"Radiography" 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.
Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film).
Descriptor ID |
D011859
|
MeSH Number(s) |
E01.370.350.700
|
Concept/Terms |
Diagnostic X-Ray- Diagnostic X-Ray
- Diagnostic X Ray
- Diagnostic X-Rays
- X-Rays, Diagnostic
- Roentgenography
- X-Ray Radiology, Diagnostic
- X Ray Radiology, Diagnostic
- Radiology, Diagnostic X-Ray
- Radiology, Diagnostic X Ray
- X-Ray, Diagnostic
- X Ray, Diagnostic
- Diagnostic X-Ray Radiology
- Diagnostic X Ray Radiology
|
Below are MeSH descriptors whose meaning is more general than "Radiography".
Below are MeSH descriptors whose meaning is more specific than "Radiography".
This graph shows the total number of publications written about "Radiography" by people in this website by year, and whether "Radiography" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2001 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2008 | 0 | 1 | 1 |
2010 | 0 | 2 | 2 |
2012 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2015 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Radiography" by people in Profiles.
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Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2. Am J Med Genet A. 2017 Apr; 173(4):1102-1108.
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A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype. Am J Med Genet A. 2015 Mar; 167A(3):461-75.
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COL2A1 mutation as a cause of premature osteoarthritis in a 13-year-old child. Joint Bone Spine. 2014 Jan; 81(1):83-5.
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Mutation-based growth charts for SEDC and other COL2A1 related dysplasias. Am J Med Genet C Semin Med Genet. 2012 Aug 15; 160C(3):205-16.
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Small cell carcinoma of vulva: curative multimodal treatment in face of resistance to initial standard chemotherapy. Strahlenther Onkol. 2010 Sep; 186(9):521-4.
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Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1. Am J Med Genet A. 2010 May; 152A(5):1213-24.
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Down-regulation of CD28, TCR-zeta (zeta) and up-regulation of FAS in peripheral cytotoxic T-cells of primary breast cancer patients. Anticancer Res. 2008 Mar-Apr; 28(2A):779-84.
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Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother? Am J Med Genet A. 2007 Jun 01; 143A(11):1135-42.
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Evaluation of CA125, physical and radiological findings in follow-up of ovarian cancer patients. Anticancer Res. 2005 May-Jun; 25(3A):1551-4.
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Raine syndrome: report of a family with three affected sibs and further delineation of the syndrome. Clin Dysmorphol. 2003 Jul; 12(3):153-60.