BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 24397708)

  • 1. Sorting out co-occurrence of rare monogenic retinopathies: Stargardt disease co-existing with congenital stationary night blindness.
    Huynh N; Jeffrey BG; Turriff A; Sieving PA; Cukras CA
    Ophthalmic Genet; 2014 Mar; 35(1):51-6. PubMed ID: 24397708
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Retinal phenotypic characterization of patients with
    López-Rubio S; Chacon-Camacho OF; Matsui R; Guadarrama-Vallejo D; Astiazarán MC; Zenteno JC
    Mol Vis; 2018; 24():105-114. PubMed ID: 29422768
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar Cells.
    Smirnov VM; Robert MP; Condroyer C; Navarro J; Antonio A; Rozet JM; Sahel JA; Perrault I; Audo I; Zeitz C
    JAMA Ophthalmol; 2022 Dec; 140(12):1163-1173. PubMed ID: 36264558
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Full-field ERG as a predictor of the natural course of
    Schroeder M; Kjellström U
    Mol Vis; 2018; 24():1-16. PubMed ID: 29386879
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
    Burke TR; Fishman GA; Zernant J; Schubert C; Tsang SH; Smith RT; Ayyagari R; Koenekoop RK; Umfress A; Ciccarelli ML; Baldi A; Iannaccone A; Cremers FP; Klaver CC; Allikmets R
    Invest Ophthalmol Vis Sci; 2012 Jul; 53(8):4458-67. PubMed ID: 22661473
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa.
    Chen RW; Greenberg JP; Lazow MA; Ramachandran R; Lima LH; Hwang JC; Schubert C; Braunstein A; Allikmets R; Tsang SH
    Am J Ophthalmol; 2012 Jan; 153(1):143-54.e2. PubMed ID: 21920492
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Early-onset stargardt disease: phenotypic and genotypic characteristics.
    Lambertus S; van Huet RA; Bax NM; Hoefsloot LH; Cremers FP; Boon CJ; Klevering BJ; Hoyng CB
    Ophthalmology; 2015 Feb; 122(2):335-44. PubMed ID: 25444351
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expanding the Mutation Spectrum in
    Nassisi M; Mohand-Saïd S; Dhaenens CM; Boyard F; Démontant V; Andrieu C; Antonio A; Condroyer C; Foussard M; Méjécase C; Eandi CM; Sahel JA; Zeitz C; Audo I
    Int J Mol Sci; 2018 Jul; 19(8):. PubMed ID: 30060493
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.
    Testa F; Rossi S; Sodi A; Passerini I; Di Iorio V; Della Corte M; Banfi S; Surace EM; Menchini U; Auricchio A; Simonelli F
    Invest Ophthalmol Vis Sci; 2012 Jul; 53(8):4409-15. PubMed ID: 22661472
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and molecular characteristics of childhood-onset Stargardt disease.
    Fujinami K; Zernant J; Chana RK; Wright GA; Tsunoda K; Ozawa Y; Tsubota K; Robson AG; Holder GE; Allikmets R; Michaelides M; Moore AT
    Ophthalmology; 2015 Feb; 122(2):326-34. PubMed ID: 25312043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt Disease.
    Lee W; Zernant J; Nagasaki T; Tsang SH; Allikmets R
    Am J Ophthalmol; 2018 Nov; 195():16-25. PubMed ID: 30055151
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The absence of fundus abnormalities in Stargardt disease.
    Bax NM; Lambertus S; Cremers FPM; Klevering BJ; Hoyng CB
    Graefes Arch Clin Exp Ophthalmol; 2019 Jun; 257(6):1147-1157. PubMed ID: 30903310
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New insights into Stargardt disease with multimodal imaging.
    Pang CE; Suqin Y; Sherman J; Freund KB
    Ophthalmic Surg Lasers Imaging Retina; 2015 Feb; 46(2):257-61. PubMed ID: 25707054
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Disruption in Bruch membrane in patients with Stargardt disease.
    Park SP; Chang S; Allikmets R; Smith RT; Burke TR; Gregory-Roberts E; Tsang SH
    Ophthalmic Genet; 2012 Mar; 33(1):49-52. PubMed ID: 22060670
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease.
    Sangermano R; Bax NM; Bauwens M; van den Born LI; De Baere E; Garanto A; Collin RW; Goercharn-Ramlal AS; den Engelsman-van Dijk AH; Rohrschneider K; Hoyng CB; Cremers FP; Albert S
    Ophthalmology; 2016 Jun; 123(6):1375-85. PubMed ID: 26976702
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Additional evidence supports GRM6 p.Thr178Met as a cause of congenital stationary night blindness in three horse breeds.
    Esdaile E; Knickelbein KE; Donnelly CG; Ferneding M; Motta MJ; Story BD; Avila F; Finno CJ; Gilger BC; Sandmeyer L; Thomasy S; Bellone RR
    Vet Ophthalmol; 2024 May; 27(3):248-255. PubMed ID: 37815029
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early impairment of the full-field photopic negative response in patients with Stargardt disease and pathogenic variants of the ABCA4 gene.
    Abed E; Placidi G; Campagna F; Federici M; Minnella A; Guerri G; Bertelli M; Piccardi M; Galli-Resta L; Falsini B
    Clin Exp Ophthalmol; 2018 Jul; 46(5):519-530. PubMed ID: 29178665
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Double hyperautofluorescent ring on fundus autofluorescence in ABCA4.
    Abalem MF; Qian CX; Branham K; Schlegel D; Fahim AT; Khan NW; Heckenlively JR; Jayasundera KT
    Ophthalmic Genet; 2018; 39(1):87-91. PubMed ID: 28726568
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical phenotypes and prognostic full-field electroretinographic findings in Stargardt disease.
    Zahid S; Jayasundera T; Rhoades W; Branham K; Khan N; Niziol LM; Musch DC; Heckenlively JR
    Am J Ophthalmol; 2013 Mar; 155(3):465-473.e3. PubMed ID: 23219216
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The clinical effect of homozygous ABCA4 alleles in 18 patients.
    Fujinami K; Sergouniotis PI; Davidson AE; Mackay DS; Tsunoda K; Tsubota K; Robson AG; Holder GE; Moore AT; Michaelides M; Webster AR
    Ophthalmology; 2013 Nov; 120(11):2324-31. PubMed ID: 23769331
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.