Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry-Reference-Cited by-同舟云学术

Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry

Published:2018-05 Issue:3 Volume:6 Page:996-1001
ISSN:2213-2198
Container-title:The Journal of Allergy and Clinical Immunology: In Practice
language:en
Short-container-title:The Journal of Allergy and Clinical Immunology: In Practice

Author:

Gernez Yael^ORCID,Freeman Alexandra F.,Holland Steven M.,Garabedian Elizabeth,Patel Niraj C.,Puck Jennifer M.,Sullivan Kathleen E.,Akhter Javeed,Secord Elizabeth,Chen Karin,Buckley Rebecca,Haddad Elie,Ochs Hans D.,Fuleihan Ramsay,Routes John^ORCID,Muskat Mica,Lugar Patricia,Mancini Julien^ORCID,Cunningham-Rundles Charlotte

Funder

National Institutes of Health (NIH)

Publisher

Elsevier BV

Subject

Immunology and Allergy

Reference40 articles.

1. Job's syndrome. Recurrent, “cold”, staphylococcal abscesses;Davis;Lancet,1966

2. Extreme hyperimmunoglobulinemia E and undue susceptibility to infection;Buckley;Pediatrics,1972

3. Hyper-IgE syndrome with recurrent infections—an autosomal dominant multisystem disorder;Grimbacher;N Engl J Med,1999

4. Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity;Puel;Science,2011

5. Bone density and fractures in autosomal dominant hyper IgE syndrome;Sowerwine;J Clin Immunol,2014

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