Found: 10
Select item for more details and to access through your institution.
Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.972746
- By:
- Publication type:
- Article
Trends in TREC values according to age and gender in Chinese children and their clinical applications.
- Published in:
- European Journal of Pediatrics, 2022, v. 181, n. 2, p. 529, doi. 10.1007/s00431-021-04223-8
- By:
- Publication type:
- Article
Clinical characteristics of early-onset paediatric systemic lupus erythematosus in a single centre in China.
- Published in:
- Rheumatology, 2023, v. 62, n. 10, p. 3373, doi. 10.1093/rheumatology/kead086
- By:
- Publication type:
- Article
Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome.
- Published in:
- Immunologic Research, 2016, v. 64, n. 2, p. 497, doi. 10.1007/s12026-015-8723-4
- By:
- Publication type:
- Article
Novel DOCK8 gene mutations lead to absence of protein expression in patients with hyper-IgE syndrome.
- Published in:
- Immunologic Research, 2016, v. 64, n. 1, p. 260, doi. 10.1007/s12026-015-8745-y
- By:
- Publication type:
- Article
An early-onset SLE patient with a novel paternal inherited BACH2 mutation.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 6, p. 1367, doi. 10.1007/s10875-023-01506-7
- By:
- Publication type:
- Article
A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 5, p. 933, doi. 10.1007/s10875-023-01453-3
- By:
- Publication type:
- Article
IL-21 Rescues the Defect of IL-10-Producing Regulatory B Cells and Improves Allergic Asthma in DOCK8 Deficient Mice.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.695596
- By:
- Publication type:
- Article
Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by G6PC3 Mutations.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.699743
- By:
- Publication type:
- Article
A Novel Homozygous Mutation Destabilizes IKKβ and Leads to Human Combined Immunodeficiency.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.517544
- By:
- Publication type:
- Article