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Blood|January 16, 2024
Antinuclear antibody-associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosusJérôme Granel, Helder Fernandes, Brigitte Bader-Meunier, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exonsAlexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Blood|January 9, 2024
Clinical and functional spectrum of RAC2-related immunodeficiencyÁgnes Donkó, Svetlana O Sharapova, Juraj Kabat, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 5, 2018
Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 DeficiencySusanne E Aydin, Alexandra F Freeman, Waleed Al-Herz, 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.
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|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 Experimental Medicine|November 22, 2024
Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C)Evangelos Bellos, Dilys Santillo, Pierre Vantourout, et al.
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