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Quoted phrase not found in phrase index: "Exudative vitreoretinopathy 5"
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.
Abbreviations: NVG = neovascular glaucoma, ICA = iridocorneal angle, IOP = intraocular pressure, TM = trabecular meshwork, AH = aqueous humor, AC = anterior chamber, PRP = panretinal photocoagulation, VEGF = vascular endothelial growing factor, Anti-VEGF = anti- vascular endothel …
Abbreviations: NVG = neovascular glaucoma, ICA = iridocorneal angle, IOP = intraocular pressure, TM = trabecular meshwork, AH = aqueous humo …
Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy.
Tao T, Xu N, Li J, Li H, Qu J, Yin H, Liang J, Zhao M, Li X, Huang L. Tao T, et al. Invest Ophthalmol Vis Sci. 2021 Dec 1;62(15):4. doi: 10.1167/iovs.62.15.4. Invest Ophthalmol Vis Sci. 2021. PMID: 34860240 Free PMC article.
PURPOSE: To investigate the clinical findings in Chinese patients diagnosed with familial exudative vitreoretinopathy (FEVR) and carrying pathogenic mutations. ...Patients with LRP5, FZD4, TSPAN12, or NDP mutations were mainly classified into stage 4 and stage 5 …
PURPOSE: To investigate the clinical findings in Chinese patients diagnosed with familial exudative vitreoretinopathy (FEVR) a …
Coats-like Exudative Vitreoretinopathy in Retinitis Pigmentosa: Ocular Manifestations and Treatment Outcomes.
Moinuddin O, Sathrasala S, Jayasundera KT, Branham KH, Chang EY, Qian CX, Recchia FM, Fahim AT, Besirli CG. Moinuddin O, et al. Ophthalmol Retina. 2021 Jan;5(1):86-96. doi: 10.1016/j.oret.2020.03.026. Epub 2020 Apr 9. Ophthalmol Retina. 2021. PMID: 32507488 Free PMC article.
PARTICIPANTS: Patients with a diagnosis of RP demonstrating Coats-like exudative vitreoretinopathy between January 1, 2008, and October 1, 2019. ...RESULTS: Nine patients diagnosed with RP and demonstrating Coats-like exudative vitreoretinopathy were i …
PARTICIPANTS: Patients with a diagnosis of RP demonstrating Coats-like exudative vitreoretinopathy between January 1, 2008, an …
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.
SUMMARY: Herein are current reviews of a variety of ophthalmologic genetic disorders such as anophthalmia, aniridia, albinism, anterior segment dysgenesis, Marfan syndrome, ectopia lentis, neurofibromatosis, retinal hemangioblastomas, and familial exudative vitreoretino …
SUMMARY: Herein are current reviews of a variety of ophthalmologic genetic disorders such as anophthalmia, aniridia, albinism, anterior segm …
Refractive Status and Biometric Characteristics of Children With Familial Exudative Vitreoretinopathy.
Hu Y, Fan Z, Zhao X, Correa VSMC, Wu Z, Lu X, Zeng X, Chen L, Yu Z, Zheng L, He J, Zhang G. Hu Y, et al. Invest Ophthalmol Vis Sci. 2023 Oct 3;64(13):27. doi: 10.1167/iovs.64.13.27. Invest Ophthalmol Vis Sci. 2023. PMID: 37850946 Free PMC article.
PURPOSE: To compare biometric characteristics between patients with early-stage familial exudative vitreoretinopathy (FEVR) and healthy controls. METHODS: This case-control study included 50 FEVR eyes in stage 1-2 and 50 control eyes matched by age, gender and spher …
PURPOSE: To compare biometric characteristics between patients with early-stage familial exudative vitreoretinopathy (FEVR) an …
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With Microcephaly.
Hull S, Arno G, Ostergaard P, Pontikos N, Robson AG, Webster AR, Hogg CR, Wright GA, Henderson RHH, Martin CA, Jackson AP, Mansour S, Moore AT, Michaelides M. Hull S, et al. Am J Ophthalmol. 2019 Nov;207:87-98. doi: 10.1016/j.ajo.2019.05.001. Epub 2019 May 8. Am J Ophthalmol. 2019. PMID: 31077665 Free article.
PURPOSE: Familial exudative vitreoretinopathy (FEVR) is a rare finding in patients with genetic forms of microcephaly. ...
PURPOSE: Familial exudative vitreoretinopathy (FEVR) is a rare finding in patients with genetic forms of microcephaly. ...
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
PURPOSE: To describe the clinical characteristics, management, and outcomes of toddlers (under the age of 3) diagnosed with familial exudative vitreoretinopathy. METHODS: In this retrospective study, patients diagnosed with familial exudative vitreoretinop …
PURPOSE: To describe the clinical characteristics, management, and outcomes of toddlers (under the age of 3) diagnosed with familial exud …
Genetic Characteristics and Clinical Manifestations of Foveal Hypoplasia in Familial Exudative Vitreoretinopathy.
Ju Y, Zhang L, Gao F, Zong Y, Chen T, Ruan L, Chang Q, Zhang T, Huang X. Ju Y, et al. Am J Ophthalmol. 2024 Jun;262:73-85. doi: 10.1016/j.ajo.2024.01.029. Epub 2024 Jan 26. Am J Ophthalmol. 2024. PMID: 38280677
PURPOSE: This study aimed to ascertain the occurrence of foveal hypoplasia (FH) in individuals diagnosed with familial exudative vitreoretinopathy (FEVR). DESIGN: Retrospective cohort study. ...
PURPOSE: This study aimed to ascertain the occurrence of foveal hypoplasia (FH) in individuals diagnosed with familial exudative v …
Novel variants in familial exudative vitreoretinopathy patients with KIF11 mutations and the Genotype-Phenotype correlation.
Chen C, Sun L, Li S, Huang L, Zhang T, Wang Z, Yu B, Luo X, Ding X. Chen C, et al. Exp Eye Res. 2020 Oct;199:108165. doi: 10.1016/j.exer.2020.108165. Epub 2020 Jul 28. Exp Eye Res. 2020. PMID: 32730767
Familial exudative vitreoretinopathy (FEVR) is an inherited disease characterized by abnormal development of retinal vasculature. ...Six of the probands were detected to have microcephaly. In conclusion: Most (5/9,55.6%) of the causative mutations were frames …
Familial exudative vitreoretinopathy (FEVR) is an inherited disease characterized by abnormal development of retinal vasculatu …
Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.
Mao J, Chen Y, Fang Y, Shao Y, Xiang Z, Li H, Zhao S, Chen Y, Shen L. Mao J, et al. Ann Med. 2022 Dec;54(1):3286-3298. doi: 10.1080/07853890.2022.2146744. Ann Med. 2022. PMID: 36411543 Free PMC article.
OBJECTIVE: To explore the clinical manifestations and search for the variants of six related genes (LRP5, FZD4, TSPAN12, NDP, KIF11 and ZNF408) in Chinese patients with familial exudative vitreoretinopathy (FEVR), and investigate the correlation between the genetic …
OBJECTIVE: To explore the clinical manifestations and search for the variants of six related genes (LRP5, FZD4, TSPAN12, NDP, KIF11 and ZNF4 …
129 results