The Hyper-IgE Syndrome. Two cases and review of the literature
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-4362.2001.01271.x/fullpdf
Reference39 articles.
1. Previously undiagnosed hyper-IgE syndrome in an adult with multiple systemic fungal infections☆☆☆★
2. Variant of Hyper-IgE Syndrome: The Differentiation from Atopic Dermatitis Is Important because of Treatment and Prognosis
3. DEFECT IN NEUTROPHIL GRANULOCYTE CHEMOTAXIS IN JOB'S SYNDROME OF RECURRENT "COLD" STAPHYLOCOCCAL ABSCESSES
4. 4 RA Thompson, and DS. Kumararante, Hyper-IgE syndrome and H2-receptor blockade.Lancet. ;, 1989 .
5. 5 H Donabedian, and J Gallin . The hyperimmunoglobulin E recurrent infection (Job's) syndrome. A Review of the NIH Experience and the Literature . Medicine (Baltimore)1983 ; 62 : 195 -208.
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1. Hyperimmunoglobulin E syndrome: Genetics, immunopathogenesis, clinical findings, and treatment modalities;Journal of Research in Medical Sciences;2017
2. Sindrome de Hiper-Inmunoglobulina E;Piel;2014-11
3. Hyper-IgE Syndrome;Atlas of Genetic Diagnosis and Counseling;2012
4. The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency;Orphanet Journal of Rare Diseases;2011
5. 40 Cutaneous infiltrates – non-lymphoid;Weedon's Skin Pathology;2010
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