Detalhe da pesquisa
1.
Red blood cell-derived arginase release in hemolytic uremic syndrome.
J Transl Med
; 22(1): 17, 2024 Jan 04.
Artigo
Inglês
| MEDLINE | ID: mdl-38178089
2.
Complement dysregulation associated with a genetic variant in factor H-related protein 5 in atypical hemolytic uremic syndrome.
Pediatr Nephrol
; 39(4): 1105-1111, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-37955705
3.
A link between Krüppel-like factor 4, complement activation, and kidney damage.
Kidney Int
; 102(1): 14-16, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35738827
4.
In Vivo Sustained Release of the Retrograde Transport Inhibitor Retro-2.1 Formulated in a Thermosensitive Hydrogel.
Int J Mol Sci
; 23(23)2022 Nov 23.
Artigo
Inglês
| MEDLINE | ID: mdl-36498939
5.
Exosomes and microvesicles in normal physiology, pathophysiology, and renal diseases.
Pediatr Nephrol
; 34(1): 11-30, 2019 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29181712
6.
Aliskiren inhibits renin-mediated complement activation.
Kidney Int
; 94(4): 689-700, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-29884545
7.
Early Terminal Complement Blockade and C6 Deficiency Are Protective in Enterohemorrhagic Escherichia coli-Infected Mice.
J Immunol
; 197(4): 1276-86, 2016 08 15.
Artigo
Inglês
| MEDLINE | ID: mdl-27421478
8.
C1-Inhibitor Decreases the Release of Vasculitis-Like Chemotactic Endothelial Microvesicles.
J Am Soc Nephrol
; 28(8): 2472-2481, 2017 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-28289183
9.
Microvesicle transfer of kinin B1-receptors is a novel inflammatory mechanism in vasculitis.
Kidney Int
; 91(1): 96-105, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27914700
10.
Haemolytic uraemic syndrome.
J Intern Med
; 281(2): 123-148, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27723152
11.
A novel mechanism of bacterial toxin transfer within host blood cell-derived microvesicles.
PLoS Pathog
; 11(2): e1004619, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25719452
12.
Shiga toxin-induced complement-mediated hemolysis and release of complement-coated red blood cell-derived microvesicles in hemolytic uremic syndrome.
J Immunol
; 194(5): 2309-18, 2015 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-25637016
13.
Orphan drug policies and use in pediatric nephrology.
Pediatr Nephrol
; 32(1): 1-6, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27738765
14.
Complement contributes to the pathogenesis of Shiga toxin-associated hemolytic uremic syndrome.
Kidney Int
; 90(4): 726-9, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27633864
15.
The combined role of galactose-deficient IgA1 and streptococcal IgA-binding M Protein in inducing IL-6 and C3 secretion from human mesangial cells: implications for IgA nephropathy.
J Immunol
; 193(1): 317-26, 2014 Jul 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24850720
16.
An international consensus approach to the management of atypical hemolytic uremic syndrome in children.
Pediatr Nephrol
; 31(1): 15-39, 2016 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25859752
17.
Complement activation associated with ADAMTS13 deficiency in human and murine thrombotic microangiopathy.
J Immunol
; 191(5): 2184-93, 2013 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23878316
18.
Complement Interactions with Blood Cells, Endothelial Cells and Microvesicles in Thrombotic and Inflammatory Conditions.
Adv Exp Med Biol
; 865: 19-42, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26306441
19.
A novel C3 mutation causing increased formation of the C3 convertase in familial atypical hemolytic uremic syndrome.
J Immunol
; 188(4): 2030-7, 2012 Feb 15.
Artigo
Inglês
| MEDLINE | ID: mdl-22250080
20.
Eculizumab treatment for rescue of renal function in IgA nephropathy.
Pediatr Nephrol
; 29(11): 2225-8, 2014 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-24924752