 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 Harvard Catalyst Profiles by year, and whether "Ophthalmoplegia" was a major or minor topic of these publication.
Below are the most recent publications written about "Ophthalmoplegia" by people in Profiles.
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Tao WD, Liu M, Fisher M, Wang DR, Li J, Furie KL, Hao ZL, Lin S, Zhang CF, Zeng QT, Wu B. Posterior versus anterior circulation infarction: how different are the neurological deficits? Stroke. 2012 Aug; 43(8):2060-5.
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Desai J, Velo MP, Yamada K, Overman LM, Engle EC. Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). Gene Expr Patterns. 2012 May-Jun; 12(5-6):180-8.
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Kondo E, Nishimura T, Kosho T, Inaba Y, Mitsuhashi S, Ishida T, Baba A, Koike K, Nishino I, Nonaka I, Furukawa T, Saito K. Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing. Am J Med Genet A. 2012 Apr; 158A(4):772-8.
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Kurbanyan K, Lessell S. Intracranial hypotension and abducens palsy following upper spinal manipulation. Br J Ophthalmol. 2008 Jan; 92(1):153-5.
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Ferraris S, Clark S, Garelli E, Davidzon G, Moore SA, Kardon RH, Bienstock RJ, Longley MJ, Mancuso M, Gutiérrez Ríos P, Hirano M, Copeland WC, DiMauro S. Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1. Arch Neurol. 2008 Jan; 65(1):125-31.
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Heidary G, Engle EC, Hunter DG. Congenital fibrosis of the extraocular muscles. Semin Ophthalmol. 2008 Jan-Feb; 23(1):3-8.
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Bharucha DX, Campbell TB, Valencia I, Hardison HH, Kothare SV. MRI findings in pediatric ophthalmoplegic migraine: a case report and literature review. Pediatr Neurol. 2007 Jul; 37(1):59-63.
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Bosley TM, Oystreck DT, Robertson RL, al Awad A, Abu-Amero K, Engle EC. Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A. Brain. 2006 Sep; 129(Pt 9):2363-74.
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Yamada K, Hunter DG, Andrews C, Engle EC. A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon. Arch Ophthalmol. 2005 Sep; 123(9):1254-9.
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Quiñones-Hinojosa A, Lyon R, Du R, Lawton MT. Intraoperative motor mapping of the cerebral peduncle during resection of a midbrain cavernous malformation: technical case report. Neurosurgery. 2005 Apr; 56(2 Suppl):E439; discussion E439.
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