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Quoted phrase not found in phrase index: "Exudative vitreoretinopathy 6"
Page 1
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 …
ETIOLOGY AND CLINICAL CHARACTERISTICS OF MACULAR EDEMA IN PATIENTS WITH FAMILIAL EXUDATIVE VITREORETINOPATHY.
Rao P, Lertjirachai I, Yonekawa Y, Hasbrook M, Thomas BJ, Wood EH, Mehta N, Mane G, Drenser KA, Trese MT, Capone A Jr. Rao P, et al. Retina. 2020 Jul;40(7):1367-1373. doi: 10.1097/IAE.0000000000002623. Retina. 2020. PMID: 31404032
PURPOSE: To describe the etiology and clinical characteristics of macular edema (ME) in patients with familial exudative vitreoretinopathy. METHODS: Observational, retrospective case series of 30 patients (34 eyes) with ME and familial exudative vit …
PURPOSE: To describe the etiology and clinical characteristics of macular edema (ME) in patients with familial exudative vitreoret …
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 …
PHOTODYNAMIC THERAPY-INDUCED ACUTE EXUDATIVE MACULOPATHY: Incidence, Clinical Features, and Long-Term Outcomes.
Manayath GJ, Ranjan R, Vidhate S, Narendran V. Manayath GJ, et al. Retina. 2020 Jan;40(1):135-144. doi: 10.1097/IAE.0000000000002343. Retina. 2020. PMID: 30312256
METHODS: This retrospective observational case series included all cases who developed massive serofibrinous macular exudation within a week after PDT. ...Photodynamic therapy-induced acute exudative maculopathy resolved to baseline or even better tomographic …
METHODS: This retrospective observational case series included all cases who developed massive serofibrinous macular exudation …
CLINICAL FEATURES AND SURGICAL OUTCOMES OF ENCIRCLING SCLERAL BUCKLING WITH CRYOTHERAPY IN FAMILIAL EXUDATIVE VITREORETINOPATHY-ASSOCIATED RHEGMATOGENOUS RETINAL DETACHMENT.
Huang L, Liang T, Lyu J, Jin H, Zhao P. Huang L, et al. Retina. 2022 Jan 1;42(1):55-63. doi: 10.1097/IAE.0000000000003280. Retina. 2022. PMID: 34393211
PURPOSE: To report the clinical features and surgical outcomes of encircling scleral buckling surgery with cryotherapy in familial exudative vitreoretinopathy (FEVR) patients with rhegmatogenous RD. ...RESULTS: There were 16 eyes with Stage 3A FEVR and eight eyes wi …
PURPOSE: To report the clinical features and surgical outcomes of encircling scleral buckling surgery with cryotherapy in familial exudat …
Signal Peptide Variants in Inherited Retinal Diseases: A Multi-Institutional Case Series.
Jimenez HJ, Procopio RA, Thuma TBT, Marra MH, Izquierdo N, Klufas MA, Nagiel A, Pennesi ME, Pulido JS. Jimenez HJ, et al. Int J Mol Sci. 2022 Nov 1;23(21):13361. doi: 10.3390/ijms232113361. Int J Mol Sci. 2022. PMID: 36362148 Free PMC article.
In silico evaluations were performed with MutPred, MutationTaster, and the signal peptide prediction tool, SignalP 6.0. SignalP 6.0 was further used to determine the locations of the three SP regions in each gene: the N-terminal region, hydrophobic core, and …
In silico evaluations were performed with MutPred, MutationTaster, and the signal peptide prediction tool, SignalP 6.0. Signal …
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder.
Sudnawa KK, Garber A, Cohen R, Calamia S, Kanner CH, Montes J, Bain JM, Fee RJ, Chung WK. Sudnawa KK, et al. Clin Genet. 2024 May;105(5):523-532. doi: 10.1111/cge.14487. Epub 2024 Jan 21. Clin Genet. 2024. PMID: 38247296
Visual problems included strabismus, hyperopia, and familial exudative vitreoretinopathy. Half of individuals walked without an assistive device. The mean Gross Motor Functional Measure-66 score was 56.6 (SD = 14.8). Average time to complete Nine-Hole …
Visual problems included strabismus, hyperopia, and familial exudative vitreoretinopathy. Half of individuals walked without a …
Update on the Phenotypic and Genotypic Spectrum of KIF11-Related Retinopathy.
Wang Y, Zhang Z, Huang L, Sun L, Li S, Zhang T, Ding X. Wang Y, et al. Genes (Basel). 2022 Apr 18;13(4):713. doi: 10.3390/genes13040713. Genes (Basel). 2022. PMID: 35456519 Free PMC article.
Background: This study aimed to report the frequency of KIF11-mutations in a large familial exudative vitreoretinopathy (FEVR) population, extend the clinical spectrum of KIF11-associated retinopathy and compare KIF11-associated retinopathy to FEVR with mutations in …
Background: This study aimed to report the frequency of KIF11-mutations in a large familial exudative vitreoretinopathy (FEVR) …
Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11.
Yang J, Xiao X, Li S, Mai G, Jia X, Wang P, Sun W, Zhang Q. Yang J, et al. Am J Ophthalmol. 2022 Mar;235:178-187. doi: 10.1016/j.ajo.2021.09.017. Epub 2021 Sep 25. Am J Ophthalmol. 2022. PMID: 34582765
RESULTS: A total of 55 potential pathogenic variants were identified, including 26 in KIF11 (28 families), 23 in NDP (25 families), and 6 in CTNNB1 (6 families). In total, 74 patients from the 59 families carried the variants, in whom clinical data were available fr …
RESULTS: A total of 55 potential pathogenic variants were identified, including 26 in KIF11 (28 families), 23 in NDP (25 families), and 6 …
Outcome and risk factors of vitreoretinal surgery in pediatric patients with familial exudative vitreoretinopathy.
El-Khoury S, Clement A, Chehaibou I, Abdelmassih Y, Edelson C, Metge F, Dureau P, Caputo G. El-Khoury S, et al. Graefes Arch Clin Exp Ophthalmol. 2020 Aug;258(8):1617-1623. doi: 10.1007/s00417-020-04712-w. Epub 2020 May 8. Graefes Arch Clin Exp Ophthalmol. 2020. PMID: 32385748
PURPOSE: To evaluate the outcome for vitreoretinal surgery in children with familial exudative vitreoretinopathy (FEVR) and to evaluate the risk factors associated with failure. ...Postoperatively, stages and VA improved significantly (p = 0.001; p = 0.04, respectiv …
PURPOSE: To evaluate the outcome for vitreoretinal surgery in children with familial exudative vitreoretinopathy (FEVR) and to …
52 results