"Kidney Diseases, Cystic" 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 heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC).
| Descriptor ID |
D052177
|
| MeSH Number(s) |
C12.777.419.403 C13.351.968.419.403
|
| Concept/Terms |
Kidney Diseases, Cystic- Kidney Diseases, Cystic
- Cystic Kidney Disease
- Disease, Cystic Kidney
- Diseases, Cystic Kidney
- Kidney Disease, Cystic
- Cystic Kidney Diseases
- Cystic Renal Diseases
- Cystic Renal Disease
- Disease, Cystic Renal
- Diseases, Cystic Renal
- Renal Disease, Cystic
- Renal Diseases, Cystic
Kidney, Cystic- Kidney, Cystic
- Cystic Kidney
- Cystic Kidneys
- Kidneys, Cystic
|
Below are MeSH descriptors whose meaning is more general than "Kidney Diseases, Cystic".
Below are MeSH descriptors whose meaning is more specific than "Kidney Diseases, Cystic".
This graph shows the total number of publications written about "Kidney Diseases, Cystic" by people in this website by year, and whether "Kidney Diseases, Cystic" 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 |
|---|
| 1994 | 1 | 0 | 1 |
| 1997 | 0 | 1 | 1 |
| 2001 | 1 | 1 | 2 |
| 2003 | 2 | 0 | 2 |
| 2005 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 1 | 2 |
| 2009 | 2 | 0 | 2 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 1 | 2 |
| 2013 | 0 | 2 | 2 |
| 2014 | 0 | 1 | 1 |
| 2015 | 4 | 2 | 6 |
| 2017 | 2 | 1 | 3 |
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 2 | 0 | 2 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Kidney Diseases, Cystic" by people in Profiles.
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Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation. AJNR Am J Neuroradiol. 2023 03; 44(3):334-340.
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Reply to "Comment: Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome". Neuropediatrics. 2022 08; 53(4):306-307.
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De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. Am J Med Genet A. 2022 08; 188(8):2360-2366.
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Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome. Neuropediatrics. 2022 06; 53(3):195-199.
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Teenager with a Unilateral Cloudy Eye. J Pediatr. 2021 06; 233:280.
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Nephronophthisis due to a novel DCDC2 variant in a patient from African-Caribbean descent: A case report. Am J Med Genet A. 2020 03; 182(3):527-531.
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Healthcare recommendations for Joubert syndrome. Am J Med Genet A. 2020 01; 182(1):229-249.
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Sclt1 deficiency causes cystic kidney by activating ERK and STAT3 signaling. Hum Mol Genet. 2017 08 01; 26(15):2949-2960.
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Characterization of Incidental Renal Mass With Dual-Energy CT: Diagnostic Accuracy of Effective Atomic Number Maps for Discriminating Nonenhancing Cysts From Enhancing Masses. AJR Am J Roentgenol. 2017 Oct; 209(4):W221-W230.
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Joubert syndrome: neuroimaging findings in 110 patients in correlation with cognitive function and genetic cause. J Med Genet. 2017 08; 54(8):521-529.