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The Journal of Allergy and Clinical Immunology|December 2, 2024
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunityGiuliana Giardino, Gigliola Di Matteo, Silvia Giliani, et al.
Journal of Clinical Immunology|April 21, 2022
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)Giuliana Giardino, Cinzia Milito, Vassilios Lougaris, et al.
Human Genetics|June 29, 2021
IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel diseaseMara Cananzi, Elizabeth Wohler, Antonio Marzollo, et al.
Clinical Immunology (Orlando, Fla.)|February 18, 2025
Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopeniaZainab M Golwala, Helena Spiridou Goncalves, Ranjita Devi Moirangthem, et al.
The Journal of Allergy and Clinical Immunology|December 31, 2019
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) scoreVictoria Katharina Tesch, Hassan Abolhassani, Bella Shadur, et al.
The Journal of Experimental Medicine|June 22, 2023
Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patientsAdrian Gervais, Francesca Rovida, Maria Antonietta Avanzini, et al.
The Journal of Allergy and Clinical Immunology|June 30, 2023
Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunityMaria Elena Maccari, Martin Wolkewitz, Charlotte Schwab, et al.
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