BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 37748682)

  • 1. Stargardt's pigmentosa: A novel combination of two inherited retinal dystrophies.
    Bartol-Puyal FA; Méndez-Martínez S; Pardiñas Barón N; Ruiz-Moreno Ó; Pablo L
    Arch Soc Esp Oftalmol (Engl Ed); 2023 Nov; 98(11):665-669. PubMed ID: 37748682
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.
    Klevering BJ; Maugeri A; Wagner A; Go SL; Vink C; Cremers FP; Hoyng CB
    Ophthalmology; 2004 Mar; 111(3):546-53. PubMed ID: 15019334
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Stargardt's disease and the ABCR gene.
    Westerfeld C; Mukai S
    Semin Ophthalmol; 2008; 23(1):59-65. PubMed ID: 18214793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inherited retinal dystrophies in a Kuwaiti tribe.
    Pandova MG; Abduljalil T; Elshafey AE; Abdelmoaty SMA; Albastawisy HI; Bastaki LA; Alsaleh H; Kozak I; AlMerjan JI
    Ophthalmic Genet; 2022 Aug; 43(4):438-445. PubMed ID: 35272565
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and genetic characteristics of late-onset Stargardt's disease.
    Westeneng-van Haaften SC; Boon CJ; Cremers FP; Hoefsloot LH; den Hollander AI; Hoyng CB
    Ophthalmology; 2012 Jun; 119(6):1199-210. PubMed ID: 22449572
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Outcome of ABCA4 disease-associated alleles in autosomal recessive retinal dystrophies: retrospective analysis in 420 Spanish families.
    Riveiro-Alvarez R; Lopez-Martinez MA; Zernant J; Aguirre-Lamban J; Cantalapiedra D; Avila-Fernandez A; Gimenez A; Lopez-Molina MI; Garcia-Sandoval B; Blanco-Kelly F; Corton M; Tatu S; Fernandez-San Jose P; Trujillo-Tiebas MJ; Ramos C; Allikmets R; Ayuso C
    Ophthalmology; 2013 Nov; 120(11):2332-7. PubMed ID: 23755871
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Experimental studies on medical treatments of retinal dystrophies with a particular focus on ABCA4 retinopathies.
    Sciezynska A; Ozieblo D; Oldak M
    Klin Oczna; 2016 Aug; 118(1):59-65. PubMed ID: 29715411
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mutations in the ABCA4 gene in a family with Stargardt's disease and retinitis pigmentosa (STGD1/RP19)].
    Rudolph G; Kalpadakis P; Haritoglou C; Rivera A; Weber BH
    Klin Monbl Augenheilkd; 2002 Aug; 219(8):590-6. PubMed ID: 12353176
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Inherited retinal diseases in patients with ABCA4 gene mutations].
    Sheremet NL; Grushke IG; Zhorzholadze NV; Tanas AS; Strelnikov VV
    Vestn Oftalmol; 2018; 134(4):68-73. PubMed ID: 30166513
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Biallelic
    Huckfeldt RM; Grigorian F; Place E; Comander JI; Vavvas D; Young LH; Yang P; Shurygina M; Pierce EA; Pennesi ME
    Mol Vis; 2020; 26():423-433. PubMed ID: 32565670
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis.
    Bini A; Sodi A; Passerini I; Menchini U; Torricelli F
    Clin Exp Ophthalmol; 2007 Nov; 35(8):777-9. PubMed ID: 17997789
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotypes Predispose Phenotypes-Clinical Features and Genetic Spectrum of
    Sung YC; Yang CH; Yang CM; Lin CW; Huang DS; Huang YS; Hu FR; Chen PL; Chen TC
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33261146
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cellular and Molecular Mechanisms of Pathogenesis Underlying Inherited Retinal Dystrophies.
    Manley A; Meshkat BI; Jablonski MM; Hollingsworth TJ
    Biomolecules; 2023 Feb; 13(2):. PubMed ID: 36830640
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration.
    Radu RA; Mata NL; Nusinowitz S; Liu X; Sieving PA; Travis GH
    Proc Natl Acad Sci U S A; 2003 Apr; 100(8):4742-7. PubMed ID: 12671074
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stargardt's disease and retinitis pigmentosa: different phenotypic presentations in the same family.
    Ozdek S; Onaran Z; Gürelik G; Bilgihan K; Acar C; Hasanreisoglu B
    Eye (Lond); 2005 Nov; 19(11):1222-5. PubMed ID: 15889047
    [No Abstract]   [Full Text] [Related]  

  • 16. Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy.
    Conley SM; Cai X; Makkia R; Wu Y; Sparrow JR; Naash MI
    Biochim Biophys Acta; 2012 Jul; 1822(7):1169-79. PubMed ID: 22033104
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A special form of Stargardt's disease/fundus flavimaculatus].
    Suzuki R; Hirose T
    Nippon Ganka Gakkai Zasshi; 1996 Jul; 100(7):562-7. PubMed ID: 8741342
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stargardt's disease: a review of the literature.
    Bither PP; Berns LA
    J Am Optom Assoc; 1988 Feb; 59(2):106-11. PubMed ID: 3283201
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.
    Klevering BJ; Deutman AF; Maugeri A; Cremers FP; Hoyng CB
    Graefes Arch Clin Exp Ophthalmol; 2005 Feb; 243(2):90-100. PubMed ID: 15614537
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa].
    Cremers FP; Maugeri A; Klevering BJ; Hoefsloot LH; Hoyng CB
    Ned Tijdschr Geneeskd; 2002 Aug; 146(34):1581-4. PubMed ID: 12224481
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.