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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1997 2
2003 1
2004 1
2006 1
2008 2
2009 1
2010 2
2012 1
2013 2
2014 1
2015 1
2016 2
2018 1
2019 3
2020 2
2021 3
2022 1
2023 3
2024 2

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28 results

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Page 1
A review of neovascular glaucoma. Etiopathogenesis and treatment.
Dumbrăveanu L, Cușnir V, Bobescu D. Dumbrăveanu L, et al. Rom J Ophthalmol. 2021 Oct-Dec;65(4):315-329. doi: 10.22336/rjo.2021.66. Rom J Ophthalmol. 2021. PMID: 35087972 Free PMC article. Review.
The most common causes of NVG are: central retinal vein occlusion, proliferative diabetic retinopathy, and ocular ischemic syndrome. Once the gonioscopy developed as a part of clinical examination, it became possible to visualize the new vessels of the anterior segment of …
The most common causes of NVG are: central retinal vein occlusion, proliferative diabetic retinopathy, and ocular ischemic syndrome. Once th …
Ophthalmic genetics/inherited eye disease.
Young TL. Young TL. Curr Opin Ophthalmol. 2003 Oct;14(5):296-303. doi: 10.1097/00055735-200310000-00011. Curr Opin Ophthalmol. 2003. PMID: 14502058 Review.
RECENT FINDINGS: Most genetic ocular disorders are not yet treatable and/or are without curative therapies because of our limited understanding of pathogenesis, and the need for well-designed and fully implemented animal model or human clinical trial testing of ther …
RECENT FINDINGS: Most genetic ocular disorders are not yet treatable and/or are without curative therapies because of our limited understand …
INTRAVITREAL RANIBIZUMAB TREATMENT FOR ADVANCED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH HIGH VASCULAR ACTIVITY.
Lyu J, Zhang Q, Xu Y, Zhang X, Fei P, Zhao P. Lyu J, et al. Retina. 2021 Sep 1;41(9):1976-1985. doi: 10.1097/IAE.0000000000003122. Retina. 2021. PMID: 34432746 Free PMC article.
Familial exudative vitreoretinopathy-causative genetic mutations in 11 patients were related to variable response to IVR treatment. ...Different treatment outcomes may be relevant to variable presentation and genetic heterogeneity of familial exudat
Familial exudative vitreoretinopathy-causative genetic mutations in 11 patients were related to variable response to IV
Retinoblastoma frontiers with intravenous, intra-arterial, periocular, and intravitreal chemotherapy.
Shields CL, Fulco EM, Arias JD, Alarcon C, Pellegrini M, Rishi P, Kaliki S, Bianciotto CG, Shields JA. Shields CL, et al. Eye (Lond). 2013 Feb;27(2):253-64. doi: 10.1038/eye.2012.175. Epub 2012 Sep 21. Eye (Lond). 2013. PMID: 22995941 Free PMC article. Review.
Children 2 years old showed leading pseudoretinoblastomas of persistent fetal vasculature, Coats disease, and vitreous haemorrhage, whereas those >5 years showed simulators of Coats, toxocariasis, and familial exudative vitreoretinopathy. The diagnosis of …
Children 2 years old showed leading pseudoretinoblastomas of persistent fetal vasculature, Coats disease, and vitreous haemorrhage, whereas …
Intra-Anterior Chamber Injection of Ranibizumab in Advanced Pediatric Vitreoretinal Diseases.
Zhang W, Liu H, Chen Y, Zhang X, Gu VY, Xiao H, Yang Y, Yin J, Peng J, Zhao P. Zhang W, et al. JAMA Ophthalmol. 2024 Feb 1;142(2):133-139. doi: 10.1001/jamaophthalmol.2023.6198. JAMA Ophthalmol. 2024. PMID: 38236592
The mean age was 4.6 years (range, 1 month to 9 years). Six patients were diagnosed with familial exudative vitreoretinopathy, 4 with morning glory syndrome, 1 with retinopathy of prematurity, and 2 with chronic retinal detachments of unknown causes. ...CONCL …
The mean age was 4.6 years (range, 1 month to 9 years). Six patients were diagnosed with familial exudative vitreoretinopat
Familial Exudative Vitreoretinopathy and Glaucoma: Observations, Insights, and Management Strategies.
Selvan H, Swamy DR, Temkar S, Venkatesh P, Gupta S. Selvan H, et al. J Glaucoma. 2018 Jan;27(1):e1-e6. doi: 10.1097/IJG.0000000000000810. J Glaucoma. 2018. PMID: 29088053
We report two cases of bilateral severe familial exudative vitreoretinopathy (FEVR) presenting with bilateral angle closure glaucoma, with evidence of neovascularization in one eye of each case. ...
We report two cases of bilateral severe familial exudative vitreoretinopathy (FEVR) presenting with bilateral angle clo …
Retinal capillary angioma in familial exudative vitreoretinopathy treated with photodynamic therapy.
Javellana JA, Drouilhet JH, Kokame GT, Chee PH, Wong BM. Javellana JA, et al. Am J Ophthalmol. 2004 Apr;137(4):780-2. doi: 10.1016/j.ajo.2003.10.001. Am J Ophthalmol. 2004. PMID: 15059735
PURPOSE: To report a case of familial exudative vitreoretinopathy with a retinal capillary angioma and persistent macular exudation treated with photodynamic therapy. ...CONCLUSION: Retinal capillary angioma may be present in association with familial
PURPOSE: To report a case of familial exudative vitreoretinopathy with a retinal capillary angioma and persistent macul …
Electroretinographic effects of retinal dragging and retinal folds in eyes with familial exudative vitreoretinopathy.
Yaguchi Y, Katagiri S, Fukushima Y, Yokoi T, Nishina S, Kondo M, Azuma N. Yaguchi Y, et al. Sci Rep. 2016 Jul 26;6:30523. doi: 10.1038/srep30523. Sci Rep. 2016. PMID: 27456314 Free PMC article. Clinical Trial.
We evaluated the retinal function of retinal dragging (Rdrag) and radial retinal folds (Rfolds) in eyes with familial exudative vitreoretinopathy (FEVR) using full-field electroretinography (ERG). ...
We evaluated the retinal function of retinal dragging (Rdrag) and radial retinal folds (Rfolds) in eyes with familial exudative
The Diagnostic Yield of Next Generation Sequencing in Inherited Retinal Diseases: A Systematic Review and Meta-analysis.
Britten-Jones AC, Gocuk SA, Goh KL, Huq A, Edwards TL, Ayton LN. Britten-Jones AC, et al. Am J Ophthalmol. 2023 May;249:57-73. doi: 10.1016/j.ajo.2022.12.027. Epub 2022 Dec 30. Am J Ophthalmol. 2023. PMID: 36592879 Review.
Ovid MEDLINE and Ovid Embase were searched on 6 June 2022. Clinical studies evaluating the diagnostic yield of NGS in individuals with IRDs were eligible for inclusion. ...The diagnostic yield of NGS was 61.3% (95% confidence interval: 57.8-64.7%; 51 studies) in mixed IRD …
Ovid MEDLINE and Ovid Embase were searched on 6 June 2022. Clinical studies evaluating the diagnostic yield of NGS in individuals wit …
28 results