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

Year Number of Results
1988 1
1991 1
1993 2
1995 1
1997 2
1998 3
1999 1
2001 1
2004 1
2006 1
2007 1
2009 1
2010 2
2011 1
2012 1
2013 1
2014 3
2015 3
2016 6
2017 11
2018 8
2019 11
2020 7
2021 7
2022 8
2023 7
2024 2

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80 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.
Neovascular glaucoma (NVG) is a type of secondary glaucoma, refractory to treatment, often incurable, with very poor visual prognosis. It is characterized by the appearance of new vessels over the iris and iridocorneal angle and frequently associates the presence of a fibr …
Neovascular glaucoma (NVG) is a type of secondary glaucoma, refractory to treatment, often incurable, with very poor visual prognosis …
Familial exudative vitreoretinopathy.
Benson WE. Benson WE. Trans Am Ophthalmol Soc. 1995;93:473-521. Trans Am Ophthalmol Soc. 1995. PMID: 8719692 Free PMC article.
RESULTS: Only 2 of 28 patients whose onset of symptoms was prior to their third birthday had a final visual acuity of 20/200 or better. Older patients had a better prognosis, because they were more likely to have asymmetrical retinal deterioration with only one eye deterio …
RESULTS: Only 2 of 28 patients whose onset of symptoms was prior to their third birthday had a final visual acuity of 20/200 or better. Olde …
EARLY-ONSET OF FAMILIAL EXUDATIVE VITREORETINOPATHY: Clinical Characteristics, Management, and Outcomes.
Kitic N, Chapron T, Metge-Galatoire F, Chehaibou I, Caputo G, Abdelmassih Y. Kitic N, et al. Retina. 2024 Apr 1;44(4):669-679. doi: 10.1097/IAE.0000000000004005. Retina. 2024. PMID: 37973048
CONCLUSION: Familial exudative vitreoretinopathy tended to be worse with earlier age at diagnosis, subsequently affecting the prognosis. Surgical intervention was common and primarily included lens-sparing vitrectomy and combined lensectomy and vitrectomy. ...
CONCLUSION: Familial exudative vitreoretinopathy tended to be worse with earlier age at diagnosis, subsequently affecting the prognosis …
Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene.
Seemab S, Pervaiz N, Zehra R, Anwar S, Bao Y, Abbasi AA. Seemab S, et al. BMC Evol Biol. 2019 Mar 8;19(1):72. doi: 10.1186/s12862-019-1400-9. BMC Evol Biol. 2019. PMID: 30849938 Free PMC article.
CONCLUSION: Taken together these results demonstrate that during the course of evolution, FZD4 has acquired new functions or epistasis via complex patter of gene duplications, sequence divergence and conformational remodeling. ...
CONCLUSION: Taken together these results demonstrate that during the course of evolution, FZD4 has acquired new functions or epistasi …
A systematic review of cases of West African crystalline maculopathy.
Abikoye TM, Idowu OO, Oluleye TS. Abikoye TM, et al. Int J Clin Pract. 2021 Dec;75(12):e14911. doi: 10.1111/ijcp.14911. Epub 2021 Sep 26. Int J Clin Pract. 2021. PMID: 34551184 Review.
Data reviewed included epidemiology, risk factors, clinical presentations, imaging characteristics, management and prognosis of WACM. Information on the location of the study was also extracted. ...Longitudinal studies, particularly in Africa, may be required to elucidate …
Data reviewed included epidemiology, risk factors, clinical presentations, imaging characteristics, management and prognosis of WACM. …
Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome.
Hoyek S, Wang M, Berrocal AM, Wong A, Place EM, Mason-Suares H, Lin AE, Mukai S, Patel NA. Hoyek S, et al. Ophthalmic Genet. 2023 Apr;44(2):198-203. doi: 10.1080/13816810.2022.2098987. Epub 2022 Jul 14. Ophthalmic Genet. 2023. PMID: 35834361
CONCLUSIONS: In premature neonates with atypical ROP, a clinical suspicion of concurrent FEVR or similar vasculopathy is important and genetic testing may elucidate a genetic etiology, which could influence management and prognosis. Turner syndrome can be connected with co …
CONCLUSIONS: In premature neonates with atypical ROP, a clinical suspicion of concurrent FEVR or similar vasculopathy is important and genet …
Five novel dysfunctional variants in the TSPAN12 gene in familial exudative vitreoretinopathy.
Wang Y, Lai Y, Jiang Z, Li S, Ding X. Wang Y, et al. Exp Eye Res. 2023 Sep;234:109574. doi: 10.1016/j.exer.2023.109574. Epub 2023 Jul 12. Exp Eye Res. 2023. PMID: 37451565
Low vision, high myopia, nystagmus, and leukocoria are the common symptom at the first presentation. All variants were also predicted as pathogenic in silico. Moreover, the luciferase assay demonstrated that all variants caused severely compromised Norrin/beta-catenin sign …
Low vision, high myopia, nystagmus, and leukocoria are the common symptom at the first presentation. All variants were also predicted …
Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease.
Liu J, Zhu J, Yang J, Zhang X, Zhang Q, Zhao P. Liu J, et al. Mol Genet Genomic Med. 2019 Jan;7(1):e00503. doi: 10.1002/mgg3.503. Epub 2018 Nov 25. Mol Genet Genomic Med. 2019. PMID: 30474316 Free PMC article.
METHODS: Amniocentesis and ultrasonography were performed in high-risk mothers, with children having FEVR or ND, to predict severe ocular abnormalities. RESULTS: Case 1: A homozygous NDP mutation (c.376T>C, NM_000266) was detected in the proband and his mother. ...CONCL …
METHODS: Amniocentesis and ultrasonography were performed in high-risk mothers, with children having FEVR or ND, to predict severe oc …
80 results