 Retinitis Pigmentosa
"Retinitis Pigmentosa" 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.
Hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field.
| Descriptor ID |
D012174
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| MeSH Number(s) |
C11.270.684 C11.768.585.658.500 C16.320.290.684
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| Concept/Terms |
Retinitis Pigmentosa- Retinitis Pigmentosa
- Cone-Rod Dystrophy
- Cone Rod Dystrophy
- Cone-Rod Dystrophies
- Dystrophies, Cone-Rod
- Dystrophy, Cone-Rod
- Cone-Rod Retinal Dystrophy
- Cone Rod Retinal Dystrophy
- Cone-Rod Retinal Dystrophies
- Dystrophies, Cone-Rod Retinal
- Dystrophy, Cone-Rod Retinal
- Retinal Dystrophies, Cone-Rod
- Retinal Dystrophy, Cone-Rod
- Tapetoretinal Degeneration
- Degeneration, Tapetoretinal
- Degenerations, Tapetoretinal
- Tapetoretinal Degenerations
- Retinal Cone-Rod Dystrophy
- Cone-Rod Dystrophies, Retinal
- Cone-Rod Dystrophy, Retinal
- Dystrophies, Retinal Cone-Rod
- Dystrophy, Retinal Cone-Rod
- Retinal Cone Rod Dystrophy
- Retinal Cone-Rod Dystrophies
- Rod Cone Dystrophies
- Dystrophies, Rod Cone
- Dystrophy, Rod Cone
- Rod Cone Dystrophy
- Rod-Cone Dystrophy
- Dystrophies, Rod-Cone
- Dystrophy, Rod-Cone
- Rod-Cone Dystrophies
- Cone-Rod Degenerations
- Cone Rod Degenerations
- Cone-Rod Degeneration
- Degeneration, Cone-Rod
- Degenerations, Cone-Rod
- Pigmentary Retinopathy
- Pigmentary Retinopathies
- Retinopathies, Pigmentary
- Retinopathy, Pigmentary
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Below are MeSH descriptors whose meaning is more general than "Retinitis Pigmentosa".
Below are MeSH descriptors whose meaning is more specific than "Retinitis Pigmentosa".
This graph shows the total number of publications written about "Retinitis Pigmentosa" by people in UAMS Profiles by year, and whether "Retinitis Pigmentosa" 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 |
|---|
| 2024 | 1 | 0 | 1 | | 2023 | 2 | 0 | 2 | | 2020 | 0 | 1 | 1 | | 2017 | 0 | 1 | 1 | | 2002 | 1 | 0 | 1 | | 1996 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Retinitis Pigmentosa" by people in Profiles over the past ten years.
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Georgiou M, Shakarchi AF, Elhusseiny AM, Michaelides M, Sallam AB. Cataract Surgery Outcomes in Retinitis Pigmentosa A Comparative Clinical Database Study. Am J Ophthalmol. 2024 06; 262:34-39.
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Musleh AM, AlRyalat SA, Abid MN, Salem Y, Hamila HM, Sallam AB. Diagnostic accuracy of artificial intelligence in detecting retinitis pigmentosa: A systematic review and meta-analysis. Surv Ophthalmol. 2024 May-Jun; 69(3):411-417.
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Georgiou M, Robson AG, Uwaydat SH, Ji MH, Shakarchi AF, Pontikos N, Mahroo OA, Cheetham ME, Webster AR, Hardcastle AJ, Michaelides M. RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers. Am J Ophthalmol. 2024 05; 261:112-120.
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Ahuja P, Sharifi A, Pakravan M, Schefler AC, Lee AG. Hydroxychloroquine toxicity unmasking an occult retinitis pigmentosa carrier. Can J Ophthalmol. 2023 08; 58(4):e179-e181.
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Huckfeldt RM, Grigorian F, Place E, Comander JI, Vavvas D, Young LH, Yang P, Shurygina M, Pierce EA, Pennesi ME. Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum. Mol Vis. 2020; 26:423-433.
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Khurana S, Saini V, Wadhwa V, Kaur H. Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation. J Ultrasound. 2017 Jun; 20(2):167-170.
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