Detalhe da pesquisa
1.
Caffeine and kidney function at two years in former extremely low gestational age neonates.
Pediatr Res;
95(1): 257-266, 2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37660176
2.
The Rhesus Macaque Serves As a Model for Human Lateral Branch Nephrogenesis.
J Am Soc Nephrol;
32(5): 1097-1112, 2021 05 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33789950
3.
Under-Recognition of Neonatal Acute Kidney Injury and Lack of Follow-Up.
Am J Perinatol;
39(5): 526-531, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32971562
4.
Omentectomy reduces the need for peritoneal dialysis catheter revision in children: a study from the Pediatric Nephrology Research Consortium.
Pediatr Nephrol;
36(12): 3953-3959, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34128096
5.
Single-Cell Profiling of AKI in a Murine Model Reveals Novel Transcriptional Signatures, Profibrotic Phenotype, and Epithelial-to-Stromal Crosstalk.
J Am Soc Nephrol;
31(12): 2793-2814, 2020 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33115917
6.
Haptoglobin degradation product as a novel serum biomarker for hematopoietic stem cell transplant-associated thrombotic microangiopathy.
Pediatr Nephrol;
34(5): 865-871, 2019 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30569313
7.
Long-term Stability of Urinary Biomarkers of Acute Kidney Injury in Children.
Am J Kidney Dis;
67(1): 56-61, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26032628
8.
Human Nephrogenesis can Persist Beyond 40 Postnatal Days in Preterm Infants.
Kidney Int Rep;
9(2): 436-450, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38344733
9.
Characterizing post-branching nephrogenesis in the neonatal rabbit.
Sci Rep;
13(1): 19234, 2023 11 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37932368
10.
First-Time Use of the Seraph® 100 Microbind® Affinity Blood Filter in an Adolescent Patient with Severe COVID-19 Disease: A Case Report.
Case Rep Nephrol Dial;
13(1): 1-6, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36741548
11.
Regulation of nephron progenitor cell lifespan and nephron endowment.
Nat Rev Nephrol;
18(11): 683-695, 2022 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36104510
12.
Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary Tract.
Front Pediatr;
10: 898773, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35990004
13.
Disarranged Sphingolipid Metabolism From Sphingosine-1-Phosphate Lyase Deficiency Leads to Congenital Nephrotic Syndrome.
Kidney Int Rep;
4(12): 1763-1769, 2019 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31844815