Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Multifocal electroretinogram, mfERG"'
Publikováno v:
Ophthalmology and Therapy, Vol 12, Iss 5, Pp 2813-2816 (2023)
Externí odkaz:
https://doaj.org/article/e30f52df48a14e708c5898a383a6a3e2
Autor:
Sumit R Singh, Raja Narayanan
Publikováno v:
Indian Journal of Ophthalmology, Vol 67, Iss 10, Pp 1760-1762 (2019)
A 7-year-old boy presented with history of blunt trauma 1 month back. Best corrected visual acuity (BCVA) was 20/200 with optical coherence tomography (OCT) showing a large macular hole. Spontaneous closure of the macular hole seemed unlikely followi
Externí odkaz:
https://doaj.org/article/37aa32e7f310445881555e119c3b7c46
Publikováno v:
Indian Journal of Ophthalmology, Vol 65, Iss 9, Pp 877-879 (2017)
Alport syndrome is a rare hereditary disease that is associated with retinal abnormalities such as dot-and-fleck retinopathy and temporal macular thinning. The main pathophysiological process of Alport syndrome is loss of the collagen network in the
Externí odkaz:
https://doaj.org/article/68d69a3c8d204fa89301be7f1ea056f1
Autor:
Ait Ahmed Кh., Kamenskikh T.G.
Publikováno v:
Саратовский научно-медицинский журнал, Vol 10, Iss 2, Pp 308-313 (2014)
Purpose: to study the correlation between the results of the macular area responses by multifocal-electroretinog-raphy (mf-ERG) and the retina thickness obtained by the spectralis optical coherence tomography (ОСТ) in patients with age-related mac
Externí odkaz:
https://doaj.org/article/ddba3718be15438083f2550374bf0390
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 2
Journal of Clinical Medicine, Vol 10, Iss 357, p 357 (2021)
Volume 10
Issue 2
Journal of Clinical Medicine, Vol 10, Iss 357, p 357 (2021)
Background: The acute physiological changes induced by focal retinal photocoagulation (PC) have been largely unexplored. Methods: This was a case-series study. We recorded multifocal electroretinograms (mfERGs) just before PC, and mfERGs were also re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb79f0358b35adc9460508a2819d4de9
Publikováno v:
Middle East African Journal of Ophthalmology
We report two cases with foveal congenital simple hamartoma of the retinal pigment epithelium (CSHRPE), as both patients presented to our retina services complaining of a unilateral decreased vision. Full ophthalmic examination and multimodal imaging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51ebcd80f75bceb6a8050894807e6a41
https://pubmed.ncbi.nlm.nih.gov/32874047
https://pubmed.ncbi.nlm.nih.gov/32874047
Publikováno v:
Medicine
Hydroxychloroquine (HCQ), an analog of chloroquine, is widely used in various rheumatologic and dermatologic disorders. However, it may cause severe retinopathy with long-term use. The guidelines proposed by the American Academy of Ophthalmology sugg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb200d735d081638eaa95c948610987d
http://europepmc.org/articles/PMC6455786
http://europepmc.org/articles/PMC6455786
Publikováno v:
Indian Journal of Ophthalmology, Vol 65, Iss 9, Pp 877-879 (2017)
Indian Journal of Ophthalmology
Indian Journal of Ophthalmology
Alport syndrome is a rare hereditary disease that is associated with retinal abnormalities such as dot-and-fleck retinopathy and temporal macular thinning. The main pathophysiological process of Alport syndrome is loss of the collagen network in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d17b666e7eecba20ddcdf8c4555da32
http://www.ijo.in/article.asp?issn=0301-4738
http://www.ijo.in/article.asp?issn=0301-4738
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Akademický článek
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