Found: 12
Select item for more details and to access through your institution.
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).
- Published in:
- Nephrology Dialysis Transplantation, 2008, v. 23, n. 4, p. 1291
- By:
- Publication type:
- Article
Focal segmental glomerulosclerosis is not a sufficient predictor of renal outcome in patients with membranous nephropathy.
- Published in:
- Nephrology Dialysis Transplantation, 2007, v. 22, n. 8, p. 2201, doi. 10.1093/ndt/gfm188
- By:
- Publication type:
- Article
Utility of Urinary Biomarkers in Fabry Disease.
- Published in:
- Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 4, p. 108
- By:
- Publication type:
- Article
A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 1, p. 1, doi. 10.1371/journal.pgen.1000353
- By:
- Publication type:
- Article
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
- Published in:
- Nephrology Dialysis Transplantation, 2010, v. 25, n. 9, p. 2970, doi. 10.1093/ndt/gfq088
- By:
- Publication type:
- Article
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
- Published in:
- Nephrology Dialysis Transplantation, 2008, v. 23, n. 11, p. 3527, doi. 10.1093/ndt/gfn271
- By:
- Publication type:
- Article
Membranoproliferative glomerulonephritis associated with a mutation in Wilms’ tumour suppressor gene 1.
- Published in:
- 2009
- By:
- Publication type:
- Report
Complete remission of nephrotic syndrome in an infant with focal segmental glomerulosclerosis: is it renin–angiotensin blockade?
- Published in:
- 2009
- By:
- Publication type:
- Report
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2008, v. 23, n. 9, p. 1455, doi. 10.1007/s00467-008-0861-7
- By:
- Publication type:
- Article
Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life.
- Published in:
- Kidney International, 2009, v. 75, n. 7, p. 669, doi. 10.1038/ki.2008.693
- By:
- Publication type:
- Article
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Kidney Diseases Caused by Complement Dysregulation: Acquired, Inherited, and Still More to Come.
- Published in:
- Clinical & Developmental Immunology, 2012, p. 1, doi. 10.1155/2012/695131
- By:
- Publication type:
- Article