Detalhe da pesquisa
1.
APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.
Nephrol Dial Transplant
; 34(11): 1885-1893, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29992269
2.
Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults.
Kidney Int
; 94(5): 1013-1022, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30348286
3.
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
Pediatr Nephrol
; 33(3): 473-483, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29058154
4.
INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.
N Engl J Med
; 365(25): 2377-88, 2011 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22187985
5.
LMX1B mutations cause hereditary FSGS without extrarenal involvement.
J Am Soc Nephrol
; 24(8): 1216-22, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23687361
6.
Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults.
Kidney Int
; 81(2): 179-89, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21900880
7.
Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.
J Am Soc Nephrol
; 22(2): 239-45, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21258034
8.
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
J Am Soc Nephrol
; 21(7): 1209-17, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20507940
9.
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
J Clin Invest
; 130(1): 335-344, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31613795
10.
Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.
J Am Soc Nephrol
; 19(10): 1871-8, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18614772
11.
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
J Clin Invest
; 132(11)2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35642643
12.
Long-term social outcome of children after kidney transplantation.
Transplantation
; 77(7): 1033-7, 2004 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15087767
13.
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
Kidney Int
; 66(2): 571-9, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15253708