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Journal Abstract Search

194 related items for PubMed ID: 7616540

  • 1. 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; 32(5):348-51. PubMed ID: 7616540
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  • 2. 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; 29(6):274-9. PubMed ID: 7834566
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  • 5. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.
    Bech-Hansen NT, Boycott KM, Gratton KJ, Ross DA, Field LL, Pearce WG.
    Hum Genet; 1998 Aug; 103(2):124-30. PubMed ID: 9760193
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  • 7. 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
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  • 8. A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness.
    Mahmood U, Méjécase C, Ali SMA, Moosajee M, Kozak I.
    Genes (Basel); 2021 Jan 27; 12(2):. PubMed ID: 33513752
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  • 9. Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.
    Pillers DA, Towbin JA, Chamberlain JS, Wu D, Ranier J, Powell BR, McCabe ER.
    Am J Hum Genet; 1990 Nov 27; 47(5):795-801. PubMed ID: 2220819
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  • 11. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.
    Ruether K, Apfelstedt-Sylla E, Zrenner E.
    Ger J Ophthalmol; 1993 Nov 27; 2(6):429-35. PubMed ID: 8312830
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  • 12. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
    Boycott KM, Pearce WG, Bech-Hansen NT.
    Can J Ophthalmol; 2000 Jun 27; 35(4):204-13. PubMed ID: 10900517
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  • 13. 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 27; 34(13):3646-52. PubMed ID: 8258524
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  • 15. Congenital stationary night blindness.
    Haim M.
    Acta Ophthalmol (Copenh); 1986 Apr 27; 64(2):192-8. PubMed ID: 3487908
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  • 16. Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.
    Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E.
    Vision Res; 2002 May 27; 42(11):1475-83. PubMed ID: 12044753
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  • 19. 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 27; 36(4):316-22. PubMed ID: 10227401
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