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Author/Creator Grainger, Angela

2. A Novel Case of Homozygous Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency With Hemophagocytic Lymphohistiocytosis. (30th November 2020)

Authors:
Gothe, Florian; Hatton, Catherine F; Truong, Linh; Klimova, Zofia; Kanderova, Veronika; Fejtkova, Martina; Grainger, Angela; Bigley, Venetia; Perthen, Joanna; Mitra, Dipayan; Janda, Ales; Fronkova, Eva; Moravcikova, Dusana; Hambleton, Sophie; Duncan, Christopher J A
Journal:
Clinical infectious diseases
Issue:
Volume 74:Number 1(2022)
Page Start:
136
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20). Issue 5 (28th June 2017)

Authors:
Duncan, Christopher J A; Dinnigan, Emma; Theobald, Rachel; Grainger, Angela; Skelton, Andrew J; Hussain, Rafiqul; Willet, Joseph D P; Swan, David J; Coxhead, Jonathan; Thomas, Matthew F; Thomas, Julian; Zamvar, Veena; Slatter, Mary A; Cant, Andrew J; Engelhardt, Karin R; Hambleton, Sophie
Journal:
Annals of the rheumatic diseases
Issue:
Volume 77:Issue 5(2018)
Page Start:
783
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗