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Clinical and Experimental Immunology|July 8, 2021
Newborn screening for severe combined immunodeficiency-Coming to a region near you soonDavid A C Elliman, Andrew R GenneryDNA Repair|March 18, 2014
The clinical impact of deficiency in DNA non-homologous end-joiningLisa Woodbine, Andrew R Gennery, Penny A JeggoFrontiers in Immunology|November 29, 2023
Too much of a good thing: a review of primary immune regulatory disordersChristo Tsilifis, Mary A Slatter, Andrew R GenneryJournal of Clinical Immunology|May 1, 2021
STAT3 Hyper-IgE Syndrome-an Update and Unanswered QuestionsChristo Tsilifis, Alexandra F Freeman, Andrew R GenneryDNA Repair|May 1, 2014
Reprint of "The clinical impact of deficiency in DNA non-homologous end-joining"Lisa Woodbine, Andrew R Gennery, Penny A JeggoFrontiers in Pediatrics|July 5, 2017
Infusion of Sibling Marrow in a Patient with Purine Nucleoside Phosphorylase Deficiency Leads to Split Mixed Donor Chimerism and Normal ImmunityLaura Yeates, Mary A Slatter, Andrew R GenneryThe Journal of Allergy and Clinical Immunology|March 15, 2020
Neonatal thymectomy in children-accelerating the immunologic clock?Angela Deya-Martinez, Aisling M Flinn, Andrew R GenneryCurrent Opinion in Allergy and Clinical Immunology|October 31, 2024
Update on hereditary C1q deficiency: pathophysiology, clinical presentation, genotype and managementHelena Buso, Clément Triaille, Aisling M Flinn, et al.Journal of Clinical Immunology|August 24, 2023
Allogeneic HSCT for Symptomatic Female X-linked Chronic Granulomatous Disease CarriersChristo Tsilifis, Tuulia Torppa, Eleri J Williams, et al.The Journal of Allergy and Clinical Immunology|May 20, 2008
Immunologic defects in 22q11.2 deletion syndromeAndrew McLean-Tooke, Dawn Barge, Gavin P Spickett, et al.Pageof 35