Zobrazeno 1 - 9
of 9
pro vyhledávání: '"C B, Hoyng"'
Autor:
A M E Schauwvlieghe, G Dijkman, J M Hooymans, F D Verbraak, C B Hoyng, M G W Dijkgraaf, T Peto, J R Vingerling, R O Schlingemann
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0153052 (2016)
To compare the effectiveness of bevacizumab and ranibizumab in the treatment of exudative age-related macular degeneration (AMD).Multicentre, randomized, controlled, double-masked clinical trial in 327 patients. The non-inferiority margin was 4 lette
Externí odkaz:
https://doaj.org/article/e45a2c63efb948f29e52edb3987b2873
Publikováno v:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 105(11)
Fundus autofluorescence (FAF) may be excited and measured at different wavelengths. In the present study we compared short wavelength and near-infrared FAF patterns of retinal dystrophies.We analysed both eyes of 108 patients with diverse retinal dys
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 151(45)
A chart for measuring visual acuity is a better functional test than the routine distance visual acuity testing with single optotypes. The characteristics of a good reading chart are: logarithmically diminishing print size, simultaneous measurement o
Publikováno v:
Novartis Foundation symposium. 255
Mutations in the ABCA4 gene cause Stargardt disease (STGD), most cases with autosomal recessive (ar) cone-rod dystrophy (CRD), and some cases with atypical ar retinitis pigmentosa (arRP). We found compound heterozygous ABCA4 mutations in two unrelate
Publikováno v:
Eye (The Royal College of Ophthalmologists), 18, 939-40
Eye, 18(9), 939-940. Nature Publishing Group
Eye (The Royal College of Ophthalmologists), 18, 9, pp. 939-40
Eye, 18(9), 939-940. Nature Publishing Group
Eye (The Royal College of Ophthalmologists), 18, 9, pp. 939-40
Contains fulltext : 57255.pdf (Publisher’s version ) (Closed access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a7f3f55d63d021049086c98dedfdd21
http://hdl.handle.net/2066/57255
http://hdl.handle.net/2066/57255
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 146(34)
Autosomal recessive Stargardt disease is caused by mutations in the ABCA4 gene. Mutations in ABCA4 are also found in two-thirds of cases with autosomal recessive cone-rod dystrophy, and a small fraction of patients with autosomal recessive retinitis
Publikováno v:
Acta ophthalmologica Scandinavica. 80(4)
Experimental and epidemiological studies suggest that low antioxidant intake may be associated with the occurrence of neovascular age-related macular degeneration (AMD).We investigated this hypothesis further with a case-control study involving 72 ca
Autor:
J V, Ongkosuwito, E J, Feron, C E, van Doornik, A, Van der Lelij, C B, Hoyng, E C, La Heij, A, Kijlstra
Publikováno v:
Investigative ophthalmologyvisual science. 39(13)
To investigate the T-helper cell cytokine profiles in two well-defined clinical uveitis entities caused by an infectious mechanism.Cytokines (interleukin [IL]-2, IL-4, IL-6, IL-10, and interferon [IFN]-gamma) were measured in ocular fluid samples obt
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 142(4)
Age-related degeneration of the macula retinae occurs in two forms: the serious form with invasion of blood vessels and leakage, and the atrophic form. Both forms ultimately lead to a central scotoma. The prevalence of the terminal stage of age-relat