Detalhe da pesquisa
1.
Control of blood pressure in hypertensive children and adolescents assessed by ambulatory blood pressure monitoring.
BMC Pediatr
; 24(1): 269, 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658852
2.
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload.
Hemoglobin
; 48(1): 47-55, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38369714
3.
Inadequate blood pressure control demonstrated by ambulatory blood pressure monitoring in pediatric renal transplant recipients.
Pediatr Transplant
; 23(6): e13499, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31157501
4.
Unusual cause of anemia in a child with end-stage renal disease: Questions.
Pediatr Nephrol
; 32(12): 2259-2260, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28255802
5.
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
J Am Soc Nephrol
; 25(9): 1917-22, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24700879
6.
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.
Kidney Int
; 85(6): 1429-33, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24429398
7.
Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.
Kidney Int
; 85(4): 880-7, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24257694
8.
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.
Kidney Int
; 85(6): 1310-7, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24152966
9.
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis.
Kidney Int
; 81(2): 196-200, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21900877
10.
Unusual cause of anemia in a child with end-stage renal disease: Answers.
Pediatr Nephrol
; 32(12): 2261-2262, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28255803
11.
Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.
J Am Soc Nephrol
; 22(10): 1815-20, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21903995
12.
Clinical Outcomes of Renal Replacement Therapy in Pediatric Acute Kidney Injury: A 10-Year Retrospective Observational Study.
Glob Pediatr Health
; 9: 2333794X221142415, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36544505
13.
Waist-to-height-ratio is associated with sustained hypertension in children and adolescents with high office blood pressure.
Front Cardiovasc Med
; 9: 1026606, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36712271
14.
Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24.
Nephrol Dial Transplant
; 25(5): 1496-501, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20007758
15.
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
Nephrol Dial Transplant
; 25(9): 2970-6, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20172850
16.
Outcomes of Empirical Antimicrobial Therapy for Pediatric Community-onset Febrile Urinary Tract Infection in the Era of Increasing Antimicrobial Resistance.
Pediatr Infect Dis J
; 39(2): 121-126, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31738320
17.
Henoch-Schönlein purpura from vasculitis to intestinal perforation: A case report and literature review.
World J Gastroenterol
; 22(26): 6089-94, 2016 Jul 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-27468201
18.
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.
Clin J Am Soc Nephrol
; 9(6): 1109-16, 2014 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24742477
19.
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.
J Clin Invest
; 123(8): 3243-53, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23867502
20.
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
J Clin Invest
; 121(5): 2013-24, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21540551