Found: 17
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Security versus Openness: The Case of Universities.
- Published in:
- Issues in Science & Technology, 2003, v. 19, n. 4, p. 89
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- Publication type:
- Article
Molecular Analysis of Goodpasture's Disease Following Hematopoietic Stem Cell Transplant in a Pediatric Patient, Recalls the Conformeropathy of Wild-Type Anti-GBM Disease.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02659
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- Publication type:
- Article
COVID‐19 in children. II: Pathogenesis, disease spectrum and management.
- Published in:
- Journal of Paediatrics & Child Health, 2022, v. 58, n. 1, p. 46, doi. 10.1111/jpc.15811
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- Publication type:
- Article
COVID‐19 in children: I. Epidemiology, prevention and indirect impacts.
- Published in:
- Journal of Paediatrics & Child Health, 2022, v. 58, n. 1, p. 39, doi. 10.1111/jpc.15791
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- Publication type:
- Article
Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiency.
- Published in:
- 2021
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- Publication type:
- journal article
Salicylate elimination diets in children: is food restriction supported by the evidence?
- Published in:
- Medical Journal of Australia, 2013, v. 198, n. 11, p. 600, doi. 10.5694/mja12.11255
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- Publication type:
- Article
Pyrin variant E148Q potentiates inflammasome activation and the effect of pathogenic mutations in cis.
- Published in:
- Rheumatology, 2024, v. 63, n. 3, p. 882, doi. 10.1093/rheumatology/kead376
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- Publication type:
- Article
Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Filaggrin-Associated Atopic Skin, Eye, Airways, and Gut Disease, Modifying the Presentation of X-Linked Reticular Pigmentary Disorder (XLPDR)
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 1, p. 1, doi. 10.1007/s10875-023-01637-x
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- Publication type:
- Article
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 1, p. 119, doi. 10.1007/s10875-021-01152-x
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- Publication type:
- Article
Intrinsic Defects in B Cell Development and Differentiation, T Cell Exhaustion and Altered Unconventional T Cell Generation Characterize Human Adenosine Deaminase Type 2 Deficiency.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 8, p. 1915, doi. 10.1007/s10875-021-01141-0
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- Publication type:
- Article
The Clinical Immunogenomics Research Consortium Australasia (CIRCA): a Distributed Network Model for Genomic Healthcare Delivery.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Diversity of XMEN Disease: Description of 2 Novel Variants and Analysis of the Lymphocyte Phenotype.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 2, p. 299, doi. 10.1007/s10875-019-00732-2
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- Publication type:
- Article
Salicylate elimination diets in children: is food restriction supported by the evidence?
- Published in:
- 2013
- By:
- Publication type:
- Letter
IN REPLY.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Severe COVID‐19 represents an undiagnosed primary immunodeficiency in a high proportion of infected individuals.
- Published in:
- Clinical & Translational Immunology, 2022, v. 11, n. 4, p. 1, doi. 10.1002/cti2.1365
- By:
- Publication type:
- Article
A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 8, p. 1, doi. 10.1007/s10875-024-01774-x
- By:
- Publication type:
- Article