 Retinal Diseases
"Retinal Diseases" 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.
No definition found.
| Descriptor ID |
D012164
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| MeSH Number(s) |
C11.768
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| Concept/Terms |
Retinal Diseases- Retinal Diseases
- Disease, Retinal
- Diseases, Retinal
- Retinal Disease
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Below are MeSH descriptors whose meaning is more general than "Retinal Diseases".
Below are MeSH descriptors whose meaning is more specific than "Retinal Diseases".
This graph shows the total number of publications written about "Retinal Diseases" by people in this website by year, and whether "Retinal Diseases" 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 |
|---|
| 1982 | 2 | 1 | 3 | | 1998 | 1 | 0 | 1 | | 1999 | 1 | 0 | 1 | | 2001 | 0 | 1 | 1 | | 2003 | 1 | 0 | 1 | | 2005 | 1 | 1 | 2 | | 2006 | 1 | 0 | 1 | | 2008 | 4 | 1 | 5 | | 2009 | 3 | 0 | 3 | | 2010 | 1 | 0 | 1 | | 2011 | 2 | 0 | 2 | | 2014 | 2 | 0 | 2 | | 2015 | 3 | 0 | 3 | | 2016 | 2 | 0 | 2 | | 2017 | 1 | 0 | 1 | | 2018 | 2 | 0 | 2 | | 2019 | 2 | 0 | 2 |
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Below are the most recent publications written about "Retinal Diseases" by people in Profiles.
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McFarlane MT, Wright T, McCoy B, Snead OC, Westall CA. Retinal defect in children with infantile spasms of varying etiologies: An observational study. Neurology. 2020 02 11; 94(6):e575-e582.
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Shao Z, Tumber A, Maynes J, Tavares E, Kannu P, Heon E, Vincent A. Unique retinal signaling defect in GNB5-related disease. Doc Ophthalmol. 2020 06; 140(3):273-277.
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Liu H, Ji X, Dhaliwal S, Rahman SN, McFarlane M, Tumber A, Locke J, Wright T, Vincent A, Westall C. Evaluation of light- and dark-adapted ERGs using a mydriasis-free, portable system: clinical classifications and normative data. Doc Ophthalmol. 2018 12; 137(3):169-181.
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Rampasek L, Goldenberg A. Learning from Everyday Images Enables Expert-like Diagnosis of Retinal Diseases. Cell. 2018 02 22; 172(5):893-895.
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Wright T, Kumarappah A, Stavropoulos A, Reginald A, Buncic JR, Westall CA. VIGABATRIN TOXICITY IN INFANCY IS ASSOCIATED WITH RETINAL DEFECT IN ADOLESCENCE: A Prospective Observational Study. Retina. 2017 May; 37(5):858-866.
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Turner JM, Sauvé Y, Suh M, Wales PW, Wizzard P, Goruk S, Field CJ. A Third-Generation Lipid Emulsion that Contains n-3 Long-Chain PUFAs Preserves Retinal Function in Parenterally Fed Neonatal Piglets. J Nutr. 2016 Nov; 146(11):2260-2266.
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Takai H, Jenkinson E, Kabir S, Babul-Hirji R, Najm-Tehrani N, Chitayat DA, Crow YJ, de Lange T. A POT1 mutation implicates defective telomere end fill-in and telomere truncations in Coats plus. Genes Dev. 2016 04 01; 30(7):812-26.
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Merico D, Roifman M, Braunschweig U, Yuen RK, Alexandrova R, Bates A, Reid B, Nalpathamkalam T, Wang Z, Thiruvahindrapuram B, Gray P, Kakakios A, Peake J, Hogarth S, Manson D, Buncic R, Pereira SL, Herbrick JA, Blencowe BJ, Roifman CM, Scherer SW. Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing. Nat Commun. 2015 Nov 02; 6:8718.
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Westall CA, Wright T. Author Response. Neurology. 2015 Aug 18; 85(7):656.
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Lenassi E, Vincent A, Li Z, Saihan Z, Coffey AJ, Steele-Stallard HB, Moore AT, Steel KP, Luxon LM, Héon E, Bitner-Glindzicz M, Webster AR. A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants. Eur J Hum Genet. 2015 Oct; 23(10):1318-27.
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