"Nephrosis, Lipoid" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A kidney disease with no or minimal histological glomerular changes on light microscopy and with no immune deposits. It is characterized by lipid accumulation in the epithelial cells of KIDNEY TUBULES and in the URINE. Patients usually show NEPHROTIC SYNDROME indicating the presence of PROTEINURIA with accompanying EDEMA.
Descriptor ID |
D009402
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MeSH Number(s) |
C12.777.419.630.477 C13.351.968.419.630.477
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Concept/Terms |
Nephrosis, Lipoid- Nephrosis, Lipoid
- Lipoid Nephroses
- Lipoid Nephrosis
- Nephroses, Lipoid
- Minimal Change Glomerulopathy
- Minimal Change Disease
- Change Diseases, Minimal
- Disease, Minimal Change
- Diseases, Minimal Change
- Minimal Change Diseases
- Nephropathy, Minimal Change
- Minimal Change Nephropathies
- Minimal Change Nephropathy
- Nephropathies, Minimal Change
- Glomerulopathy, Minimal Change
- Glomerulopathies, Minimal Change
- Idiopathic Minimal Change Nephrotic Syndrome
Glomerulonephritis, Minimal Change- Glomerulonephritis, Minimal Change
- Glomerulonephritides, Minimal Change
- Minimal Change Glomerulonephritides
- Minimal Change Glomerulonephritis
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Below are MeSH descriptors whose meaning is more general than "Nephrosis, Lipoid".
Below are MeSH descriptors whose meaning is more specific than "Nephrosis, Lipoid".
This graph shows the total number of publications written about "Nephrosis, Lipoid" by people in this website by year, and whether "Nephrosis, Lipoid" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2007 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2018 | 2 | 0 | 2 |
2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Nephrosis, Lipoid" by people in Profiles.
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Diffuse membranoproliferative glomerulonephritis with focal sclerosis and renal amyloidosis in an adult male with autosomal dominant dystrophic epidermolysis bullosa: a case report. Ren Fail. 2019 Nov; 41(1):850-854.
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CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease. Am J Kidney Dis. 2019 02; 73(2):218-229.
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Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings. Pediatr Nephrol. 2018 10; 33(10):1773-1780.
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A reassessment of soluble urokinase-type plasminogen activator receptor in glomerular disease. Kidney Int. 2015 Mar; 87(3):564-74.
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Urinary cytokines and steroid responsiveness in idiopathic nephrotic syndrome of childhood. Am J Nephrol. 2008; 28(1):83-90.
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Cyclosporine therapy for steroid-resistant nephrotic syndrome. A controlled study. Am J Dis Child. 1988 Sep; 142(9):985-8.
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Urinary high density lipoprotein in minimal change glomerular disease and chronic glomerulopathies. Clin Chim Acta. 1979 May 16; 94(1):73-81.