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Journal Abstract Search

287 related items for PubMed ID: 8190471

  • 1. Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.
    Sigesmund DA, Weleber RG, Pillers DA, Westall CA, Panton CM, Powell BR, Héon E, Murphey WH, Musarella MA, Ray PN.
    Ophthalmology; 1994 May; 101(5):856-65. PubMed ID: 8190471
    [Abstract] [Full Text] [Related]

  • 2. Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system.
    Ricotti V, Jägle H, Theodorou M, Moore AT, Muntoni F, Thompson DA.
    Eur J Hum Genet; 2016 Apr; 24(4):562-8. PubMed ID: 26081639
    [Abstract] [Full Text] [Related]

  • 3. Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.
    Pillers DA, Weleber RG, Green DG, Rash SM, Dally GY, Howard PL, Powers MR, Hood DC, Chapman VM, Ray PN, Woodward WR.
    Mol Genet Metab; 1999 Feb; 66(2):100-10. PubMed ID: 10068512
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  • 4. [Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy].
    Yang Y, Zhang C, Sheng W, Pan S, Wu D, Jiang F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):32-4. PubMed ID: 11172639
    [Abstract] [Full Text] [Related]

  • 5. mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy.
    Pillers DA, Weleber RG, Woodward WR, Green DG, Chapman VM, Ray PN.
    Invest Ophthalmol Vis Sci; 1995 Feb; 36(2):462-6. PubMed ID: 7843915
    [Abstract] [Full Text] [Related]

  • 6. Asymmetrical Functional Deficits of ON and OFF Retinal Processing in the mdx3Cv Mouse Model of Duchenne Muscular Dystrophy.
    Tsai TI, Barboni MT, Nagy BV, Roux MJ, Rendon A, Ventura DF, Kremers J.
    Invest Ophthalmol Vis Sci; 2016 Oct 01; 57(13):5788-5798. PubMed ID: 27792813
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  • 7. Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations.
    Pillers DA, Fitzgerald KM, Duncan NM, Rash SM, White RA, Dwinnell SJ, Powell BR, Schnur RE, Ray PN, Cibis GW, Weleber RG.
    Hum Genet; 1999 Oct 01; 105(1-2):2-9. PubMed ID: 10480348
    [Abstract] [Full Text] [Related]

  • 8. The effects of dystrophin gene mutations on the ERG in mice and humans.
    Cibis GW, Fitzgerald KM, Harris DJ, Rothberg PG, Rupani M.
    Invest Ophthalmol Vis Sci; 1993 Dec 01; 34(13):3646-52. PubMed ID: 8258524
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  • 9. Electroretinogram in Duchenne/Becker muscular dystrophy.
    Pascual Pascual SI, Molano J, Pascual-Castroviejo I.
    Pediatr Neurol; 1998 Apr 01; 18(4):315-20. PubMed ID: 9588526
    [Abstract] [Full Text] [Related]

  • 10. Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway.
    Fitzgerald KM, Cibis GW, Giambrone SA, Harris DJ.
    J Clin Invest; 1994 Jun 01; 93(6):2425-30. PubMed ID: 8200977
    [Abstract] [Full Text] [Related]

  • 11. Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.
    Jensen H, Warburg M, Sjö O, Schwartz M.
    J Med Genet; 1995 May 01; 32(5):348-51. PubMed ID: 7616540
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  • 13. Dystrophin expression in the human retina is required for normal function as defined by electroretinography.
    Pillers DA, Bulman DE, Weleber RG, Sigesmund DA, Musarella MA, Powell BR, Murphey WH, Westall C, Panton C, Becker LE.
    Nat Genet; 1993 May 01; 4(1):82-6. PubMed ID: 8513332
    [Abstract] [Full Text] [Related]

  • 14. ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy.
    Fitzgerald KM, Cibis GW, Gettel AH, Rinaldi R, Harris DJ, White RA.
    J Med Genet; 1999 Apr 01; 36(4):316-22. PubMed ID: 10227401
    [Abstract] [Full Text] [Related]

  • 15. Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram but not congenital stationary night blindness.
    Tremblay F, De Becker I, Dooley JM, Riddell DC.
    Can J Ophthalmol; 1994 Dec 01; 29(6):274-9. PubMed ID: 7834566
    [Abstract] [Full Text] [Related]

  • 16. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.
    Ophthalmology; 2002 Oct 01; 109(10):1862-70. PubMed ID: 12359607
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  • 18. Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram and normal dark adaptation.
    Tremblay F, De Becker I, Riddell DC, Dooley JM.
    Can J Ophthalmol; 1994 Dec 01; 29(6):280-3. PubMed ID: 7834567
    [Abstract] [Full Text] [Related]

  • 19. Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy.
    Barboni MTS, Liber AMP, Joachimsthaler A, Saoudi A, Goyenvalle A, Rendon A, Roger JE, Ventura DF, Kremers J, Vaillend C.
    Neurobiol Dis; 2021 May 01; 152():105288. PubMed ID: 33556541
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