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Frontiers in Immunology|August 4, 2017
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
The Journal of Allergy and Clinical Immunology|November 7, 2023
JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective studyMarco Fischer, Peter Olbrich, Jérôme Hadjadj, et al.
The Journal of Allergy and Clinical Immunology|January 21, 2019
Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC studyFrancesca Ferrua, Stefania Galimberti, Virginie Courteille, et al.
The Journal of Clinical Investigation|July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous diseaseAnnemarie van de Geer, Alejandro Nieto-Patlán, Douglas B Kuhns, et al.
Bone Marrow Transplantation|July 10, 2026
Timing is everything: outcomes of allogeneic HSCT in adults with inborn errors of immunityKatharine Orf, Hannah Al Yousuf, Thomas A Fox, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 17, 2019
Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG DeficiencyJocelyn R Farmer, Zsofia Foldvari, Boglarka Ujhazi, et al.
Science Immunology|January 10, 2025
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signatureMarita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, et al.
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