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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
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Related topics
Related topics
12 relations
Autosomal recessive inheritance
Edema
Focal glomerulosclerosis
Hyperlipidemia
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Broader (1)
Nephrosis, congenital
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation
M. Malina
,
O. Cinek
,
J. Janda
,
T. Seeman
Pediatric nephrology (Berlin, West)
2009
Corpus ID: 80941
Autosomal recessive steroid-resistant nephrotic syndrome (NS) is a rare, genetically determined nephropathy caused mainly by a…
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Highly Cited
2004
Highly Cited
2004
Plasma Membrane Targeting of Podocin Through the Classical Exocytic Pathway: Effect of NPHS2 Mutations
S. Roselli
,
Imane Moutkine
,
O. Gribouval
,
Alexandre Benmerah
,
C. Antignac
Traffic : the International Journal of…
2004
Corpus ID: 26008262
Podocytes are specialized epithelial cells of the glomerulus in the kidney, which interconnect at the top of the glomerular…
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Highly Cited
2003
Highly Cited
2003
NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children
K. Maruyama
,
K. Iijima
,
+9 authors
N. Yoshikawa
Pediatric nephrology (Berlin, West)
2003
Corpus ID: 2093444
Abstract.Podocin is an integral membrane protein encoded by NPHS2, which is mapped to 1q25–31 and is exclusively expressed in…
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Highly Cited
2003
Highly Cited
2003
Intracellular mislocalization of mutant podocin and correction by chemical chaperones
Teiko Ohashi
,
K. Uchida
,
S. Uchida
,
S. Sasaki
,
H. Nihei
Histochemistry and Cell Biology
2003
Corpus ID: 24927819
The NPHS2 gene encoding the podocin protein was causally linked to the autosomal recessive type of steroid-resistant nephrotic…
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Review
2003
Review
2003
The Management of Idiopathic Nephrotic Syndrome in Children
E. Hodson
Paediatric drugs
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…
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Review
2002
Review
2002
Changing trends of histopathology in childhood nephrotic syndrome in western Saudi Arabia.
J. Kari
Saudi Medical Journal
2002
Corpus ID: 43274066
OBJECTIVE It is widely accepted that minimal change nephrotic syndrome is the most common cause of nephrosis in children. Recent…
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Review
1997
Review
1997
Cyclosporine in the therapy of steroid-resistant idiopathic nephrotic syndrome.
P. Niaudet
,
A. Fuchshuber
,
M. Gagnadoux
,
R. Habib
,
M. Broyer
Kidney international. Supplement
1997
Corpus ID: 30819252
Steroid-resistant nephrotic syndrome with either minimal changes or focal and segmental glomerular sclerosis on initial biopsy is…
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Highly Cited
1991
Highly Cited
1991
Treatment of idiopathic nephrotic syndrome with cyclosporin A in children.
P. Niaudet
,
M. Broyer
,
Renée Habib
Clinical Nephrology
1991
Corpus ID: 28056844
Cyclosporin A (CyA, Sandimmun) was given to 71 children with idiopathic nephrotic syndrome, 45 of whom were steroid-dependent…
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1984
1984
Treatment of Idiopathic Nephrotic Syndrome with Levamisole
P. Niaudet
,
R. Drachman
,
M. Gagnadoux
,
M. Broyer
Acta Paediatrica Scandinavica
1984
Corpus ID: 37741357
Thirty children with frequently relapsing idiopathic nephrotic syndrome (INS) were treated with levamisole (2.5 mg/kg BW) twice a…
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Highly Cited
1977
Highly Cited
1977
Decreased Serum Factor B Concentration Associated with Decreased Opsonization of Escherichia coli in the Idiopathic Nephrotic Syndrome
R. Mclean
,
A. Forsgren
,
B. Björkstén
,
Y. Kim
,
P. Quie
,
A. Michael
Pediatric Research
1977
Corpus ID: 9366832
Summary: We report correlative studies of factor B, properdin, C3, and the serum opsonic activity for Escherichia coli and…
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