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Science (New York, N.Y.)|July 15, 2020
Impaired type I interferon activity and inflammatory responses in severe COVID-19 patientsJérôme Hadjadj, Nader Yatim, Laura Barnabei, et al.Lancet (London, England)|October 29, 2013
Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre studyTayfun Güngör, Pierre Teira, Mary Slatter, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 25, 2011
Insertion sites in engrafted cells cluster within a limited repertoire of genomic areas after gammaretroviral vector gene therapyAnnette Deichmann, Martijn H Brugman, Cynthia C Bartholomae, et al.Journal of Human Immunity|December 5, 2025
Inborn errors of immunity: Manifestation, treatment, and outcome-an ESID registry 1994-2024 report on 30,628 patientsGerhard Kindle, Mickaël Alligon, Michael H Albert, et al.Nature|March 21, 2024
Role of IL-27 in Epstein-Barr virus infection revealed by IL-27RA deficiencyEmmanuel Martin, Sarah Winter, Cécile Garcin, et al.Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
Inborn errors of immunity: manifestation, treatment, and outcome - an ESID registry 1994-2024 report on 30,628 patientsGerhard Kindle, Mickaël Alligon, Michael H Albert, et al.The Journal of Clinical Investigation|December 8, 2020
Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiencyBethany A Pillay, Mathieu Fusaro, Paul E Gray, et al.Journal of Clinical Immunology|November 5, 2025
Consecutive non-Aspergillus Fungal Invasive Infections in Chronic Granulomatous Disease: Data from the French National Reference Center for Primary ImmunoDeficiencies and literature reviewLeïla Lefevre, Olivier Paccoud, Bénédicte Neven, et al.The Journal of Allergy and Clinical Immunology|October 4, 2023
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndromeOlivier Pellé, Solange Moreno, Myriam Ricarda Lorenz, et al.Blood|December 2, 2010
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, et al.Pageof 44