, Germany.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Pneumocystis jirovecii pneumonia in a baby with hyper-IgE syndrome.
- Published in:
- European Journal of Pediatrics, 2010, v. 169, n. 1, p. 35, doi. 10.1007/s00431-009-0973-5
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- Publication type:
- Article
CD161 expression characterizes a subpopulation of human regulatory T cells that produces IL-17 in a STAT3-dependent manner.
- Published in:
- European Journal of Immunology, 2013, v. 43, n. 8, p. 2043, doi. 10.1002/eji.201243296
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- Publication type:
- Article
The Genetics of Hypogammaglobulinemia.
- Published in:
- Current Allergy & Asthma Reports, 2004, v. 4, n. 5, p. 349, doi. 10.1007/s11882-004-0083-4
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- Publication type:
- Article
CVID-associated TACI mutations affect autoreactive B cell selection and activation.
- Published in:
- Journal of Clinical Investigation, 2013, v. 123, n. 10, p. 4283, doi. 10.1172/JCI69854
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- Publication type:
- Article
Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1011646
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- Publication type:
- Article
Multi-omics analysis of naïve B cells of patients harboring the C104R mutation in TACI.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.938240
- By:
- Publication type:
- Article
A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14.
- Published in:
- Nature Medicine, 2007, v. 13, n. 1, p. 38, doi. 10.1038/nm1528
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- Publication type:
- Article
FAS mutations are an uncommon cause of immune thrombocytopenia in children and adults without additional features of immunodeficiency.
- Published in:
- British Journal of Haematology, 2019, v. 186, n. 6, p. e163, doi. 10.1111/bjh.15979
- By:
- Publication type:
- Article
Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.
- Published in:
- 2007
- By:
- Publication type:
- Letter
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940
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- Publication type:
- Article
Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA Mutation.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Autoantibodies against BAFF, APRIL or IL21 - an alternative pathogenesis for antibody-deficiencies?
- Published in:
- BMC Immunology, 2017, v. 18, p. 1, doi. 10.1186/s12865-017-0217-9
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- Publication type:
- Article
Evidence for non-neutralizing autoantibodies against IL-10 signalling components in patients with inflammatory bowel disease.
- Published in:
- BMC Immunology, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2172-15-10
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- Publication type:
- Article
Screening of functional and positional candidate genes in families with common variable immunodeficiency.
- Published in:
- BMC Immunology, 2008, v. 9, p. 1, doi. 10.1186/1471-2172-9-3
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- Publication type:
- Article
IL-10 and IL-10 receptor defects in humans.
- Published in:
- Annals of the New York Academy of Sciences, 2011, v. 1246, n. 1, p. 102, doi. 10.1111/j.1749-6632.2011.06339.x
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- Publication type:
- Article
Is It Safe to Switch From Intravenous Immunoglobulin to Subcutaneous Immunoglobulin in Patients With Common Variable Immunodeficiency and Autoimmune Thrombocytopenia?
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.01656
- By:
- Publication type:
- Article
"Immune TOR-opathies," a Novel Disease entity in Clinical Immunology.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00966
- By:
- Publication type:
- Article
Rapid Flow Cytometry-Based test for the diagnosis of Lipopolysaccharide Responsive Beige-Like Anchor (LRBA) deficiency.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00720
- By:
- Publication type:
- Article
The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Diagnostic Yield and Therapeutic Consequences of Targeted Next-Generation Sequencing in Sporadic Primary Immunodeficiency.
- Published in:
- International Archives of Allergy & Immunology, 2022, v. 183, n. 3, p. 337, doi. 10.1159/000519199
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- Publication type:
- Article
Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.
- Published in:
- Human Genetics, 2006, v. 118, n. 6, p. 725, doi. 10.1007/s00439-005-0101-1
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- Publication type:
- Article
Altered Microbiota, Impaired Quality of Life, Malabsorption, Infection, and Inflammation in CVID Patients With Diarrhoea.
- Published in:
- Frontiers in Immunology, 2020, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.01654
- By:
- Publication type:
- Article
Late-Onset Antibody Deficiency Due to Monoallelic Alterations in NFKB1.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02618
- By:
- Publication type:
- Article
Corrigendum: Assessing the Functional Relevance of Variants in the IKAROS Family Zinc Finger Protein 1 (IKZF1) in a Cohort of Patients With Primary Immunodeficiency.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice (Small 38/2024).
- Published in:
- Small, 2024, v. 20, n. 38, p. 1, doi. 10.1002/smll.202470280
- By:
- Publication type:
- Article
Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice.
- Published in:
- Small, 2024, v. 20, n. 38, p. 1, doi. 10.1002/smll.202311834
- By:
- Publication type:
- Article
STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 3, p. 352, doi. 10.1038/ejhg.2008.169
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- Publication type:
- Article
Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 7, p. 867, doi. 10.1038/sj.ejhg.5201634
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- Publication type:
- Article
Evaluation and Management of Deficiency of Adenosine Deaminase 2: An International Consensus Statement.
- Published in:
- JAMA Network Open, 2023, v. 6, n. 5, p. e2315894, doi. 10.1001/jamanetworkopen.2023.15894
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- Publication type:
- Article
What did we learn from CTLA‐4 insufficiency on the human immune system?
- Published in:
- Immunological Reviews, 2019, v. 287, n. 1, p. 33, doi. 10.1111/imr.12721
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- Publication type:
- Article
The role of costimulation in antibody deficiencies: ICOS and common variable immunodeficiency.
- Published in:
- Immunological Reviews, 2009, v. 229, n. 1, p. 101, doi. 10.1111/j.1600-065X.2009.00764.x
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- Publication type:
- Article
Hyper-IgE syndromes.
- Published in:
- Immunological Reviews, 2005, v. 203, n. 1, p. 244, doi. 10.1111/j.0105-2896.2005.00228.x
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- Publication type:
- Article
Future Directions in the Diagnosis and Treatment of APDS and IEI: a Survey of German IEI Centers.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1279652
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- Publication type:
- Article
An update on the hyper-IgE syndromes.
- Published in:
- Arthritis Research & Therapy, 2012, v. 14, n. 6, p. 228, doi. 10.1186/ar4069
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- Publication type:
- Article
B-cells absence in patients diagnosed as inborn errors of immunity: a registry-based study.
- Published in:
- Immunogenetics, 2024, v. 76, n. 3, p. 189, doi. 10.1007/s00251-024-01342-y
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- Publication type:
- Article
The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88.
- Published in:
- Nature Immunology, 2010, v. 11, n. 9, p. 836, doi. 10.1038/ni.1914
- By:
- Publication type:
- Article
Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency.
- Published in:
- Nature Immunology, 2003, v. 4, n. 3, p. 261, doi. 10.1038/ni902
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- Publication type:
- Article
DOCK8 deficiency in six Iranian patients.
- Published in:
- Clinical Case Reports, 2016, v. 4, n. 6, p. 593, doi. 10.1002/ccr3.574
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- Publication type:
- Article
Interdisciplinary approach towards a systems medicine toolbox using the example of inflammatory diseases.
- Published in:
- Briefings in Bioinformatics, 2017, v. 18, n. 3, p. 479, doi. 10.1093/bib/bbw024
- By:
- Publication type:
- Article
Inborn errors of immunity associated with defects of self‐tolerance checkpoints: The CD28 family.
- Published in:
- Pediatric Allergy & Immunology, 2022, v. 33, n. 12, p. 1, doi. 10.1111/pai.13886
- By:
- Publication type:
- Article
A Pathogenic Missense Variant in NFKB1 Causes Common Variable Immunodeficiency Due to Detrimental Protein Damage.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.621503
- By:
- Publication type:
- Article
Important Factors Influencing Severity of Common Variable Immunodeficiency.
- Published in:
- Archives of Iranian Medicine (AIM), 2016, v. 19, n. 8, p. 544
- By:
- Publication type:
- Article
Correction to: Functional Relevance of CTLA4 Variants: an Upgraded Approach to Assess CTLA4‑Dependent Transendocytosis by Flow Cytometry.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Functional Relevance of CTLA4 Variants: an Upgraded Approach to Assess CTLA4-Dependent Transendocytosis by Flow Cytometry.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 8, p. 2076, doi. 10.1007/s10875-023-01582-9
- By:
- Publication type:
- Article
Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 7, p. 1611, doi. 10.1007/s10875-023-01530-7
- By:
- Publication type:
- Article
JAKs and STATs from a Clinical Perspective: Loss-of-Function Mutations, Gain-of-Function Mutations, and Their Multidimensional Consequences.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 6, p. 1326, doi. 10.1007/s10875-023-01483-x
- By:
- Publication type:
- Article
Fecal Immunoglobulin Levels as a Modifier of the Gut Microbiome in Patients with Common Variable Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 6, p. 1208, doi. 10.1007/s10875-023-01469-9
- By:
- Publication type:
- Article
A Toolkit for Monitoring Immunoglobulin G Levels from Dried Blood Spots of Patients with Primary Immunodeficiencies.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 6, p. 1185, doi. 10.1007/s10875-023-01464-0
- By:
- Publication type:
- Article
Sequencing the B Cell Receptor Repertoires of Antibody-Deficient Individuals With and Without Infection Susceptibility.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 5, p. 940, doi. 10.1007/s10875-023-01448-0
- By:
- Publication type:
- Article