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Journal Abstract Search

194 related items for PubMed ID: 34038691

  • 1.
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  • 2. Coats-Like Presentation of Familial Exudative Vitreoretinopathy Associated With a Novel LRP5 Variant.
    López-Font FJ, Shah SM, Lin BR, Cruz NFSD, Sengillo JD, Berrocal AM.
    Ophthalmic Surg Lasers Imaging Retina; 2024 Aug; 55(8):462-466. PubMed ID: 38752919
    [Abstract] [Full Text] [Related]

  • 3. 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 03; 59(15):5726-5734. PubMed ID: 30513533
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  • 4. Macular Hole Complicating Familial Exudative Vitreoretinopathy Due to LRP5 Mutation in an Adolescent.
    Munier FL, Daruich A.
    Ophthalmic Surg Lasers Imaging Retina; 2019 Feb 01; 50(2):e49-e51. PubMed ID: 30768230
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  • 5. 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.
    Am J Ophthalmol; 2024 Jun 01; 262():73-85. PubMed ID: 38280677
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  • 6. Familial exudative vitreoretinopathy (FEVR) in a child with a Jagged 1 variant identified on genetic testing.
    Hucko L, da Cruz NFS, Staropoli P, Berrocal AM.
    Ophthalmic Genet; 2024 Oct 01; 45(5):488-493. PubMed ID: 38836470
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  • 8. Planned Preterm Delivery and Treatment of Severe Infantile FEVR With Osteoporosis-Pseudoglioma Syndrome.
    Ebert JJ, Utz VM, Hartnett ME, Tiao G, Sisk RA.
    Ophthalmic Surg Lasers Imaging Retina; 2022 Apr 01; 53(4):228-232. PubMed ID: 35417292
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  • 9. 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 01; 54(1):3286-3298. PubMed ID: 36411543
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  • 11. Unrecognized ROPER in a child with a novel pathogenic variant in ZNF408 gene.
    Tanenbaum R, Acon D, El Hamichi S, Negron C, Berrocal AM.
    Ophthalmic Genet; 2023 Apr 01; 44(2):171-174. PubMed ID: 32530348
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  • 14. Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12.
    Schatz P, Khan AO.
    Acta Ophthalmol; 2017 Nov 01; 95(7):705-709. PubMed ID: 28211206
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  • 15. Familial Exudative Vitreoretinopathy With Neurodevelopmental Delay and Hypoplasia of the Corpus Callosum.
    Amorelli GM, Barresi C, Ji MH, Orazi L, Molle F, Lepore D.
    Ophthalmic Surg Lasers Imaging Retina; 2020 Oct 01; 51(10):588-591. PubMed ID: 33104226
    [Abstract] [Full Text] [Related]

  • 16. Mirror image of familial exudative vitreoretinopathy in identical twins.
    Teke MY, Tekin K, Aydemir E, Yavrum F.
    Int Ophthalmol; 2019 Apr 01; 39(4):935-941. PubMed ID: 29492729
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  • 17. A Novel Pathogenic Variant in NDP Gene With Incomplete Penetrance Manifests as X-Linked Familial Exudative Vitreoretinopathy.
    Scott NL, Tran KD, Russell JF, Hinkle JW, Cernichiaro-Espinosa LA, Lauer A, Berrocal AM.
    Ophthalmic Surg Lasers Imaging Retina; 2019 Feb 01; 50(2):120-124. PubMed ID: 30768221
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  • 18. Novel mutation in TSPAN12 associated with familial exudative vitreoretinopathy in a Chinese pedigree.
    Song Z, Li M, Wang C, Wang Y, Zhang L, Li N, Yang R, Sun P.
    Ophthalmic Genet; 2022 Feb 01; 43(1):104-109. PubMed ID: 34445920
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  • 19. Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy.
    Lin Y, Gao H, Chen C, Zhu Y, Li T, Liu B, Ma C, Jiang H, Li Y, Huang Y, Wu Q, Li H, Liang X, Jin C, Ye J, Huang X, Lu L.
    Int J Mol Med; 2018 Feb 01; 41(2):773-782. PubMed ID: 29207047
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  • 20. A Novel Variant of the FZD4 Gene in a Chinese Family Causes Autosomal Dominant Familial Exudative Vitreoretinopathy.
    Yang L, Fu J, Cheng J, Wei C, Zhou Q, Ijaz I, Lv H, Fu J.
    Cell Physiol Biochem; 2018 Feb 01; 51(5):2445-2455. PubMed ID: 30537745
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