Detalhe da pesquisa
1.
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.
Pediatr Nephrol
; 39(6): 1847-1858, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38196016
2.
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.
Kidney Int
; 103(5): 962-972, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36898413
3.
Clinical and genetic characteristics of Dent's disease type 1 in Europe.
Nephrol Dial Transplant
; 38(6): 1497-1507, 2023 05 31.
Artigo
Inglês
| MEDLINE | ID: mdl-36441012
4.
Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression.
Pediatr Nephrol
; 38(5): 1499-1511, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36315273
5.
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Kidney Int
; 102(3): 604-612, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35643375
6.
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Kidney Int
; 102(3): 592-603, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35483523
7.
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
Inglês
| MEDLINE | ID: mdl-33940108
8.
The European Society for Paediatric Nephrology study of pediatric renal care in Europe: comparative analysis 1998-2017.
Pediatr Nephrol
; 35(1): 103-111, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31664556
9.
Corrigendum to "A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants." Kidney Int. 2023;103:962-972.
Kidney Int
; 105(1): 213-214, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38182294
10.
CTNS mRNA molecular analysis revealed a novel mutation in a child with infantile nephropathic cystinosis: a case report.
BMC Nephrol
; 20(1): 400, 2019 10 31.
Artigo
Inglês
| MEDLINE | ID: mdl-31672123
11.
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease.
J Pediatr
; 199: 22-28.e6, 2018 08.
Artigo
Inglês
| MEDLINE | ID: mdl-29753540
12.
Capacity for the management of kidney failure in the International Society of Nephrology Newly Independent States and Russia region: report from the 2023 ISN Global Kidney Health Atlas (ISN-GKHA).
Kidney Int Suppl (2011)
; 13(1): 71-82, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38618496
13.
Diversity of kidney care referral pathways in national child health systems of 48 European countries.
Front Pediatr
; 12: 1327422, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38292210
14.
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium.
Kidney Int Rep
; 8(10): 2029-2042, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37849991
15.
Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry.
Kidney Int Rep
; 7(7): 1608-1618, 2022 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-35812297
16.
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease.
Kidney Int Rep
; 7(7): 1643-1652, 2022 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-35812281
17.
Long-Term Transplantation Outcomes in Patients With Primary Hyperoxaluria Type 1 Included in the European Hyperoxaluria Consortium (OxalEurope) Registry.
Kidney Int Rep
; 7(2): 210-220, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-35155860
18.
Prevalence of Hypertension in Children with Early-Stage ADPKD.
Clin J Am Soc Nephrol
; 13(6): 874-883, 2018 06 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29674338