Showing results (21-30 of 99) with videos related to
Sort By:
Pageof 10
Frontiers in Immunology|November 23, 2020
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic RhinitisBianca Cinicola, Andrea Uva, Lucia Leonardi, et al.Frontiers in Immunology|September 20, 2024
Corrigendum: Abnormalities of thymic stroma may contribute to immune dysregulation in murine models of leaky severe combined immunodeficiencyFrancesca Rucci, Pietro Luigi Poliani, Stefano Caraffi, et al.Current Drug Metabolism|November 4, 2015
Patients' Induced Pluripotent Stem Cells to Model Drug Induced Adverse Events: A Role in Predicting Thiopurine Induced Pancreatitis?Gabriele Stocco, Gaetana Lanzi, Fengming Yue, et al.Blood|February 5, 2010
Impaired NK-cell migration in WAS/XLT patients: role of Cdc42/WASp pathway in the control of chemokine-induced beta2 integrin high-affinity stateHelena Stabile, Claudia Carlino, Cinzia Mazza, et al.Blood|March 6, 2004
Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defectAngela Gismondi, Loredana Cifaldi, Cinzia Mazza, et al.Vaccines|November 21, 2019
Persistent Infection with Rotavirus Vaccine Strain in Severe Combined Immunodeficiency (SCID) Child: Is Rotavirus Vaccination in SCID Children a Janus Face?Maria Antonia De Francesco, Giovanni Ianiro, Marina Monini, et al.Virology Journal|November 16, 2012
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy childrenSusanna Esposito, Claudio Giuseppe Molteni, Silvia Giliani, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 22, 2008
Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patientsAlessandra Pangrazio, Maria Elena Caldana, Cristina Sobacchi, et al.European Journal of Pediatrics|September 17, 2004
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndromeClaudia Fiorini, Sawssen Jilani, Claretta Gioia Losi, et al.Immunologic Research|July 2, 2008
Single-center analysis of long-term outcome after hematopoietic cell transplantation in children with congenital severe T cell immunodeficiencyEvelina Mazzolari, Donatella de Martiis, Concetta Forino, et al.Pageof 10