BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 25828824)

  • 1. A case of familial exudative vitreoretinopathy identified after genetic testing.
    Miller KE; Willis MJ; McClatchey SK
    J AAPOS; 2015 Apr; 19(2):178-80. PubMed ID: 25828824
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Simultaneous Novel Mutations of LRP5 and TSPAN12 in a Case of Familial Exudative Vitreoretinopathy.
    Kramer GD; Say EA; Shields CL
    J Pediatr Ophthalmol Strabismus; 2016 Feb; 53 Online():e1-5. PubMed ID: 27007396
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FAMILIAL EXUDATIVE VITREOTINOPATHY-LIKE FEATURES IN STICKLER TYPE IV ASSOCIATED WITH NOVEL VARIANTS IN COL9A1.
    Alsubaie HF; Magliyah MS; AlRaddadi O; AlZaid A; Nowilaty SR
    Retin Cases Brief Rep; 2023 Mar; 17(2):206-211. PubMed ID: 33973556
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. 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]  

  • 6. Serpiginous Intraretinal Lesions Associated With Familial Exudative Vitreoretinopathy.
    Güemes-Villahoz N; Acón D; Hamichi SE; Tanenbaum R; Berrocal AM
    Ophthalmic Surg Lasers Imaging Retina; 2021 Mar; 52(3):155-159. PubMed ID: 34038691
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mirror image of familial exudative vitreoretinopathy in identical twins.
    Teke MY; Tekin K; Aydemir E; Yavrum F
    Int Ophthalmol; 2019 Apr; 39(4):935-941. PubMed ID: 29492729
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. A family harboring homozygous FZD4 deletion supports the existence of recessive FZD4-related familial exudative vitreoretinopathy.
    Khan AO; Lenzner S; Bolz HJ
    Ophthalmic Genet; 2017; 38(4):380-382. PubMed ID: 27668459
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Familial exudative vitreoretinopathy caused by a homozygous mutation in TSPAN12 in a cystic fibrosis infant.
    Savarese M; Spinelli E; Gandolfo F; Lemma V; Di Fruscio G; Padoan R; Morescalchi F; D'Agostino M; Savoldi G; Semeraro F; Nigro V; Bonatti S
    Ophthalmic Genet; 2014 Sep; 35(3):184-6. PubMed ID: 23834558
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DISTINCTIVE WHITE FUNDUS LESIONS IN FAMILIAL EXUDATIVE VITREORETINOPATHY: A NEWLY CHARACTERIZED CLINICAL FEATURE.
    Johnson BB; Hubbard GB; Mendoza PR; Grossniklaus HE
    Retin Cases Brief Rep; 2017 Fall; 11(4):291-295. PubMed ID: 27648585
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 44(2):171-174. PubMed ID: 32530348
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel variant in the
    Elhusseiny AM; Jabroun M; Rajabi F; Gonzalez E; Alkharashi M
    Eur J Ophthalmol; 2022 Nov; 32(6):NP6-NP9. PubMed ID: 34151585
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP).
    López-Cañizares A; Lazzarini TA; Mendoza C; Berrocal AM
    Ophthalmic Genet; 2023 Jun; 44(3):313-317. PubMed ID: 36444989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.