Afectación multigénica en el síndrome nefrótico congénito
Cobos-Carrascosa, Elena; Campos-Aguilera, Ana; Daza-Torres, Antonio.
Nefrología (Madr.)
; 34(2): 268-270, mar.-abr. 2014. tab
Artículo en Español | IBECS (España) | ID: ibc-124787
Documentos relacionados
Mendelian steroid resistant nephrotic syndrome in childhood: is it as common as reported?
New insights from the genetic work-up in early onset nephrotic syndrome: report from a registry in western India.
Genetic testing in steroid-resistant nephrotic syndrome: when and how?
Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome.
Familial forms of nephrotic syndrome.
Congenital nephrotic syndrome with a novel NPHS1 mutation.
Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome.
Congenital nephrotic syndrome with diffuse mesangial sclerosis caused by compound heterozygous mutation in LAMA5 gene.
Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.