"Calcinosis" 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.
Pathologic deposition of calcium salts in tissues.
Descriptor ID |
D002114
|
MeSH Number(s) |
C18.452.174.130
|
Concept/Terms |
Calcinosis- Calcinosis
- Calcinoses
- Calcification, Pathologic
- Pathologic Calcification
|
Below are MeSH descriptors whose meaning is more general than "Calcinosis".
Below are MeSH descriptors whose meaning is more specific than "Calcinosis".
This graph shows the total number of publications written about "Calcinosis" by people in this website by year, and whether "Calcinosis" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
---|
1995 | 1 | 0 | 1 |
2006 | 0 | 1 | 1 |
2011 | 0 | 1 | 1 |
2013 | 2 | 0 | 2 |
2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "Calcinosis" by people in Profiles.
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A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome. Am J Hum Genet. 2015 Feb 05; 96(2):275-82.
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Mitral and aortic valve sclerosis/calcification and carotid atherosclerosis: results from 1065 patients. Heart Vessels. 2014 Nov; 29(6):776-83.
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Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. BMC Med Genet. 2013 Feb 08; 14:23.
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RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies. PLoS One. 2011; 6(12):e25734.
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Prenatal ultrasound diagnosis, follow-up, and outcome of congenital varicella syndrome. Fetal Diagn Ther. 2006; 21(3):296-301.
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A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome? Genet Couns. 1995; 6(4):297-302.