Detalhe da pesquisa
1.
Risk factors for childhood chronic kidney disease: a population-based study.
Pediatr Nephrol
; 38(5): 1569-1576, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36018434
2.
Glomerular involvement in children with H syndrome.
Pediatr Nephrol
; 36(3): 721-724, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33387019
3.
[RENAL TUBULAR DYSGENESIS SECONDARY TO MUTATIONS IN GENES ENCODING THE RENIN-ANGIOTENSIN SYSTEM].
Harefuah
; 160(12): 822-826, 2021 Dec.
Artigo
em Hebraico
| MEDLINE | ID: mdl-34957720
4.
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I.
Ann Hum Genet
; 83(5): 361-366, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30977917
5.
Hodgkin's lymphoma, nephrotic syndrome, and echinococcosis cysts: an unusual association and literature review.
Pediatr Hematol Oncol
; 36(1): 40-45, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30784346
6.
Severe neutropenia in children after renal transplantation: incidence, course, and treatment with granulocyte colony-stimulating factor.
Pediatr Nephrol
; 30(11): 2029-36, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25994524
7.
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome.
Eur J Hum Genet
; 31(10): 1101-1107, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36599939
8.
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure.
Kidney Int Rep
; 8(10): 2126-2135, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37850020