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Last Updated : 06/20/2022

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Found 11 publications

Primary atopic disorders and chronic skin disease.

Investigating the Variation of TREC/KREC in Combined Immunodeficiencies.

Dupilumab for STAT3-Hyper-IgE Syndrome With Refractory Intestinal Complication.

Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report.

Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.

Peripheral immune profile of children with Talaromyces marneffei infections: a retrospective analysis of 21 cases.

Pulmonary Infections and Surgical Complications in a Young Girl with Signal Transducer and Activator of Transcription 3 Loss-of-Function Mutation Hyperimmunoglobulin E Syndrome: A Case Report.

Clinical Profile of Hyper-IgE Syndrome in India.

Differential responses to folic acid in an established keloid fibroblast cell line are mediated by JAK1/2 and STAT3.

Hyper-Immunoglobulin E Syndrome and Squamous Cell Carcinoma of the Lower Lip: A Case Report.

Autosomal recessive hyper-IgE syndrome successfully treated with hematopoietic stem cell transplantation.

Showing 1-11 of 11

Last Updated : 06/20/2022