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Lipoid nephrosis

Known as: Nephroses, Lipoid, Idiopathic Minimal Change Nephrotic Syndrome, change glomerulonephritis minimal 
A kidney disease with no or minimal histological glomerular changes on light microscopy and with no immune deposits. It is characterized by lipid… 
National Institutes of Health

Related topics

Related topics

13 relations
GlomerulonephritisIdiopathic Nephrotic SyndromeIn BloodKidney

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Model building for flavor changing Higgs couplings
If $t\rightarrow hq$ ($q=c,u$) or $h\rightarrow\tau\ell$ ($\ell=\mu,e$) decays are observed, it will be a clear signal of new… 
Review
2011
Review
2011
[Kidney involvement in rheumatoid arthritis].
Rheumatoid Arthritis (RA) is a widespread disease and its renal involvement, relatively common, is clinically significant because… 
Review
2010
Review
2010
Renal diseases with organized deposits: an algorithmic approach to classification and clinicopathologic diagnosis.
CONTEXT Most renal diseases with organized deposits are relatively uncommon conditions, and proper pathologic characterization… 
Highly Cited
2006
Highly Cited
2006
Acquiring Ontological Relationships from Wikipedia Using RMRS
We investigate the extraction of ontologies from biological text using a semantic representation derived from a robust parser… 
Highly Cited
2005
Highly Cited
2005
Discovery of biomarkers in human urine and cerebrospinal fluid by capillary electrophoresis coupled to mass spectrometry: Towards new diagnostic and therapeutic approaches
We report on our results using capillary electrophoresis coupled to mass spectrometry (CE‐MS) to examine human bodyfluids. To… 
Highly Cited
1988
Highly Cited
1988
Evidence suggesting a role for hydroxyl radical in puromycin aminonucleoside-induced proteinuria.
A single intravenous injection of puromycin aminonucleoside (PAN) results in marked proteinuria and glomerular morphological… 
Highly Cited
1983
Highly Cited
1983
N-acetyl-beta-glucosaminidase and beta 2-microglobulin. Their urinary excretion in patients with renal parenchymal disease.
The urinary excretion of N-acetyl-beta-glucosaminidase (NAG) and beta 2-microglobulin (beta 2M) was studied in 43 patients with… 
Highly Cited
1976
Highly Cited
1976
INHIBITION OF LYMPHOCYTE BLASTOGENESIS BY PLASMA OF PATIENTS WITH MINIMAL-CHANGE NEPHROTIC SYNDROME
Highly Cited
1968
Highly Cited
1968
Natural history of lipoid nephrosis and of membranous glomerulonephritis.
Abstract Twenty-one patient each with lipoid nephrosis (LN) and membranous glomerulonephritis (MGN) were observed for a long… 
Highly Cited
1935
Highly Cited
1935
Schüller-Christian Disease
THE case here described is the form of xanthomatosis (1), known as Schuller-Christian's disease, exhibiting “defects in the… 
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