 Electroretinography
"Electroretinography" 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.
Recording of electric potentials in the retina after stimulation by light.
| Descriptor ID |
D004596
|
| MeSH Number(s) |
E01.370.380.225 E01.370.405.270
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Electroretinography".
Below are MeSH descriptors whose meaning is more specific than "Electroretinography".
This graph shows the total number of publications written about "Electroretinography" by people in this website by year, and whether "Electroretinography" 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 |
|---|
| 1993 | 1 | 0 | 1 | | 1994 | 0 | 1 | 1 | | 1998 | 1 | 0 | 1 | | 2000 | 0 | 1 | 1 | | 2001 | 1 | 0 | 1 | | 2002 | 0 | 3 | 3 | | 2003 | 3 | 1 | 4 | | 2004 | 0 | 2 | 2 | | 2005 | 0 | 1 | 1 | | 2006 | 1 | 1 | 2 | | 2007 | 1 | 2 | 3 | | 2008 | 1 | 4 | 5 | | 2010 | 1 | 1 | 2 | | 2011 | 0 | 5 | 5 | | 2012 | 2 | 3 | 5 | | 2013 | 1 | 4 | 5 | | 2014 | 2 | 1 | 3 | | 2015 | 0 | 1 | 1 | | 2016 | 0 | 1 | 1 | | 2017 | 0 | 5 | 5 | | 2018 | 2 | 2 | 4 | | 2019 | 1 | 3 | 4 | | 2020 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Electroretinography" by people in Profiles.
-
Duncan JL, Liang W, Maguire MG, Audo I, Ayala AR, Birch DG, Carroll J, Cheetham JK, Esposti SD, Durham TA, Erker L, Farsiu S, Ferris FL, Heon E, Hufnagel RB, Iannaccone A, Jaffe GJ, Kay CN, Michaelides M, Pennesi ME, Sahel JA. Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity. Am J Ophthalmol. 2020 11; 219:87-100.
-
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.
-
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.
-
Mastey RR, Georgiou M, Langlo CS, Kalitzeos A, Patterson EJ, Kane T, Singh N, Vincent A, Moore AT, Tsang SH, Lin JH, Young MP, Hartnett ME, Héon E, Kohl S, Michaelides M, Carroll J. Characterization of Retinal Structure in ATF6-Associated Achromatopsia. Invest Ophthalmol Vis Sci. 2019 06 03; 60(7):2631-2640.
-
Ji X, McFarlane M, Liu H, Dupuis A, Westall CA. Hand-held, dilation-free, electroretinography in children under 3 years of age treated with vigabatrin. Doc Ophthalmol. 2019 06; 138(3):195-203.
-
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.
-
Cideciyan AV, Charng J, Roman AJ, Sheplock R, Garafalo AV, Heon E, Jacobson SG. Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 Years. Invest Ophthalmol Vis Sci. 2018 09 04; 59(11):4558-4566.
-
Vincent A, Macrì A, Tumber A, Koukas N, Ahonen S, Striano P, Minassian B. Ocular phenotype and electroretinogram abnormalities in Lafora disease: A "window to the brain". Neurology. 2018 07 17; 91(3):137-139.
-
Hirji N, Bradley PD, Li S, Vincent A, Pennesi ME, Thomas AS, Heon E, Bhan A, Mahroo OA, Robson A, Inglehearn CF, Moore AT, Michaelides M. Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta. Am J Ophthalmol. 2018 04; 188:123-130.
-
Gerth-Kahlert C, Tiwari A, Hanson JVM, Batmanabane V, Traboulsi E, Pennesi ME, Al-Qahtani AA, Lam BL, Heckenlively J, Zweifel SA, Vincent A, Fierz F, Barthelmes D, Branham K, Khan N, Bahr A, Baehr L, Magyar I, Koller S, Azzarello-Burri S, Niedrist D, Heon E, Berger W. C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. Invest Ophthalmol Vis Sci. 2017 08 01; 58(10):3840-3850.
|
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.
|