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Journal of Clinical Immunology|March 26, 2022
Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 DeficiencyJérémie Rosain, Andrea Bernasconi, Emma Prieto, et al.
Journal of Clinical Immunology|February 16, 2024
Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ DeficiencyJérémie Rosain, Ayca Kiykim, Alexandre Michev, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 23, 2024
A sensitive assay for measuring whole-blood responses to type I IFNsAdrian Gervais, Corentin Le Floc'h, Tom Le Voyer, et al.
The New England Journal of Medicine|January 16, 2020
JAK Inhibitor Therapy in a Child with Inherited USP18 DeficiencyFahad Alsohime, Marta Martin-Fernandez, Mohamad-Hani Temsah, et al.
Journal of Clinical Immunology|March 29, 2018
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi ArabiaAbdulrahman N Alodayani, Abdulnasir M Al-Otaibi, Caroline Deswarte, et al.
The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
Ebiomedicine|December 19, 2022
Inflammatory markers and auto-Abs to type I IFNs in COVID-19 convalescent plasma cohort studyFabrice Cognasse, Hind Hamzeh-Cognasse, Mickael Rosa, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 4, 2024
Inherited human RelB deficiency impairs innate and adaptive immunity to infectionTom Le Voyer, Majistor Raj Luxman Maglorius Renkilaraj, Kunihiko Moriya, 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.
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