Detalhe da pesquisa
1.
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.
Hum Genet
; 138(10): 1105-1115, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31230195
2.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
J Am Soc Nephrol
; 29(9): 2348-2361, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30143558
3.
Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children.
J Am Soc Nephrol
; 28(10): 3055-3065, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28566477
4.
The Child Health Care System of Serbia.
J Pediatr
; 177S: S156-S172, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27666265
5.
Associated extrarenal vascular diseases may complicate the treatment and outcome of renovascular hypertension.
Acta Paediatr
; 105(1): e35-41, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26437121
6.
Lack of IL7Rα expression in T cells is a hallmark of T-cell immunodeficiency in Schimke immuno-osseous dysplasia (SIOD).
Clin Immunol
; 161(2): 355-65, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26499378
7.
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.
Hum Genet
; 134(8): 905-16, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26026792
8.
Transcriptional and posttranscriptional mechanisms contribute to the dysregulation of elastogenesis in Schimke immuno-osseous dysplasia.
Pediatr Res
; 78(6): 609-17, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26309238
9.
Glomerular nestin expression: possible predictor of outcome of focal segmental glomerulosclerosis in children.
Pediatr Nephrol
; 30(1): 79-90, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25129203
10.
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
11.
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
12.
Genotype-phenotype associations in WT1 glomerulopathy.
Kidney Int
; 85(5): 1169-78, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24402088
13.
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
14.
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.
Hum Mutat
; 34(5): 714-24, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23418020
15.
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Kidney Int
; 84(1): 206-13, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23515051
16.
Pulmonary renal syndrome in a child with coexistence of anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane disease: case report and literature review.
BMC Nephrol
; 14: 66, 2013 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-23517575
17.
Granulomatosis with polyangiitis (Wegener's granulomatosis) in children: report of three cases with cutaneous manifestations and literature review.
Pediatr Dermatol
; 30(4): e37-42, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23145989
18.
Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.
Nat Genet
; 30(2): 215-20, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11799392
19.
Renal involvement in primary Sjogren syndrome of childhood: case report and literature review.
Mod Rheumatol
; 23(1): 182-9, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22484709
20.
Epidemiology of chronic kidney disease in children in Serbia.
Nephrol Dial Transplant
; 27(5): 1978-84, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22058136