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Idiopathic Nephrotic Syndrome

Known as: NEPHROTIC SYNDROME, TYPE 2, NPHS2, Nephrotic Syndrome, Idiopathic 
Nephrotic syndrome for which no cause has been identified.(NICHD)
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Autosomal recessive steroid-resistant nephrotic syndrome (NS) is a rare, genetically determined nephropathy caused mainly by a… 
Highly Cited
2004
Highly Cited
2004
Podocytes are specialized epithelial cells of the glomerulus in the kidney, which interconnect at the top of the glomerular… 
Highly Cited
2003
Highly Cited
2003
Abstract.Podocin is an integral membrane protein encoded by NPHS2, which is mapped to 1q25–31 and is exclusively expressed in… 
Highly Cited
2003
Highly Cited
2003
The NPHS2 gene encoding the podocin protein was causally linked to the autosomal recessive type of steroid-resistant nephrotic… 
Review
2003
Review
2003
  • E. Hodson
  • 2003
  • Corpus ID: 34180683
Childhood nephrotic syndrome is a rare condition with an incidence of 1–2 per 100 000 children aged below 16 years. Untreated… 
Review
2002
Review
2002
OBJECTIVE It is widely accepted that minimal change nephrotic syndrome is the most common cause of nephrosis in children. Recent… 
Review
1997
Review
1997
Steroid-resistant nephrotic syndrome with either minimal changes or focal and segmental glomerular sclerosis on initial biopsy is… 
Highly Cited
1991
Highly Cited
1991
Cyclosporin A (CyA, Sandimmun) was given to 71 children with idiopathic nephrotic syndrome, 45 of whom were steroid-dependent… 
1984
1984
Thirty children with frequently relapsing idiopathic nephrotic syndrome (INS) were treated with levamisole (2.5 mg/kg BW) twice a… 
Highly Cited
1977
Highly Cited
1977
Summary: We report correlative studies of factor B, properdin, C3, and the serum opsonic activity for Escherichia coli and…