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The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency

<p>Abstract</p> <p>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...

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Detalhes bibliográficos
Main Authors: Szczawinska-Poplonyk Aleksandra, Kycler Zdzislawa, Pietrucha Barbara, Heropolitanska-Pliszka Edyta, Breborowicz Anna, Gerreth Karolina
Formato: Artigo
Idioma:Inglês
Publicado em: BMC 2011-11-01
Colecção:Orphanet Journal of Rare Diseases
Acesso em linha:http://www.ojrd.com/content/6/1/76
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