Detalhe da pesquisa
1.
Mutations in atypical hemolytic uremic syndrome provide evidence for the role of calcium in complement factor I.
Blood
; 142(6): 607-610, 2023 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37363824
2.
Functional analysis of rare genetic variants in complement factor I in advanced age-related macular degeneration.
Hum Mol Genet
; 31(21): 3683-3693, 2022 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35531992
3.
Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study.
BJOG
; 130(12): 1473-1482, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37156755
4.
A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor H.
J Am Soc Nephrol
; 27(6): 1665-77, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26471127
5.
Defective complement inhibitory function predisposes to renal disease.
Annu Rev Med
; 64: 307-24, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23121180
6.
Cytomegalovirus-induced thrombotic microangiopathy after renal transplant successfully treated with eculizumab: case report and review of the literature.
Transpl Int
; 28(9): 1121-5, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25864519
7.
Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia.
Res Sq
; 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38645143
8.
Show Me CKDintercept Initiative: A Collective Impact Approach to Improve Population Health in Missouri.
Mayo Clin Proc Innov Qual Outcomes
; 8(1): 82-96, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38283097
9.
The Role of Complement in Autoimmune Disease-Associated Thrombotic Microangiopathy and the Potential for Therapeutics.
J Rheumatol
; 50(6): 730-740, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36642429
10.
Rare Dysfunctional Complement Factor I Genetic Variants and Progression to Advanced Age-Related Macular Degeneration.
Ophthalmol Sci
; 3(2): 100265, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36909148
11.
Treatment preference and quality of life impact: ravulizumab vs eculizumab for atypical hemolytic uremic syndrome.
J Comp Eff Res
; 12(9): e230036, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37515502
12.
De novo membranoproliferative glomerulonephritis III in a renal transplant patient: case report and review of the literature.
Transpl Int
; 25(5): e58-61, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22380572
13.
Post-Transplant Thrombotic Microangiopathy due to a Pathogenic Mutation in Complement Factor I in a Patient With Membranous Nephropathy: Case Report and Review of Literature.
Front Immunol
; 13: 909503, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35720299
14.
Differentiating Hemolysis, Elevated Liver Enzymes, and Low Platelet Count Syndrome and Atypical Hemolytic Uremic Syndrome in the Postpartum Period.
Hypertension
; 78(3): 760-768, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34275337
15.
Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation.
Front Med (Lausanne)
; 8: 775280, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34912830
16.
Peri- and Post-operative Evaluation and Management of Atypical Hemolytic Uremic Syndrome (aHUS) in Kidney Transplantation.
Adv Chronic Kidney Dis
; 27(2): 128-137, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32553245
17.
Functional Analysis of Rare Genetic Variants in Complement Factor I (CFI) using a Serum-Based Assay in Advanced Age-related Macular Degeneration.
Transl Vis Sci Technol
; 9(9): 37, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32908800
18.
The complement system in COVID-19: friend and foe?
JCI Insight
; 5(15)2020 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32554923
19.
Complement Dysregulation and Disease: Insights from Contemporary Genetics.
Annu Rev Pathol
; 12: 25-52, 2017 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27959629
20.
Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD.
Sci Rep
; 6: 31531, 2016 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27572114