Detalhe da pesquisa
1.
The mitochondrial thioredoxin reductase system (TrxR2) in vascular endothelium controls peroxynitrite levels and tissue integrity.
Proc Natl Acad Sci U S A;
118(7)2021 02 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33579817
2.
Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension.
Pediatr Nephrol;
38(7): 2093-2100, 2023 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36538056
3.
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Kidney Int;
100(3): 650-659, 2021 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33940108
4.
Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Pediatr Nephrol;
36(2): 463-471, 2021 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32715379
5.
Blood pressure in children with renal cysts and diabetes syndrome.
Eur J Pediatr;
180(12): 3599-3603, 2021 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34176013
6.
Twelve-month outcome in juvenile proliferative lupus nephritis: results of the German registry study.
Pediatr Nephrol;
35(7): 1235-1246, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32193650
7.
Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.
Pediatr Nephrol;
33(7): 1269-1272, 2018 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29663071
8.
The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.
J Am Soc Nephrol;
28(10): 3066-3075, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28526779
9.
Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.
Pediatr Nephrol;
31(6): 941-55, 2016 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26809805
10.
Correction to: Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Pediatr Nephrol;
36(12): 4015, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34553238
11.
Interleukin-10 enhances recruitment of immune cells in the neonatal mouse model of obstructive nephropathy.
Sci Rep;
14(1): 5495, 2024 03 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38448513
12.
RAGE-mediated interstitial fibrosis in neonatal obstructive nephropathy is independent of NF-κB activation.
Kidney Int;
84(5): 911-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23677242
13.
TLR2 mediates renal apoptosis in neonatal mice subjected experimentally to obstructive nephropathy.
PLoS One;
18(11): e0294142, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38015955
14.
Chronic Kidney Disease in Boys with Posterior Urethral Valves-Pathogenesis, Prognosis and Management.
Biomedicines;
10(8)2022 08 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36009441
15.
Radiation-induced kidney toxicity: molecular and cellular pathogenesis.
Radiat Oncol;
16(1): 43, 2021 Feb 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33632272
16.
Case Report: Pediatric Renal Sarcoidosis and Prognostic Factors in Reviewed Cases.
Front Pediatr;
9: 724728, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34589456
17.
Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic Testing.
Front Genet;
12: 642849, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34122504
18.
Novel heterozygous COL4A3 mutation in a family with late-onset ESRD.
Pediatr Nephrol;
25(8): 1539-42, 2010 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20177710
19.
DAMPs in Unilateral Ureteral Obstruction.
Front Immunol;
11: 581300, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33117389
20.
Homoplasmy of the Mitochondrial DNA Mutation m.616T>C Leads to Mitochondrial Tubulointerstitial Kidney Disease and Encephalopathia.
Nephron;
144(3): 156-160, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31722346