 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
|
| MeSH Number(s) |
C11.270.684 C11.768.585.658.500 C16.320.290.684
|
| Concept/Terms |
Retinitis Pigmentosa- Retinitis Pigmentosa
- Cone-Rod Dystrophy
- Cone Rod Dystrophy
- Cone-Rod Dystrophies
- Dystrophies, Cone-Rod
- Dystrophy, Cone-Rod
- Tapetoretinal Degeneration
- Degeneration, Tapetoretinal
- Degenerations, Tapetoretinal
- Tapetoretinal Degenerations
- 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
|
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 this website 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 |
|---|
| 1991 | 1 | 0 | 1 | | 1992 | 1 | 0 | 1 | | 1994 | 1 | 0 | 1 | | 1995 | 2 | 0 | 2 | | 1996 | 1 | 0 | 1 | | 1997 | 2 | 0 | 2 | | 1998 | 4 | 0 | 4 | | 1999 | 1 | 0 | 1 | | 2001 | 1 | 0 | 1 | | 2002 | 1 | 0 | 1 | | 2003 | 2 | 0 | 2 | | 2004 | 1 | 0 | 1 | | 2005 | 4 | 0 | 4 | | 2006 | 1 | 0 | 1 | | 2007 | 2 | 0 | 2 | | 2009 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 | | 2019 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Retinitis Pigmentosa" by people in Profiles.
-
Okur V, Cho MT, van Wijk R, van Oirschot B, Picker J, Coury SA, Grange D, Manwaring L, Krantz I, Muraresku CC, Hulick PJ, May H, Pierce E, Place E, Bujakowska K, Telegrafi A, Douglas G, Monaghan KG, Begtrup A, Wilson A, Retterer K, Anyane-Yeboa K, Chung WK. De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment. Eur J Hum Genet. 2019 07; 27(7):1081-1089.
-
Walters EM, Wells KD, Bryda EC, Schommer S, Prather RS. Swine models, genomic tools and services to enhance our understanding of human health and diseases. Lab Anim (NY). 2017 Mar 22; 46(4):167-172.
-
Di Donato N, Neuhann T, Kahlert AK, Klink B, Hackmann K, Neuhann I, Novotna B, Schallner J, Krause C, Glass IA, Parnell SE, Benet-Pages A, Nissen AM, Berger W, Altmüller J, Thiele H, Weber BH, Schrock E, Dobyns WB, Bier A, Rump A. Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. J Med Genet. 2016 06; 53(6):419-25.
-
McAnany JJ, Alexander KR, Genead MA, Fishman GA. Equivalent intrinsic noise, sampling efficiency, and contrast sensitivity in patients with retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2013 Jun 03; 54(6):3857-62.
-
Ross JW, Fernandez de Castro JP, Zhao J, Samuel M, Walters E, Rios C, Bray-Ward P, Jones BW, Marc RE, Wang W, Zhou L, Noel JM, McCall MA, DeMarco PJ, Prather RS, Kaplan HJ. Generation of an inbred miniature pig model of retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2012 Jan 31; 53(1):501-7.
-
Paciorkowski AR, Shafrir Y, Hrivnak J, Patterson MC, Tennison MB, Clark HB, Gomez CM. Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms. Neurology. 2011 Sep 13; 77(11):1055-60.
-
Zhao C, Bellur DL, Lu S, Zhao F, Grassi MA, Bowne SJ, Sullivan LS, Daiger SP, Chen LJ, Pang CP, Zhao K, Staley JP, Larsson C. Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs. Am J Hum Genet. 2009 Nov; 85(5):617-27.
-
Kim LS, McAnany JJ, Alexander KR, Fishman GA. Intersession repeatability of humphrey perimetry measurements in patients with retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2007 Oct; 48(10):4720-4.
-
Apushkin MA, Fishman GA, Alexander KR, Shahidi M. Retinal thickness and visual thresholds measured in patients with retinitis pigmentosa. Retina. 2007 Mar; 27(3):349-57.
-
Alexander KR, Rajagopalan AS, Raghuram A, Fishman GA. Activation phase of cone phototransduction and the flicker electroretinogram in retinitis pigmentosa. Vision Res. 2006 Sep; 46(17):2773-85.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|