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The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency
The hyper-IgE syndromes are rare, complex primary immunodeficiencies characterized by clinical manifestation diversity, by particular susceptibility to staphylococcal and mycotic infections as well as by a heterogeneous genetic origin. Two distinct entities - the classical hyper-IgE syndrome which i...
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| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3226432/ https://ncbi.nlm.nih.gov/pubmed/22085750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-76 |
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