Detalhe da pesquisa
1.
Antibiotic Prophylaxis in Infants with Grade III, IV, or V Vesicoureteral Reflux.
N Engl J Med
; 389(11): 987-997, 2023 Sep 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37702442
2.
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
em Inglês
| MEDLINE | ID: mdl-38196016
3.
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.
J Med Genet
; 60(6): 587-596, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36379543
4.
A Rare De Novo Mutation in the TRIM8 Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report.
Int J Mol Sci
; 25(8)2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38674071
5.
Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression.
Pediatr Nephrol
; 38(5): 1499-1511, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36315273
6.
Assessment of Interleukin-15 (IL-15) Concentration in Children with Idiopathic Nephrotic Syndrome.
Int J Mol Sci
; 24(8)2023 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37108157
7.
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.
Am J Hum Genet
; 104(5): 994-1006, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31051115
8.
Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.
Nephrol Dial Transplant
; 37(12): 2474-2486, 2022 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35137195
9.
Diagnostic difficulties in the diagnosis of high acute-phase proteins levels in a teenage drug addicted female patient.
BMC Psychiatry
; 22(1): 509, 2022 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35902840
10.
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
J Am Soc Nephrol
; 32(4): 805-820, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33597122
11.
Assessment of Brain-Derived Neurotrophic Factor (BDNF) Concentration in Children with Idiopathic Nephrotic Syndrome.
Int J Mol Sci
; 23(20)2022 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36293164
12.
The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2).
Hum Mutat
; 42(4): 473-486, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33600043
13.
Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife.
Kidney Int
; 99(6): 1451-1458, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33309955
14.
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
15.
Mortality in Children Treated With Maintenance Peritoneal Dialysis: Findings From the International Pediatric Peritoneal Dialysis Network Registry.
Am J Kidney Dis
; 78(3): 380-390, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33549627
16.
Distal renal tubular acidosis: ERKNet/ESPN clinical practice points.
Nephrol Dial Transplant
; 36(9): 1585-1596, 2021 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33914889
17.
Ten-year trends in epidemiology and outcomes of pediatric kidney replacement therapy in Europe: data from the ESPN/ERA-EDTA Registry.
Pediatr Nephrol
; 36(8): 2337-2348, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33483800
18.
Atypical Hemolytic Uremic Syndrome (aHUS) and Adenosine Deaminase (ADA)-Deficient Severe Combined Immunodeficiency (SCID)-Two Diseases That Exacerbate Each Other: Case Report.
Int J Mol Sci
; 22(17)2021 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34502390
19.
Relationship between Gd-IgA1 and TNFR1 in IgA nephropathy and IgA vasculitis nephritis in children - multicenter study.
Cent Eur J Immunol
; 46(2): 199-209, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34764788
20.
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
N Engl J Med
; 376(8): 742-754, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28121514