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1.
Atypical hemolytic uremic syndrome in the era of terminal complement inhibition: an observational cohort study.
Blood
; 142(16): 1371-1386, 2023 10 19.
Article
in English
| MEDLINE | ID: mdl-37369098
2.
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy.
J Am Soc Nephrol
; 31(2): 365-373, 2020 02.
Article
in English
| MEDLINE | ID: mdl-31919107
3.
Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy.
Kidney Int
; 97(6): 1260-1274, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32386968
4.
Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.
J Am Soc Nephrol
; 28(4): 1084-1091, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-27974406
5.
Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland.
Kidney Int
; 92(5): 1261-1271, 2017 11.
Article
in English
| MEDLINE | ID: mdl-28750931
6.
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 Syndrome.
J Am Soc Nephrol
; 27(6): 1617-24, 2016 06.
Article
in English
| MEDLINE | ID: mdl-26490391
7.
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration.
Hum Mol Genet
; 23(19): 5283-93, 2014 Oct 01.
Article
in English
| MEDLINE | ID: mdl-24847005
8.
An extended mini-complement factor H molecule ameliorates experimental C3 glomerulopathy.
Kidney Int
; 88(6): 1314-1322, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26221753
9.
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.
J Am Soc Nephrol
; 25(11): 2425-33, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-24722444
10.
Making sense of the spectrum of glomerular disease associated with complement dysregulation.
Pediatr Nephrol
; 29(10): 1883-94, 2014 Oct.
Article
in English
| MEDLINE | ID: mdl-23852337
11.
Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome.
Transplantation
; 107(4): 994-1003, 2023 04 01.
Article
in English
| MEDLINE | ID: mdl-36413152
12.
A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative CFI variants in age-related macular degeneration.
Front Immunol
; 13: 1028760, 2022.
Article
in English
| MEDLINE | ID: mdl-36643920
13.
C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and Outcomes.
Clin J Am Soc Nephrol
; 16(11): 1639-1651, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34551983
14.
Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD.
Front Immunol
; 11: 602284, 2020.
Article
in English
| MEDLINE | ID: mdl-33519811
15.
Diseases of complement dysregulation-an overview.
Semin Immunopathol
; 40(1): 49-64, 2018 01.
Article
in English
| MEDLINE | ID: mdl-29327071
16.
Hemolytic Uremic Syndrome in Pregnancy and Postpartum.
Clin J Am Soc Nephrol
; 12(8): 1237-1247, 2017 Aug 07.
Article
in English
| MEDLINE | ID: mdl-28596415
17.
Anticomplement C5 therapy with eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome.
Transl Res
; 165(2): 306-20, 2015 Feb.
Article
in English
| MEDLINE | ID: mdl-25468487
18.
Sarcoidosis presenting with hypercalcaemia following withdrawal of long-term immunosuppression in renal transplantation.
Oxf Med Case Reports
; 2014(5): 86-8, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-25988038
19.
Atypical haemolytic uraemic syndrome associated with a CD46 mutation triggered by Shigella flexneri.
Clin Kidney J
; 7(3): 286-288, 2014 Jun.
Article
in English
| MEDLINE | ID: mdl-24944786
20.
Complement therapy in atypical haemolytic uraemic syndrome (aHUS).
Mol Immunol
; 56(3): 199-212, 2013 Dec 15.
Article
in English
| MEDLINE | ID: mdl-23810412