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Clinical Immunology (Orlando, Fla.)|December 19, 2025
Clinical spectrum of Wiskott-Aldrich syndrome carriers: Self-reported survey of 193 carriersShanmuganathan Chandrakasan, Adrianna Westbrook, Linda M Griffith, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2014
Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts, William T Shearer, Thomas A Fleisher, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2013
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiencyYu Nee Lee, Francesco Frugoni, Kerry Dobbs, et al.
The Journal of Allergy and Clinical Immunology. in Practice|June 4, 2026
IMPACT (Immune Monitoring and Phenotype Assessment of Clinical Trajectory) for Patients with Inborn Errors of Immunity from the Primary Immune Deficiency Treatment Consortium (PIDTC)Danielle E Arnold, Hesham Eissa, Elizabeth Dunn, et al.
Nature Genetics|June 1, 2005
Gains of glycosylation comprise an unexpectedly large group of pathogenic mutationsGuillaume Vogt, Ariane Chapgier, Kun Yang, et al.
The Journal of Experimental Medicine|June 16, 2010
Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiencyJolan E Walter, Francesca Rucci, Laura Patrizi, et al.
The New England Journal of Medicine|April 18, 2019
Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1Ewelina Mamcarz, Sheng Zhou, Timothy Lockey, et al.
The Journal of Allergy and Clinical Immunology|August 20, 2022
Aberrant T-cell exhaustion in severe combined immunodeficiency survivors with poor T-cell reconstitution after transplantationRoxane Labrosse, Ines Boufaied, Benoîte Bourdin, et al.
Blood|October 13, 2017
Immune reconstitution and survival of 100 SCID patients post-hematopoietic cell transplant: a PIDTC natural history studyJennifer Heimall, Brent R Logan, Morton J Cowan, et al.
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.
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