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International Journal of Neonatal Screening|January 25, 2022
Flow Cytometry Confirmation Post Newborn Screening for SCID in EnglandKimberly C Gilmour
Expert Review of Molecular Diagnostics|September 27, 2003
Pathogenesis and diagnosis of X-linked lymphoproliferative diseaseKimberly C Gilmour, H Bobby Gaspar
The Journal of Pediatrics|May 11, 2013
22q11.2 deletion syndrome with life-threatening adenovirus infectionWinnie Ip, Hong Zhan, Kimberly C Gilmour, et al.
F1000Research|January 15, 2021
'The long tail of Covid-19' - The detection of a prolonged inflammatory response after a SARS-CoV-2 infection in asymptomatic and mildly affected patientsIvan Doykov, Jenny Hällqvist, Kimberly C Gilmour, et al.
Ejhaem|August 19, 2024
Case series: Congenital enterovirus infection-associated haemophagocytic lymphohistiocytosis and subsequent neutropaeniaJustin Penner, James E Burns, Judith Breuer, et al.
The Journal of Pediatrics|July 14, 2022
High Prevalence of Hemophagocytic Lymphohistiocytosis in Acute Liver Failure of InfancyNedim Hadžić, Emese Molnar, Sue Height, et al.
Blood Advances|January 4, 2018
Cord blood transplantation recapitulates fetal ontogeny with a distinct molecular signature that supports CD4+ T-cell reconstitutionPrashant Hiwarkar, Mike Hubank, Waseem Qasim, et al.
Blood|January 17, 2004
SAP mediates specific cytotoxic T-cell functions in X-linked lymphoproliferative diseaseReza Sharifi, Joanna C Sinclair, Kimberly C Gilmour, et al.
Oncoimmunology|September 14, 2016
Missense mutations in the perforin (PRF1) gene as a cause of hereditary cancer predispositionMohammed S Chaudhry, Kimberly C Gilmour, Imran G House, et al.
Frontiers in Immunology|June 28, 2023
Combined novel homozygous variants in both SGPL1 and STAT1 presenting with severe combined immune deficiency: case report and literature reviewAdriel Roa-Bautista, Mahreen Sohail, Emma Wakeling, et al.
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