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Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-34953-z
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- Publication type:
- Article
Impaired memory B‐cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper‐IgE syndrome.
- Published in:
- Allergy, 2019, v. 74, n. 12, p. 2394, doi. 10.1111/all.13969
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- Publication type:
- Article
Lung disease in STAT3 hyper‐IgE syndrome requires intense therapy.
- Published in:
- Allergy, 2019, v. 74, n. 9, p. 1691, doi. 10.1111/all.13753
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- Publication type:
- Article
Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children.
- Published in:
- Pediatric Allergy & Immunology, 2016, v. 27, n. 2, p. 177, doi. 10.1111/pai.12512
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- Publication type:
- Article
Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential.
- Published in:
- 2020
- By:
- Publication type:
- journal article