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Transfusion Medicine (Oxford, England)|June 23, 2026
Implementation of BSH 2020 irradiation guidelines for children with DiGeorge syndromeOliver Firth, Philip Arnold, Andrew R Gennery, et al.The Journal of Experimental Medicine|January 20, 2005
Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cellsQiang Pan-Hammarström, Anne-Marie Jones, Aleksi Lähdesmäki, et al.Journal of Evaluation in Clinical Practice|October 15, 2013
Changing clinical practice: management of paediatric community-acquired pneumoniaMohamed A Elemraid, Stephen P Rushton, Matthew F Thomas, et al.Blood|January 29, 2011
Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screeningLucinda Brown, Jinhua Xu-Bayford, Zoe Allwood, et al.Journal of Clinical Immunology|March 15, 2019
Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United KingdomAlexandra C Battersby, Helen Braggins, Mark S Pearce, et al.Neuropediatrics|February 12, 2013
Cognitive ability in children with chronic granulomatous disease: a comparison of those managed conservatively with those who have undergone hematopoietic stem cell transplantTheresa S Cole, Fiona McKendrick, Andrew J Cant, et al.The Journal of Experimental Medicine|December 17, 2008
Involvement of Artemis in nonhomologous end-joining during immunoglobulin class switch recombinationLikun Du, Mirjam van der Burg, Sergey W Popov, et al.Metabolomics : Official Journal of the Metabolomic Society|September 26, 2025
OMNImet®•GUT collection kit supports sample collection and ambient temperature preservation of faecal short chain fatty acidsJemma Cleminson, Caroline Kerbiriou, Shona McKirdy, et al.The Journal of Allergy and Clinical Immunology|August 3, 2010
Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: entering a new century, do we do better?Andrew R Gennery, Mary A Slatter, Laure Grandin, et al.Clinical Immunology (Orlando, Fla.)|June 19, 2007
GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genesIram J Haq, Laura J Steinberg, Manfred Hoenig, et al.Pageof 25