BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 26967979)

  • 1. CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype.
    Dixon MW; Stem MS; Schuette JL; Keegan CE; Besirli CG
    Ophthalmic Genet; 2016 Dec; 37(4):468-470. PubMed ID: 26967979
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial Exudative Vitreoretinopathy and Systemic Abnormalities in Patients With CTNNB1 Mutations.
    Huang L; Lu J; Wang Y; Sun L; Ding X
    Invest Ophthalmol Vis Sci; 2023 Feb; 64(2):18. PubMed ID: 36790797
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Vitreous hemorrhage as the initial manifestation of familial exudative vitreoretinopathy in an eight-year-old child].
    Benoist D'azy C; Bonnin N; Maurin C; Farguette F; Chiambaretta F
    J Fr Ophtalmol; 2016 Jun; 39(6):549-53. PubMed ID: 27230891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel truncating variants in
    He Y; Yang M; Zhao R; Peng L; Dai E; Huang L; Zhao P; Li S; Yang Z
    J Med Genet; 2023 Feb; 60(2):174-182. PubMed ID: 35361685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial Exudative Vitreoretinopathy With a Novel LRP5 Mutation.
    Pefkianaki M; Hasanreisoglu M; Suchy SF; Shields CL
    J Pediatr Ophthalmol Strabismus; 2016 Jul; 53():e39-42. PubMed ID: 27486893
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Familial exudative vitreoretinopathy].
    Peng X; Wang G; Zhang F
    Zhonghua Yan Ke Za Zhi; 1995 Nov; 31(6):426-9. PubMed ID: 8762569
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial Exudative Vitreoretinopathy: Presentation in the First Week of Life.
    Chawla R; Bypareddy R; Chandra P; Vohra R
    J Pediatr Ophthalmol Strabismus; 2015; 52(5):317-8. PubMed ID: 26431558
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
    Panagiotou ES; Sanjurjo Soriano C; Poulter JA; Lord EC; Dzulova D; Kondo H; Hiyoshi A; Chung BH; Chu YW; Lai CHY; Tafoya ME; Karjosukarso D; Collin RWJ; Topping J; Downey LM; Ali M; Inglehearn CF; Toomes C
    Am J Hum Genet; 2017 Jun; 100(6):960-968. PubMed ID: 28575650
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy.
    Peng Y; Zhao R; Dai E; Peng L; He Y; Li S; Yang M
    Eur J Ophthalmol; 2022 Nov; 32(6):3220-3226. PubMed ID: 35037517
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Novel mutation in
    Coussa RG; Zhao Y; DeBenedictis MJ; Babiuch A; Sears J; Traboulsi EI
    Ophthalmic Genet; 2020 Feb; 41(1):63-68. PubMed ID: 32039639
    [No Abstract]   [Full Text] [Related]  

  • 14. Association of autosomal dominant familial exudative vitreoretinopathy and spinal muscular atrophy.
    Mammo D; Yonekawa Y; Thomas BJ; Shah AR; Abbey AM; Trese MT; Drenser KA; Capone A
    Eur J Ophthalmol; 2015 Oct; 25(6):e116-8. PubMed ID: 26109022
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Familial Exudative Vitreoretinopathy.
    Chen KJ; Wang NK; Wu WC
    JAMA Ophthalmol; 2017 Apr; 135(4):e165487. PubMed ID: 28418565
    [No Abstract]   [Full Text] [Related]  

  • 17. Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR.
    Musada GR; Jalali S; Hussain A; Chururu AR; Gaddam PR; Chakrabarti S; Kaur I
    Mol Vis; 2016; 22():491-502. PubMed ID: 27217716
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.