Found: 33
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Thymosin Alpha 1 Mitigates Cytokine Storm in Blood Cells From Coronavirus Disease 2019 Patients.
- Published in:
- Open Forum Infectious Diseases, 2021, v. 8, n. 1, p. 1, doi. 10.1093/ofid/ofaa588
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- Publication type:
- Article
Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 22, p. 8604, doi. 10.3390/ijms21228604
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- Publication type:
- Article
Positive impacts in social life cycle assessment: state of the art and the way forward.
- Published in:
- International Journal of Life Cycle Assessment, 2018, v. 23, n. 3, p. 406, doi. 10.1007/s11367-016-1169-7
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- Publication type:
- Article
Systematic literature review in social life cycle assessment.
- Published in:
- International Journal of Life Cycle Assessment, 2018, v. 23, n. 3, p. 422, doi. 10.1007/s11367-016-1135-4
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- Publication type:
- Article
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.952715
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- Publication type:
- Article
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.919237
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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
- By:
- Publication type:
- journal article
Needs of caregivers’ patients with dementia
- Published in:
- 2009
- By:
- Publication type:
- Abstract
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome.
- Published in:
- Scientific Reports, 2017, v. 7, n. 1, p. 1, doi. 10.1038/s41598-017-12069-0
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- Publication type:
- 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
Microgravity Promotes Differentiation and Meiotic Entry of Postnatal Mouse Male Germ Cells.
- Published in:
- PLoS ONE, 2010, v. 5, n. 2, p. 1, doi. 10.1371/journal.pone.0009064
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- Publication type:
- Article
Lymphoid EVA1 Expression Is Required for DN1-DN3 Thymocytes Transition.
- Published in:
- PLoS ONE, 2009, v. 4, n. 10, p. 1, doi. 10.1371/journal.pone.0007586
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- Publication type:
- Article
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
Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00316
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- Publication type:
- Article
Thymic Epithelium Abnormalities in DiGeorge and Down Syndrome Patients Contribute to Dysregulation in T Cell Development.
- Published in:
- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00447
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- Publication type:
- Article
Use of dupilumab for atopic dermatitis in pediatric and young adult patients with inborn errors of immunity.
- Published in:
- Pediatric Allergy & Immunology, 2024, v. 35, n. 8, p. 1, doi. 10.1111/pai.14215
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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
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
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection.
- Published in:
- 2017
- 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
Author Correction: Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Author Correction: Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
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
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
Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients.
- Published in:
- Pediatric Allergy & Immunology, 2015, v. 26, n. 6, p. 591, doi. 10.1111/pai.12420
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- Publication type:
- Article
Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections.
- Published in:
- Pediatric Allergy & Immunology, 2002, v. 13, n. 6, p. 443, doi. 10.1034/j.1399-3038.2002.02088.x
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- Publication type:
- Article