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International Journal of Hematology|May 3, 2024
Highly sensitive detection of Epstein-Barr virus-infected cells by EBER flow FISHDan Tomomasa, Kay Tanita, Yuriko Hiruma, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 20, 2023
Chronic Aichi Virus Infection As a Cause of Long-Lasting Multiorgan Involvement in Patients With Primary Immune DeficienciesJacques Fourgeaud, Mathilde M Lecuit, Philippe Pérot, et al.Rheumatology (Oxford, England)|May 24, 2025
Myositis-specific autoantibody subtypes are associated with response to Janus kinase inhibitors in patients with juvenile dermatomyositisBrigitte Bader-Meunier, Thomas R J Moreau, Florence Aeschlimann, et al.Journal of Clinical Immunology|February 3, 2021
Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and MalformationsMathieu Fusaro, Aline Vincent, Martin Castelle, et al.Blood Advances|December 17, 2021
Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulationTala Shahin, Daniel Mayr, Mohamed R Shoeb, 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.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.Nature Communications|June 22, 2023
NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cellsLaure Delage, Francesco Carbone, Quentin Riller, et al.The Journal of Clinical Investigation|June 12, 2018
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiencyDavid Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, et al.Pageof 15