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
em Inglês
| MEDLINE | ID: mdl-38196016
2.
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Hum Mol Genet
; 29(22): 3662-3678, 2020 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33276377
3.
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
4.
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
5.
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
6.
Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort.
Nephrol Dial Transplant
; 33(1): 85-94, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27708066
7.
The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.
J Am Soc Nephrol
; 28(10): 3066-3075, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28526779
8.
[B-type natriuretic peptide as a marker of cardiac dysfunction in children with chronic kidney disease]. / Peptyd natriuretyczny typu B jako marker uszkodzenia serca u dzieci z przewlekla choroba nerek.
Pol Merkur Lekarski
; 44(262): 171-176, 2018 Apr 23.
Artigo
em Polonês
| MEDLINE | ID: mdl-29775443
9.
Filter Size Not the Anticoagulation Method is the Decisive Factor in Continuous Renal Replacement Therapy Circuit Survival.
Kidney Blood Press Res
; 42(2): 327-337, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28578343
10.
What has changed in the prevalence of hypertension in dialyzed children during the last decade?
Ren Fail
; 39(1): 283-289, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27882810
11.
Chronic Kidney Disease-associated Pruritus in Children.
Acta Derm Venereol
; 96(7): 938-942, 2016 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27171238
12.
Modification of the Schwartz equations for children increases their accuracy at eGFR > 60 mL/min/1.73 m(2).
Ren Fail
; 38(5): 787-98, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27056090
13.
Hemolytic uremic syndrome with Mycoplasma pneumoniae infection and membrane cofactor protein mutation case report.
Przegl Lek
; 73(11): 862-4, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-29693967
14.
Favorable four-yr outcome after renal transplantation in a patient with complement factor H antibody and CFHR1/CFHR3 gene mutation-associated HUS.
Pediatr Transplant
; 19(6): E130-4, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26087050
15.
Disturbed skin barrier in children with chronic kidney disease.
Pediatr Nephrol
; 30(2): 333-8, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25127919
16.
Relationship between serum IgA/C3 ratio and severity of histological lesions using the Oxford classification in children with IgA nephropathy.
Pediatr Nephrol
; 30(7): 1113-20, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25549975
17.
[Do we successfully treat anemia and calcium-phosphate disorders in children with chronic kidney disease at the beginning of the twenty-first century?]. / Czy na poczatku XXI wieku skutecznie leczymy niedokrwistosc i zaburzenia wapniowo-fosforanowe u dzieci z przewlekla choroba nerek?
Przegl Lek
; 72(7): 349-53, 2015.
Artigo
em Polonês
| MEDLINE | ID: mdl-26817347
18.
Clinical validity of urinary interleukin 18 and interleukin 6 determinations in preterm newborns.
Przegl Lek
; 72(11): 589-96, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27012114
19.
Acute kidney injury in a single pediatric intensive care unit in Poland: a retrospective study.
Kidney Blood Press Res
; 39(1): 28-39, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24854084
20.
[Familial case of oral-facial-digital syndrome type 1 (OFD 1)]. / Rodzinny przypadek zespolu ustno-twarzowo-palcowego typu 1 (OFD 1).
Przegl Lek
; 71(2): 110-4, 2014.
Artigo
em Polonês
| MEDLINE | ID: mdl-25016787