"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
|
| MeSH Number(s) |
C12.777.419.630.477 C13.351.968.419.630.477
|
| 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
|
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 |
|---|
| 1996 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nephrosis, Lipoid" by people in Profiles.
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"Idiopathic" minimal change nephrotic syndrome: a podocyte mystery nears the end. Am J Physiol Renal Physiol. 2023 12 01; 325(6):F685-F694.
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Management of Adult Minimal Change Disease. Clin J Am Soc Nephrol. 2019 06 07; 14(6):911-913.
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Kidney-derived c-kit+ progenitor/stem cells contribute to podocyte recovery in a model of acute proteinuria. Sci Rep. 2018 10 03; 8(1):14723.
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Case series: CTLA4-IgG1 therapy in minimal change disease and focal segmental glomerulosclerosis. Pediatr Nephrol. 2015 Mar; 30(3):469-77.
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CD80 and suPAR in patients with minimal change disease and focal segmental glomerulosclerosis: diagnostic and pathogenic significance: response. Pediatr Nephrol. 2014 Aug; 29(8):1467-8.
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CD80 and suPAR in patients with minimal change disease and focal segmental glomerulosclerosis: diagnostic and pathogenic significance. Pediatr Nephrol. 2014 Aug; 29(8):1363-71.
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New insights into human minimal change disease: lessons from animal models. Am J Kidney Dis. 2012 Feb; 59(2):284-92.
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Minimal change disease as a modifiable podocyte paracrine disorder. Nephrol Dial Transplant. 2011 Jun; 26(6):1776-7.
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Filtering new facts about kidney disease. Nat Med. 2011 Jan; 17(1):44-5.
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Maximal 'CD80-uria' with minimal change. Kidney Int. 2010 Aug; 78(3):236-8.