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The Journal of Allergy and Clinical Immunology|December 17, 2009
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndromeKarin R Engelhardt, Sean McGhee, Sabine Winkler, et al.Clinical and Experimental Immunology|May 31, 2022
Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UKAdrian M Shields, Ariharan Anantharachagan, Gururaj Arumugakani, et al.The Journal of Allergy and Clinical Immunology|April 1, 2014
BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policiesBeatriz E Marciano, Chiung-Yu Huang, Gyan Joshi, et al.Journal of Clinical Immunology|January 29, 2015
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patientsSusanne E Aydin, Sara Sebnem Kilic, Caner Aytekin, et al.The Journal of Allergy and Clinical Immunology|October 5, 2016
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantationM Teresa de la Morena, David Leonard, Troy R Torgerson, et al.Pageof 5