Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference16 articles.
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2. Combined immunodeficiency associated with DOCK8 mutations;Zhang;N. Engl. J. Med.,2009
3. DOCK8 deficiency;Su;Ann. N. Y. Acad. Sci.,2011
4. Clinical manifestations of hyper IgE syndromes;Freeman;Dis. Markers,2010
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1. A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries;Journal of Clinical Immunology;2024-08-05
2. Phenotypic and Genotypic Spectrum of Children with Autosomal Recessive Hyperimmunoglobulin E Syndrome Caused by DOCK8 Mutation: A Systematic Review of Case Reports;Indian Pediatrics Case Reports;2024-07
3. A systematic review regarding the prevalence of malignancy in patients with the hyper-IgE syndrome;Clinical and Experimental Medicine;2023-11-04
4. Emerging spectrum of DOCK8 deficiency in children and challenges associated with providing treatment: experience from a tertiary referral centre in India;2023-09-26
5. Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report;Cureus;2023-08-12
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