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Blood|July 21, 2011
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutationDonatella Vairo, Laura Tassone, Giovanna Tabellini, et al.Advances in Immunology|May 10, 2006
Immunodeficiencies with autoimmune consequencesLuigi D Notarangelo, Eleonora Gambineri, Raffaele BadolatoImmunobiology|April 22, 2023
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasisManuela Baronio, Luisa Gazzurelli, Sara Rezzola, et al.Immunological Reviews|January 22, 2005
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological featuresVassilios Lougaris, Raffaele Badolato, Simona Ferrari, et al.Expert Review of Clinical Immunology|December 20, 2019
Novel and emerging treatments for Aicardi-Goutières syndromeDavide Tonduti, Elisa Fazzi, Raffaele Badolato, et al.Current Opinion in Allergy and Clinical Immunology|January 11, 2005
Congenital neutropenia: advances in diagnosis and treatmentRaffaele Badolato, Stefania Fontana, Lucia D Notarangelo, et al.Plos One|December 5, 2013
Occurrence of nodular lymphocyte-predominant hodgkin lymphoma in hermansky-pudlak type 2 syndrome is associated to natural killer and natural killer T cell defectsLuisa Lorenzi, Giovanna Tabellini, William Vermi, et al.Journal of Leukocyte Biology|November 3, 2016
STAT mutations as program switchers: turning primary immunodeficiencies into autoimmune diseasesTiziana Lorenzini, Laura Dotta, Mauro Giacomelli, et al.The Journal of Allergy and Clinical Immunology|January 11, 2017
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutationsGiovanna Tabellini, Donatella Vairo, Omar Scomodon, et al.Current Opinion in Pediatrics|September 16, 2017
Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disordersFilippo Consonni, Laura Dotta, Francesca Todaro, et al.Pageof 19