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Year Number of Results
1995 1
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2003 1
2005 1
2009 1
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2019 1
2021 2
2022 1
2023 2
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12 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.
Managing the NVG we should aim to: 1) reduce ocular ischemia and treat its underlying cause, 2) reduce elevated IOP, once installed and 3) control the inflammatory process. Anyway, the best treatment is prevention, so we must be very attentive at patients with risk factors …
Managing the NVG we should aim to: 1) reduce ocular ischemia and treat its underlying cause, 2) reduce elevated IOP, once installed and 3
SNPs: impact on gene function and phenotype.
Shastry BS. Shastry BS. Methods Mol Biol. 2009;578:3-22. doi: 10.1007/978-1-60327-411-1_1. Methods Mol Biol. 2009. PMID: 19768584 Review.
To illustrate the effect of SNPs on gene function and phenotype, this minireview focuses on evidences revealing the impact of SNPs on the development and progression of three human eye disorders (Norrie disease, familial exudative vitreoretinopathy, and retinopathy …
To illustrate the effect of SNPs on gene function and phenotype, this minireview focuses on evidences revealing the impact of SNPs on the de …
Familial Exudative Vitreoretinopathy: Pathophysiology, Diagnosis, and Management.
Tauqeer Z, Yonekawa Y. Tauqeer Z, et al. Asia Pac J Ophthalmol (Phila). 2018 May-Jun;7(3):176-182. doi: 10.22608/APO.201855. Epub 2018 Apr 9. Asia Pac J Ophthalmol (Phila). 2018. PMID: 29633588 Free article. Review.
Familial exudative vitreoretinopathy (FEVR) is a heritable vitreoretinopathy characterized by anomalous retinal vascular development. ...Further studies are underway to better characterize this complex vitreoretinopathy....
Familial exudative vitreoretinopathy (FEVR) is a heritable vitreoretinopathy characterized by anomalous retinal vascula …
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.
Most studies (90 studies) used targeted gene panels. The diagnostic yield of NGS was 61.3% (95% confidence interval: 57.8-64.7%; 51 studies) in mixed IRD phenotypes, 58.2% (51.6-64.6%; 41 studies) in rod-cone dystrophies, 57.7% (46.8-68.3%; eight studies) in macular …
Most studies (90 studies) used targeted gene panels. The diagnostic yield of NGS was 61.3% (95% confidence interval: 57.8-64.7%; 51 s …
Etiologies and clinical characteristics of young patients with angle-closure glaucoma: a 15-year single-center retrospective study.
Gao F, Wang J, Chen J, Wang X, Chen Y, Sun X. Gao F, et al. Graefes Arch Clin Exp Ophthalmol. 2021 Aug;259(8):2379-2387. doi: 10.1007/s00417-021-05172-6. Epub 2021 Apr 19. Graefes Arch Clin Exp Ophthalmol. 2021. PMID: 33876278 Free PMC article. Review.
RESULTS: A total of 298 patients (463 eyes) met the criteria, including 153 females (51.3%) and 145 males (48.7%); the mean age was 25.6 13.0 years. Primary angle-closure glaucoma (PACG), uveitis, and anterior segment dysgenesis (ASD) were the top three etiologies in our p …
RESULTS: A total of 298 patients (463 eyes) met the criteria, including 153 females (51.3%) and 145 males (48.7%); the mean age was 2 …
Molecular dissection of Norrie disease.
Berger W. Berger W. Acta Anat (Basel). 1998;162(2-3):95-100. doi: 10.1159/000046473. Acta Anat (Basel). 1998. PMID: 9831755 Review.
Numerous point mutations in this gene have been identified in three distinct clinical entities: (1) ND, (2) familial and sporadic exudative vitreoretinopathy, and (3) retinopathy of prematurity. The gene encodes a relatively small protein, consisting of 133 a …
Numerous point mutations in this gene have been identified in three distinct clinical entities: (1) ND, (2) familial and sporadic exudati
How to interpret a healthcare economic analysis.
Brown MM, Brown GC. Brown MM, et al. Curr Opin Ophthalmol. 2005 Jun;16(3):191-4. Curr Opin Ophthalmol. 2005. PMID: 15870578 Review.
RECENT FINDINGS: There are four variants of healthcare economic analyses: (1) cost-minimization analysis; (2) cost-benefit analysis; (3) cost-effectiveness analysis and (4) cost-utility analysis. Cost-utility utility analysis has assumed an increasingly important role in h …
RECENT FINDINGS: There are four variants of healthcare economic analyses: (1) cost-minimization analysis; (2) cost-benefit analysis; (3
Norrie disease and MAO genes: nearest neighbors.
Chen ZY, Denney RM, Breakefield XO. Chen ZY, et al. Hum Mol Genet. 1995;4 Spec No:1729-37. doi: 10.1093/hmg/4.suppl_1.1729. Hum Mol Genet. 1995. PMID: 8541872 Review.
The Norrie disease and MAO genes are tandemly arranged in the p11.4-p11.3 region of the human X chromosome in the order tel-MAOA-MAOB-NDP-cent. ...Other mutations in the NDP gene have been found to underlie another X-linked eye disease, exudative vitreo-retinopathy. …
The Norrie disease and MAO genes are tandemly arranged in the p11.4-p11.3 region of the human X chromosome in the order tel-MAOA-MAOB …
Clinical evidence of intravitreal triamcinolone acetonide in the management of age-related macular degeneration.
Becerra EM, Morescalchi F, Gandolfo F, Danzi P, Nascimbeni G, Arcidiacono B, Semeraro F. Becerra EM, et al. Curr Drug Targets. 2011 Feb;12(2):149-72. doi: 10.2174/138945011794182746. Curr Drug Targets. 2011. PMID: 20887246 Review.
The first experiences with IVTA as monotherapy for the treatment of exudative AMD reported a positive outcome in transiently reducing the leakage from CNV. ...A question remains open on whether a combination treatment with anti-VEGF, triamcinolone and/or PDT may be a treat …
The first experiences with IVTA as monotherapy for the treatment of exudative AMD reported a positive outcome in transiently reducing …
12 results