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Clinical Immunology (Orlando, Fla.)|August 30, 2011
Analysis of bulk and virus-specific CD8+ T cells reveals advanced differentiation of CD8+ T cells in patients with common variable immunodeficiencyMartin Kuntz, Sigune Goldacker, Hubert E Blum, et al.Clinical and Experimental Rheumatology|September 1, 2012
Elevated serum osteopontin levels in idiopathic retroperitoneal fibrosisMoritz Binder, Sophie Christoph, Bettina Sehnert, et al.Frontiers in Immunology|December 15, 2025
Do CVID patients on SCIG have more autoimmune (thrombo)cytopenic events than CVID patients on IVIG?Nadezhda Camacho-Ordonez, Aleksandra Hirsch, Luiza Campos, et al.Clinical Immunology (Orlando, Fla.)|November 7, 2025
Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiencyManfred Fliegauf, Kelly Nitschke, Pavla Mrovecova, et al.Molecular Genetics and Metabolism|August 4, 2019
Pegvaliase: Immunological profile and recommendations for the clinical management of hypersensitivity reactions in patients with phenylketonuria treated with this enzyme substitution therapyOliver Hausmann, Mohamed Daha, Nicola Longo, et al.Frontiers in Immunology|March 6, 2023
Lymphoid stromal cells - potential implications for the pathogenesis of CVIDVictoria N Cousin, Guillermo F Perez, Kathryn J Payne, et al.Journal of Clinical Immunology|March 17, 2016
Secondary Antibody Deficiency in Glucocorticoid Therapy Clearly Differs from Primary Antibody DeficiencyClemens Wirsum, Cornelia Glaser, Sylvia Gutenberger, et al.Journal of Clinical Immunology|May 19, 2022
Distinct CD8 T Cell Populations with Differential Exhaustion Profiles Associate with Secondary Complications in Common Variable ImmunodeficiencyAdam Klocperk, David Friedmann, Alexandra Emilia Schlaak, et al.Frontiers in Immunology|July 19, 2019
Corrigendum: Assessing the Functional Relevance of Variants in the IKAROS Family Zinc Finger Protein 1 (IKZF1) in a Cohort of Patients With Primary ImmunodeficiencyZoya Eskandarian, Manfred Fliegauf, Alla Bulashevska, et al.Respiratory Medicine|April 22, 2017
Autosomal dominant gain of function STAT1 mutation and severe bronchiectasisOded Breuer, Hagit Daum, Malena Cohen-Cymberknoh, et al.Pageof 24