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Edwin Kwan Soon Wong
Edwin Kwan Soon Wong
Verified email at newcastle.ac.uk - Homepage
Title
Cited by
Cited by
Year
Hemolytic uremic syndrome in pregnancy and postpartum
A Bruel, D Kavanagh, M Noris, Y Delmas, EKS Wong, E Bresin, F Provôt, ...
Clinical Journal of the American Society of Nephrology 12 (8), 1237-1247, 2017
2112017
The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment
E Rondeau, M Scully, G Ariceta, T Barbour, S Cataland, N Heyne, ...
Kidney international 97 (6), 1287-1296, 2020
1502020
Diseases of complement dysregulation—an overview
EKS Wong, D Kavanagh
Seminars in immunopathology 40 (1), 49-64, 2018
1192018
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration
Y Yu, MP Triebwasser, EKS Wong, EC Schramm, B Thomas, R Reynolds, ...
Human molecular genetics 23 (19), 5283-5293, 2014
1192014
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
EKS Wong, THJ Goodship, D Kavanagh
Molecular immunology 56 (3), 199-212, 2013
1042013
Anticomplement C5 therapy with eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome
EKS Wong, D Kavanagh
Translational Research 165 (2), 306-320, 2015
902015
An extended mini-complement factor H molecule ameliorates experimental C3 glomerulopathy
EM Nichols, TD Barbour, IY Pappworth, EKS Wong, JM Palmer, ...
Kidney international 88 (6), 1314-1322, 2015
762015
Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland
V Brocklebank, S Johnson, TP Sheerin, SD Marks, RD Gilbert, K Tyerman, ...
Kidney international 92 (5), 1261-1271, 2017
692017
Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data
JHR Farmery, ML Smith, AG Lynch
Scientific reports 8 (1), 1300, 2018
652018
The role of ADAMTS‐13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies
EH Phillips, JP Westwood, V Brocklebank, EKS Wong, JO Tellez, ...
Journal of Thrombosis and Haemostasis 14 (1), 175-185, 2016
562016
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN
EKS Wong, HE Anderson, AP Herbert, RC Challis, P Brown, GS Reis, ...
Journal of the American Society of Nephrology 25 (11), 2425-2433, 2014
532014
Thrombotic microangiopathy in inverted formin 2–mediated renal disease
RC Challis, T Ring, Y Xu, EKS Wong, O Flossmann, ISD Roberts, ...
Journal of the American Society of Nephrology 28 (4), 1084-1091, 2017
522017
A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H–Related 3 Gene in Atypical Hemolytic Uremic …
RC Challis, GSR Araujo, EKS Wong, HE Anderson, A Awan, AM Dorman, ...
Journal of the American Society of Nephrology 27 (6), 1617-1624, 2016
502016
Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy
V Brocklebank, G Kumar, AJ Howie, J Chandar, DV Milford, J Craze, ...
Kidney international 97 (6), 1260-1274, 2020
382020
Long-term efficacy and safety of the long-acting complement C5 inhibitor ravulizumab for the treatment of atypical hemolytic uremic syndrome in adults
T Barbour, M Scully, G Ariceta, S Cataland, K Garlo, N Heyne, Y Luque, ...
Kidney international reports 6 (6), 1603-1613, 2021
362021
Large-scale whole-genome sequencing reveals the genetic architecture of primary membranoproliferative GN and C3 glomerulopathy
AP Levine, MMY Chan, O Sadeghi-Alavijeh, EKS Wong, HT Cook, ...
Journal of the American Society of Nephrology 31 (2), 365-373, 2020
352020
Disease-linked mutations in factor H reveal pivotal role of cofactor activity in Self-surface–selective regulation of complement activation
H Kerr, E Wong, E Makou, Y Yang, K Marchbank, D Kavanagh, ...
Journal of Biological Chemistry 292 (32), 13345-13360, 2017
302017
C3 glomerulopathy and related disorders in children: etiology-phenotype correlation and outcomes
EKS Wong, KJ Marchbank, H Lomax-Browne, IY Pappworth, H Denton, ...
Clinical Journal of the American Society of Nephrology 16 (11), 1639-1651, 2021
182021
Functional characterization of rare genetic variants in the N-terminus of complement factor H in aHUS, C3G, and AMD
EKS Wong, TM Hallam, V Brocklebank, PR Walsh, K Smith-Jackson, ...
Frontiers in immunology 11, 602284, 2021
172021
Atypical haemolytic uraemic syndrome associated with a CD46 mutation triggered by Shigella flexneri
V Brocklebank, EKS Wong, R Fielding, THJ Goodship, D Kavanagh
Clinical kidney journal 7 (3), 286-288, 2014
172014
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