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Clinical Immunology (Orlando, Fla.)|August 4, 2018
Deficiencies in the CD19 complexMarjolein W J Wentink, Menno C van Zelm, Jacques J M van Dongen, et al.Journal of Neurology|July 1, 2021
Pembrolizumab for treatment of progressive multifocal leukoencephalopathy in primary immunodeficiency and/or hematologic malignancy: a case series of five patientsTimo Volk, Klaus Warnatz, Reinhard Marks, et al.Frontiers in Immunology|May 7, 2019
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.The Journal of Experimental Medicine|April 12, 2018
Germline deletion of CIN85 in humans with X chromosome-linked antibody deficiencyBaerbel Keller, Moneef Shoukier, Kathrin Schulz, et al.Proceedings of the National Academy of Sciences of the United States of America|February 8, 2022
Autoreactive antibodies control blood glucose by regulating insulin homeostasisTimm Amendt, Gabriele Allies, Antonella Nicolò, et al.Blood|February 28, 2002
Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous diseaseKlaus Warnatz, Axel Denz, Ruth Dräger, et al.Immunology Letters|March 29, 2025
BENTA disease or CARD11 gain-of-function? A novel variant with atypical features and a literature reviewLetizia Baldini, Bärbel Keller, Lisa Dewitte, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 25, 2010
B cell receptor-mediated calcium signaling is impaired in B lymphocytes of type Ia patients with common variable immunodeficiencyChristian Foerster, Nadine Voelxen, Mirzokhid Rakhmanov, et al.Plos One|May 26, 2012
Impact of rituximab on immunoglobulin concentrations and B cell numbers after cyclophosphamide treatment in patients with ANCA-associated vasculitidesNils Venhoff, Nora M Effelsberg, Ulrich Salzer, et al.Zeitschrift Fur Rheumatologie|February 3, 2023
[Macrocytic anemia and polychondritis: VEXAS syndrome]Markus Zeisbrich, Viktoria Schindler, Máté Krausz, et al.Pageof 24