Found: 29
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Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency.
- Published in:
- European Journal of Immunology, 2022, v. 52, n. 7, p. 1171, doi. 10.1002/eji.202149480
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- Publication type:
- Article
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 3, p. 818, doi. 10.3390/jcm9030818
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- Publication type:
- Article
Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.799564
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- Publication type:
- Article
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children.
- Published in:
- 2019
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- Publication type:
- journal article
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00130
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- Publication type:
- Article
Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ<sup>+</sup> T and B Cells.
- Published in:
- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01893
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- Publication type:
- Article
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin Content.
- Published in:
- 2017
- By:
- Publication type:
- Correction Notice
IPINeT Ped-unPAD Study: Goals, Design, and Preliminary Results.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 15, p. 4321, doi. 10.3390/jcm13154321
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- Publication type:
- Article
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 13, p. 4206, doi. 10.3390/jcm12134206
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- Publication type:
- Article
Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02471
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- Publication type:
- Article
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network.
- Published in:
- Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.01908
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- Publication type:
- Article
Dual-regulated Lentiviral Vector for Gene Therapy of X-linked Chronic Granulomatosis.
- Published in:
- Molecular Therapy, 2014, v. 22, n. 8, p. 1472, doi. 10.1038/mt.2014.87
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- Publication type:
- Article
Humoral and Cellular Response Following Vaccination With the BNT162b2 mRNA COVID-19 Vaccine in Patients Affected by Primary Immunodeficiencies.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.727850
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- Publication type:
- Article
Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.708837
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- Publication type:
- Article
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 2, p. 299, doi. 10.1007/s10875-021-01159-4
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- Publication type:
- Article
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 1, p. 130, doi. 10.1007/s10875-021-01130-3
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- Publication type:
- Article
Urogenital Abnormalities in Adenosine Deaminase Deficiency.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 4, p. 610, doi. 10.1007/s10875-020-00777-8
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- Publication type:
- Article
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection.
- Published in:
- 2017
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- Publication type:
- Letter
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 4, p. 373, doi. 10.1007/s10875-015-0154-4
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- Publication type:
- Article
Pancytopenia and severe sepsis in an adult case of congenital X-linked agammaglobulinemia (XLA).
- Published in:
- 2010
- By:
- Publication type:
- Letter
Immunological Aspects of X-Linked Chronic Granulomatous Disease Female Carriers.
- Published in:
- Antioxidants, 2021, v. 10, n. 6, p. 891, doi. 10.3390/antiox10060891
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- Publication type:
- Article
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long‐known gene.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 5, p. 713, doi. 10.1002/mgg3.391
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- Publication type:
- Article
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin Content
- Published in:
- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.00798
- By:
- Publication type:
- Article
Partial T cell defects and expanded CD56<sup>bright</sup> NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene.
- Published in:
- Journal of Leukocyte Biology, 2020, v. 108, n. 2, p. 739, doi. 10.1002/JLB.5MA0220-239R
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- Publication type:
- Article
A variable degree of autoimmunity in the pedigree of a patient with type 1 diabetes homozygous for the PTPN22 1858 T variant.
- Published in:
- Pediatric Diabetes, 2013, v. 14, n. 4, p. 304, doi. 10.1111/j.1399-5448.2012.00891.x
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- Publication type:
- Article
Inflammatory bowel disease in chronic granulomatous disease: An emerging problem over a twenty years' experience.
- Published in:
- Pediatric Allergy & Immunology, 2017, v. 28, n. 8, p. 801, doi. 10.1111/pai.12814
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- Publication type:
- Article
Late-onset combined immune deficiency due to LIGIV mutations in a 12-year-old patient.
- Published in:
- Pediatric Allergy & Immunology, 2017, v. 28, n. 2, p. 203, doi. 10.1111/pai.12684
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- Publication type:
- Article
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects.
- Published in:
- Pediatric Allergy & Immunology, 2016, v. 27, n. 3, p. 242, doi. 10.1111/pai.12527
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- Publication type:
- Article
Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1276697
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- Publication type:
- Article