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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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主要な著者: | , , , , , |
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フォーマット: | Artigo |
言語: | Inglês |
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BMC
2011-11-01
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シリーズ: | Orphanet Journal of Rare Diseases |
オンライン・アクセス: | http://www.ojrd.com/content/6/1/76 |
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