Detalhe da pesquisa
1.
Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment.
BMC Nephrol
; 20(1): 163, 2019 05 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31088395
2.
Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.
J Am Soc Nephrol
; 27(3): 722-9, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26139440
3.
Disparities in treatment and outcome of kidney replacement therapy in children with comorbidities: an ESPN/ERA Registry study.
Clin Kidney J
; 16(4): 745-755, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37007701
4.
Mycophenolate mofetil for steroid-dependent nephrotic syndrome: a phase II Bayesian trial.
Pediatr Nephrol
; 27(3): 389-96, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21947272
5.
Social Deprivation Is Associated With Lower Access to Pre-emptive Kidney Transplantation and More Urgent-Start Dialysis in the Pediatric Population.
Kidney Int Rep
; 7(4): 741-751, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35497781
6.
Renal Prognosis in Children With Tubulointerstitial Nephritis and Uveitis Syndrome.
Kidney Int Rep
; 6(12): 3045-3053, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34901573
7.
Population pharmacokinetics and Bayesian estimator of mycophenolic acid in children with idiopathic nephrotic syndrome.
Br J Clin Pharmacol
; 69(4): 358-66, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20406220
8.
Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trial.
BMJ Open
; 10(9): e037306, 2020 09 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32967877
9.
School level of children carrying a HNF1B variant or a deletion.
Eur J Hum Genet
; 28(1): 56-63, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31481685
10.
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Nephrol Dial Transplant
; 24(5): 1455-64, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19096086
11.
Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation.
Clin Chim Acta
; 481: 1-8, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29476731
12.
Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.
Clin J Am Soc Nephrol
; 13(2): 242-250, 2018 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29146702
13.
[Recommendations for management of patients from pediatrics unit to adult unit: Transition and transfer program]. / Transition et transfert de la néphrologie pédiatrique à la néphrologie adulte : recommandations de la filière maladies rénales rares ORKiD.
Nephrol Ther
; 17(2): 137-142, 2021 04.
Artigo
em Francês
| MEDLINE | ID: mdl-33531259
14.
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
J Clin Endocrinol Metab
; 101(5): 2185-95, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26963950
15.
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.
Nat Genet
; 44(4): 456-60, S1-3, 2012 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-22406640
16.
Darbepoetin, effective treatment of anaemia in paediatric patients with chronic renal failure.
Pediatr Nephrol
; 22(5): 708-14, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17216497
17.
Clinical quiz. Loin pain haematuria syndrome.
Pediatr Nephrol
; 17(3): 217-9, 2002 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11956864
18.
Estudo da atividade de um centro de hemodiálise infantil
J. bras. nefrol
; 10(3): 103-12, set. 1988.
Artigo
em Português
| LILACS | ID: lil-71331