A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis

Author:

Kasap Nurhan,Celik Velat,Isik Sakine,Cennetoglu Pakize,Kiykim Ayca,Eltan Sevgi Bilgic,Nain Ercan,Ogulur Ismail,Baser Dilek,Akkelle Emre,Celiksoy Mehmet Halil,Kocamis Burcu,Cipe Funda Erol,Yucelten Ayse Deniz,Karakoc-Aydiner Elif,Ozen Ahmet,Baris Safa

Funder

Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference41 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. Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome;Woellner;J. Allergy Clin. Immunol.,2010

5. Genetic linkage of hyper-IgE syndrome to chromosome 4;Grimbacher;Am. J. Hum. Genet.,1999

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