Detalhe da pesquisa
1.
A systematic approach to mapping recessive disease genes in individuals from outbred populations.
PLoS Genet
; 5(1): e1000353, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19165332
2.
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).
Nephrol Dial Transplant
; 23(4): 1291-7, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18065803
3.
NPHS3: new clues for understanding idiopathic nephrotic syndrome.
Pediatr Nephrol
; 23(6): 847-50, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18270750
4.
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
Pediatr Nephrol
; 23(9): 1455-60, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18543005
5.
Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
Pediatrics
; 119(4): e907-19, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17371932
6.
Childhood pineoblastoma: experiences from the prospective multicenter trials HIT-SKK87, HIT-SKK92 and HIT91.
J Neurooncol
; 81(2): 217-23, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16941074
7.
Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.
Pediatr Res
; 59(2): 325-31, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16439601