Permeability plasma factors in nephrotic syndrome: more than one factor, more than one inhibitor
Author:
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
http://academic.oup.com/ndt/article-pdf/16/5/882/23369744/160882.pdf
Reference18 articles.
1. Boute N, Gribouval O, Roselli S et al. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid‐resistant nephrotic syndrome. Nat Genet2000; 24: 349–354
2. Kaplan JM, Kim SH, North KN et al. Mutations in ACTN4, encoding alpha‐actinin‐4, cause familial focal segmental glomerulosclerosis. Nat Genet2000; 24: 251–256
3. Kestila M, Lenkkeri U, Mannikko M et al. Positionally cloned gene for a novel glomerular protein—nephrin—is mutated in congenital nephrotic syndrome. Mol Cell1998; 1: 575–582
4. Ingulli E, Tejani A. Incidence, treatment and outcome of recurrent focal segmental glomerulosclerosis posttransplantation in 42 allografts in children: a single‐center experience. Transplantation1991; 51: 401–405
5. Artero M, Biava C, Amend W, Tomlanovich S, Vincenti F. Recurrent focal glomerulosclerosis: natural history and response to therapy. Am J Med1992; 92: 3775
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