240 related articles for article (PubMed ID: 24084499)
1. High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy.
Kashani AH; Learned D; Nudleman E; Drenser KA; Capone A; Trese MT
Ophthalmology; 2014 Jan; 121(1):262-268. PubMed ID: 24084499
[TBL] [Abstract][Full Text] [Related]
2. Diversity of retinal vascular anomalies in patients with familial exudative vitreoretinopathy.
Kashani AH; Brown KT; Chang E; Drenser KA; Capone A; Trese MT
Ophthalmology; 2014 Nov; 121(11):2220-7. PubMed ID: 25005911
[TBL] [Abstract][Full Text] [Related]
3. Clinical and genetical features of probands and affected family members with familial exudative vitreoretinopathy in a large Chinese cohort.
Wang S; Zhang X; Hu Y; Fei P; Xu Y; Peng J; Zhao P
Br J Ophthalmol; 2021 Jan; 105(1):83-86. PubMed ID: 32238352
[TBL] [Abstract][Full Text] [Related]
4. Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.
Seo SH; Yu YS; Park SW; Kim JH; Kim HK; Cho SI; Park H; Lee SJ; Seong MW; Park SS; Kim JY
Invest Ophthalmol Vis Sci; 2015 Aug; 56(9):5143-51. PubMed ID: 26244290
[TBL] [Abstract][Full Text] [Related]
5. The spectrum of genetic mutations in patients with asymptomatic mild familial exudative vitreoretinopathy.
Chen C; Sun L; Li S; Huang L; Zhang T; Wang Z; Yu B; Ding X
Exp Eye Res; 2020 Mar; 192():107941. PubMed ID: 31987760
[TBL] [Abstract][Full Text] [Related]
6. The characteristics of digenic familial exudative vitreoretinopathy.
Li Y; Peng J; Li J; Zhang Q; Li J; Zhang X; Fei P; She K; Zhao P
Graefes Arch Clin Exp Ophthalmol; 2018 Nov; 256(11):2149-2156. PubMed ID: 30097784
[TBL] [Abstract][Full Text] [Related]
7. Familial Exudative Vitreoretinopathy: Spectral-Domain Optical Coherence Tomography of the Vitreoretinal Interface, Retina, and Choroid.
Yonekawa Y; Thomas BJ; Drenser KA; Trese MT; Capone A
Ophthalmology; 2015 Nov; 122(11):2270-7. PubMed ID: 26299697
[TBL] [Abstract][Full Text] [Related]
8. Optical Coherence Tomography Angiography in Familial Exudative Vitreoretinopathy: Clinical Features and Phenotype-Genotype Correlation.
Chen C; Liu C; Wang Z; Sun L; Zhao X; Li S; Luo X; Zhang A; Chong V; Lu L; Ding X
Invest Ophthalmol Vis Sci; 2018 Dec; 59(15):5726-5734. PubMed ID: 30513533
[TBL] [Abstract][Full Text] [Related]
9. Whole exome sequencing revealed 14 variants in NDP, FZD4, LRP5, and TSPAN12 genes for 20 families with familial exudative vitreoretinopathy.
Dan H; Wang D; Huang Z; Shi Q; Zheng M; Xiao Y; Song Z
BMC Med Genomics; 2022 Mar; 15(1):54. PubMed ID: 35277167
[TBL] [Abstract][Full Text] [Related]
10. Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12.
Schatz P; Khan AO
Acta Ophthalmol; 2017 Nov; 95(7):705-709. PubMed ID: 28211206
[TBL] [Abstract][Full Text] [Related]
11. Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy.
Li JK; Li Y; Zhang X; Chen CL; Rao YQ; Fei P; Zhang Q; Zhao P; Li J
Invest Ophthalmol Vis Sci; 2018 Nov; 59(13):5368-5381. PubMed ID: 30452590
[TBL] [Abstract][Full Text] [Related]
12. Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.
Xu Y; Huang L; Li J; Zhang Q; Fei P; Zhu X; Tai Z; Ma S; Gong B; Li Y; Zang W; Zhu X; Zhao P; Yang Z
Mol Vis; 2014; 20():1296-306. PubMed ID: 25352738
[TBL] [Abstract][Full Text] [Related]
13. 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
Ann Med; 2022 Dec; 54(1):3286-3298. PubMed ID: 36411543
[TBL] [Abstract][Full Text] [Related]
14. Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR.
Trang DT; Phu NM; Hung DM; Nhung VP; Ha NN; Thuong MTH; Ngoc TTB; Hiep NX; Ton ND; Hai NV; Ha NH
Mol Vis; 2022; 28():480-491. PubMed ID: 37089697
[TBL] [Abstract][Full Text] [Related]
15. Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
Rao FQ; Cai XB; Cheng FF; Cheng W; Fang XL; Li N; Huang XF; Li LH; Jin ZB
Invest Ophthalmol Vis Sci; 2017 May; 58(5):2623-2629. PubMed ID: 28494495
[TBL] [Abstract][Full Text] [Related]
16. Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR).
Seo SH; Kim MJ; Park SW; Kim JH; Yu YS; Song JY; Cho SI; Ahn JH; Oh YH; Lee JS; Lee S; Seong MW; Park SS; Kim JY
Invest Ophthalmol Vis Sci; 2016 Dec; 57(15):6902-6908. PubMed ID: 28002565
[TBL] [Abstract][Full Text] [Related]
17. Symmetry of folds in FEVR: A genotype-phenotype correlation study.
Wang Z; Chen C; Sun L; Zhang A; Liu C; Huang L; Ding X
Exp Eye Res; 2019 Sep; 186():107720. PubMed ID: 31299183
[TBL] [Abstract][Full Text] [Related]
18. Variable reduction in Norrin signaling activity caused by novel mutations in
Tian T; Zhang X; Zhang Q; Zhao P
Mol Vis; 2019; 25():60-69. PubMed ID: 30820142
[TBL] [Abstract][Full Text] [Related]
19. Mutation Spectrum of the LRP5, NDP, and TSPAN12 Genes in Chinese Patients With Familial Exudative Vitreoretinopathy.
Tang M; Sun L; Hu A; Yuan M; Yang Y; Peng X; Ding X
Invest Ophthalmol Vis Sci; 2017 Nov; 58(13):5949-5957. PubMed ID: 29181528
[TBL] [Abstract][Full Text] [Related]
20. Novel mutation in
Song Z; Li M; Wang C; Wang Y; Zhang L; Li N; Yang R; Sun P
Ophthalmic Genet; 2022 Feb; 43(1):104-109. PubMed ID: 34445920
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]