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American Journal of Respiratory and Critical Care Medicine|July 10, 2012
Spatial clusters of nontuberculous mycobacterial lung disease in the United StatesJennifer Adjemian, Kenneth N Olivier, Amy E Seitz, et al.The Journal of Clinical Investigation|July 24, 2018
TNF overproduction impairs epithelial staphylococcal response in hyper IgE syndromeIan A Myles, Erik D Anderson, Noah J Earland, et al.The New England Journal of Medicine|March 20, 2024
Anti-Interleukin-23 Autoantibodies in Adult-Onset ImmunodeficiencyAristine Cheng, Anuj Kashyap, Helene Salvator, et al.The Journal of Allergy and Clinical Immunology|December 1, 2023
GenIA, the Genetic Immunology Advisor database for inborn errors of immunityAndrés Caballero-Oteyza, Laura Crisponi, Xiao P Peng, et al.BMC Research Notes|February 2, 2011
Novel human genetic variants associated with extrapulmonary tuberculosis: a pilot genome wide association studyNoffisat O Oki, Alison A Motsinger-Reif, Paulo Rz Antas, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 13, 2005
Posaconazole as salvage therapy in patients with chronic granulomatous disease and invasive filamentous fungal infectionBrahm H Segal, Lisa A Barnhart, Victoria L Anderson, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|June 4, 2013
MonoMAC syndrome in a patient with a GATA2 mutation: case report and review of the literatureJose F Camargo, Stephen A Lobo, Amy P Hsu, et al.Frontiers in Genetics|March 14, 2022
ARZIMM: A Novel Analytic Platform for the Inference of Microbial Interactions and Community Stability from Longitudinal Microbiome StudyLinchen He, Chan Wang, Jiyuan Hu, et al.Journal of Clinical Immunology|May 3, 2013
Molecular identification of bacterial DNA in the chorioretinal scars of chronic granulomatous diseaseYujuan Wang, Beatriz E Marciano, Defen Shen, et al.Journal of Clinical Immunology|April 1, 2014
Correlating interleukin-12 stimulated interferon-γ production and the absence of ectodermal dysplasia and anhidrosis (EDA) in patients with mutations in NF-κB essential modulator (NEMO)Margje H Haverkamp, Beatriz E Marciano, David M Frucht, et al.Pageof 68