 Calcinosis
"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
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| MeSH Number(s) |
C18.452.174.130
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| Concept/Terms |
Calcinosis- Calcinosis
- Calcinoses
- Pathologic Calcification
- Calcification, Pathologic
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1983 | 1 | 2 | 3 | | 1985 | 1 | 0 | 1 | | 1986 | 1 | 1 | 2 | | 1989 | 0 | 1 | 1 | | 1991 | 0 | 1 | 1 | | 1994 | 1 | 0 | 1 | | 1995 | 0 | 2 | 2 | | 1997 | 1 | 0 | 1 | | 1998 | 1 | 1 | 2 | | 1999 | 0 | 1 | 1 | | 2000 | 0 | 1 | 1 | | 2002 | 0 | 1 | 1 | | 2003 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2006 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2008 | 0 | 1 | 1 | | 2009 | 1 | 1 | 2 | | 2014 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2016 | 2 | 0 | 2 | | 2018 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Calcinosis" by people in Profiles.
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Dushnicky MJ, Okura H, Shroff M, Laxer RM, Kulkarni AV. Pediatric Idiopathic Intervertebral Disc Calcification: Single-Center Series and Review of the Literature. J Pediatr. 2019 03; 206:212-216.
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Gsell KY, Zwambag DP, Fournier DE, Séguin CA, Brown SHM. Paraspinal Muscle Passive Stiffness Remodels in Direct Response to Spine Stiffness: A Study Using the ENT1-Deficient Mouse. Spine (Phila Pa 1976). 2017 Oct 01; 42(19):1440-1446.
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Mehta K, Dell S, Birken C, Al-Saleh S. Pulmonary Alveolar Microlithiasis. Can Respir J. 2016; 2016:4938632.
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Takai H, Jenkinson E, Kabir S, Babul-Hirji R, Najm-Tehrani N, Chitayat DA, Crow YJ, de Lange T. A POT1 mutation implicates defective telomere end fill-in and telomere truncations in Coats plus. Genes Dev. 2016 04 01; 30(7):812-26.
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Rutsch F, MacDougall M, Lu C, Buers I, Mamaeva O, Nitschke Y, Rice GI, Erlandsen H, Kehl HG, Thiele H, Nürnberg P, Höhne W, Crow YJ, Feigenbaum A, Hennekam RC. 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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Reich A, Bae AS, Barnes AM, Cabral WA, Hinek A, Stimec J, Hill SC, Chitayat D, Marini JC. Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expression. J Clin Endocrinol Metab. 2015 Feb; 100(2):E325-32.
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Rider LG, Lachenbruch PA, Monroe JB, Ravelli A, Cabalar I, Feldman BM, Villalba ML, Myones BL, Pachman LM, Rennebohm RM, Reed AM, Miller FW. Damage extent and predictors in adult and juvenile dermatomyositis and polymyositis as determined with the myositis damage index. Arthritis Rheum. 2009 Nov; 60(11):3425-35.
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Dimaras H, Khetan V, Halliday W, Héon E, Chan HS, Gallie BL. Retinoma underlying retinoblastoma revealed after tumor response to 1 cycle of chemotherapy. Arch Ophthalmol. 2009 Aug; 127(8):1066-8.
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Rodés-Cabau J, Houde C, Perron J, Benson LN, Pibarot P. Delayed improvement in valve hemodynamic performance after percutaneous pulmonary valve implantation. Ann Thorac Surg. 2008 May; 85(5):1787-8.
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Kannu P, McFarlane JH, Savarirayan R, Aftimos S. An unclassifiable short rib-polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblings. . 2007 Nov 01; 143A(21):2607-11.
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