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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Detaylı Bibliyografya
Asıl Yazarlar: Szczawinska-Poplonyk, Aleksandra, Kycler, Zdzislawa, Pietrucha, Barbara, Heropolitanska-Pliszka, Edyta, Breborowicz, Anna, Gerreth, Karolina
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2011
Konular:
Review
Online Erişim: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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