Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome
- 1 August 2004
- journal article
- Published by Elsevier BV in Kidney International
- Vol. 66 (2), 564-570
- https://doi.org/10.1111/j.1523-1755.2004.00775.x
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic SyndromeJournal of the American Society of Nephrology, 2004
- Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathyJournal of Medical Genetics, 2000
- Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?Clinical Endocrinology, 2000
- Evidence for the Genetic Heterogeneity of Nephropathic Phenotypes Associated with Denys-Drash and Frasier SyndromesAmerican Journal of Human Genetics, 1999
- Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation DatabaseAmerican Journal of Human Genetics, 1998
- Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic SyndromeMolecular Cell, 1998
- SHORT VERSUS STANDARD PREDNISONE THERAPY FOR INITIAL TREATMENT OF IDIOPATHIC NEPHROTIC SYNDROME IN CHILDRENThe Lancet, 1988
- Primary nephrotic syndrome in children: Clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularityKidney International, 1981
- A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal diseaseThe Journal of Pediatrics, 1970
- Gonadoblastoma associated with pure gonadal dysgenesis in monozygous twinsThe Journal of Pediatrics, 1964