 Nephrotic Syndrome
"Nephrotic Syndrome" 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 condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction.
| Descriptor ID |
D009404
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| MeSH Number(s) |
C12.777.419.630.643 C13.351.968.419.630.643
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| Concept/Terms |
Nephrotic Syndrome- Nephrotic Syndrome
- Nephrotic Syndromes
- Syndrome, Nephrotic
- Syndromes, Nephrotic
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Below are MeSH descriptors whose meaning is more general than "Nephrotic Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Nephrotic Syndrome".
This graph shows the total number of publications written about "Nephrotic Syndrome" by people in this website by year, and whether "Nephrotic Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 | | 2003 | 1 | 0 | 1 | | 2004 | 2 | 0 | 2 | | 2005 | 1 | 0 | 1 | | 2007 | 1 | 2 | 3 | | 2009 | 1 | 0 | 1 | | 2011 | 1 | 1 | 2 | | 2013 | 3 | 0 | 3 | | 2017 | 1 | 1 | 2 | | 2018 | 3 | 2 | 5 | | 2019 | 1 | 0 | 1 | | 2021 | 2 | 0 | 2 | | 2022 | 2 | 0 | 2 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nephrotic Syndrome" by people in Profiles.
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Cara-Fuentes G, Verma R, Venkatareddy M, Bauer C, Piani F, Aksoy ST, Vazzalwar N, Garcia GE, Banks M, Ordo?ez FA, de Lucas-Collantes C, Bjornstad P, Gonz?lez Rodr?guez JD, Johnson RJ, Garg P. ?1-Integrin blockade prevents podocyte injury in experimental models of minimal change disease. Nefrologia (Engl Ed). 2024 Jan-Feb; 44(1):90-99.
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Campbell RE, Thurman JM. The Immune System and Idiopathic Nephrotic Syndrome. Clin J Am Soc Nephrol. 2022 12; 17(12):1823-1834.
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Cocorpus J, Jun J, Basalely A, Castellanos L, Singer P, Frank R, Bullaro O, Gurusinghe S, Sethna CB. Perceived family impact and coping mechanisms of caregivers of children with nephrotic syndrome. Pediatr Nephrol. 2023 Apr; 38(4):1177-1185.
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Trachtman H, Laskowski J, Lee C, Renner B, Feemster A, Parikh S, Panzer SE, Zhong W, Cravedi P, Cantarelli C, Kulik L, You Z, Satchell S, Rovin B, Liu F, Kalled SL, Holers VM, Jalal D, Thurman JM. Natural antibody and complement activation characterize patients with idiopathic nephrotic syndrome. Am J Physiol Renal Physiol. 2021 10 01; 321(4):F505-F516.
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Cara-Fuentes G, Smoyer WE. Biomarkers in pediatric glomerulonephritis and nephrotic syndrome. Pediatr Nephrol. 2021 09; 36(9):2659-2673.
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Majmundar AJ, Buerger F, Forbes TA, Kl?mbt V, Schneider R, Deutsch K, Kitzler TM, Howden SE, Scurr M, Tan KS, Krzeminski M, Widmeier E, Braun DA, Lai E, Ullah I, Amar A, Kolb A, Eddy K, Chen CH, Salmanullah D, Dai R, Nakayama M, Ottlewski I, Kolvenbach CM, Onuchic-Whitford AC, Mao Y, Mann N, Nabhan MM, Rosen S, Forman-Kay JD, Soliman NA, Heilos A, Kain R, Aufricht C, Mane S, Lifton RP, Shril S, Little MH, Hildebrandt F. Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice. Sci Adv. 2021 01; 7(1).
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Denburg MR, Razzaghi H, Bailey LC, Soranno DE, Pollack AH, Dharnidharka VR, Mitsnefes MM, Smoyer WE, Somers MJG, Zaritsky JJ, Flynn JT, Claes DJ, Dixon BP, Benton M, Mariani LH, Forrest CB, Furth SL. Using Electronic Health Record Data to Rapidly Identify Children with Glomerular Disease for Clinical Research. J Am Soc Nephrol. 2019 12; 30(12):2427-2435.
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Weaver J, Rove KO, Meenakshi-Sundaram B, Vricella GJ. Genetic Testing Proves Crucial in Case of Ambiguous Genitalia and Renal Masses. Urology. 2019 Jul; 129:194-196.
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Power BD, Walsh KP, Awan A, Waldron M, O'Grady MJ. Klippel-Feil syndrome as a novel feature of Schimke immunoosseous dysplasia. Am J Med Genet A. 2019 05; 179(5):862-863.
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Falko JM. Familial Chylomicronemia Syndrome: A Clinical Guide For Endocrinologists. Endocr Pract. 2018 08; 24(8):756-763.
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