Ophthalmoplegia
"Ophthalmoplegia" 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.
Paralysis of one or more of the ocular muscles due to disorders of the eye muscles, neuromuscular junction, supporting soft tissue, tendons, or innervation to the muscles.
Descriptor ID |
D009886
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MeSH Number(s) |
C10.292.562.750 C10.597.622.447 C11.590.472 C23.888.592.636.447
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Concept/Terms |
Ophthalmoplegia- Ophthalmoplegia
- Ophthalmoplegias
- Oculomotor Paralysis
- Paralysis, Oculomotor
Internal Ophthalmoplegia- Internal Ophthalmoplegia
- Internal Ophthalmoplegias
- Ophthalmoplegia, Internal
- Ophthalmoplegias, Internal
External Ophthalmoplegia- External Ophthalmoplegia
- External Ophthalmoplegias
- Ophthalmoplegia, External
- Ophthalmoplegias, External
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Below are MeSH descriptors whose meaning is more general than "Ophthalmoplegia".
Below are MeSH descriptors whose meaning is more specific than "Ophthalmoplegia".
This graph shows the total number of publications written about "Ophthalmoplegia" by people in UAMS Profiles by year, and whether "Ophthalmoplegia" 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 |
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2021 | 1 | 0 | 1 | 2019 | 1 | 0 | 1 | 2016 | 0 | 1 | 1 | 2007 | 2 | 0 | 2 | 2004 | 0 | 1 | 1 | 2003 | 1 | 0 | 1 | 2001 | 0 | 1 | 1 | 1999 | 1 | 0 | 1 | 1990 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ophthalmoplegia" by people in Profiles over the past ten years.
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O'Marro MB, Nazarian SM. Abduction Variant One-and-a-Half Syndrome Due to a Massive Right Hemispheric Stroke With Uncal Herniation and Rapid Intracranial Hypertension. J Neuroophthalmol. 2021 Sep 01; 41(3):e348-e350.
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Sommerville EW, Dalla Rosa I, Rosenberg MM, Bruni F, Thompson K, Rocha M, Blakely EL, He L, Falkous G, Schaefer AM, Yu-Wai-Man P, Chinnery PF, Hedstrom L, Spinazzola A, Taylor RW, Gorman GS. Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late-onset disorder of mitochondrial DNA maintenance. Clin Genet. 2020 02; 97(2):276-286.
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McKiernan P, Ball S, Santra S, Foster K, Fratter C, Poulton J, Craig K, McFarland R, Rahman S, Hargreaves I, Gupte G, Sharif K, Taylor RW. Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure. J Pediatr Gastroenterol Nutr. 2016 12; 63(6):592-597.
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