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Journal Abstract Search


107 related items for PubMed ID: 11729740

  • 1. [Multifocal ERG in central areolar choroidal dystrophy].
    Feigl B, Haas A.
    Ophthalmologe; 2001 Nov; 98(11):1074-8. PubMed ID: 11729740
    [Abstract] [Full Text] [Related]

  • 2. Full-field electroretinograms in patients with central areolar choroidal dystrophy.
    Ponjavic V, Andréasson S, Ehinger B.
    Acta Ophthalmol (Copenh); 1994 Oct; 72(5):537-44. PubMed ID: 7887150
    [Abstract] [Full Text] [Related]

  • 3. Use of the multifocal electroretinogram in the evaluation of a patient with central areolar choroidal dystrophy.
    Hartley KL, Blodi BA, VerHoeve JN.
    Am J Ophthalmol; 2002 Jun; 133(6):852-4. PubMed ID: 12036692
    [Abstract] [Full Text] [Related]

  • 4. Early findings in central areolar choroidal dystrophy.
    Hoyng CB, Pinckers AJ, Deutman AF.
    Acta Ophthalmol (Copenh); 1990 Jun; 68(3):356-60. PubMed ID: 2392919
    [Abstract] [Full Text] [Related]

  • 5. The development of central areolar choroidal dystrophy.
    Hoyng CB, Deutman AF.
    Graefes Arch Clin Exp Ophthalmol; 1996 Feb; 234(2):87-93. PubMed ID: 8720677
    [Abstract] [Full Text] [Related]

  • 6. Detection of retinal dysfunction in vitelliform macular dystrophy using the multifocal ERG (MF-ERG).
    Palmowski AM, Allgayer R, Heinemann-Vernaleken B, Scherer V, Ruprecht KW.
    Doc Ophthalmol; 2003 Mar; 106(2):145-52. PubMed ID: 12678279
    [Abstract] [Full Text] [Related]

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  • 8. Electroretinograms and pattern visually evoked cortical potentials in central areolar choroidal dystrophy.
    Adachi-Usami E, Murayama K, Yamamoto Y.
    Doc Ophthalmol; 1990 Aug; 75(1):33-40. PubMed ID: 2265574
    [Abstract] [Full Text] [Related]

  • 9. Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction.
    Jonasson F, Sander B, Eysteinsson T, Jörgensen T, Klintworth GK.
    Acta Ophthalmol Scand; 2007 Dec; 85(8):862-7. PubMed ID: 17683515
    [Abstract] [Full Text] [Related]

  • 10. Electrophysiology findings in a large family with central areolar choroidal dystrophy.
    Lotery AJ, Silvestri G, Collins AD.
    Doc Ophthalmol; 2007 Dec; 97(2):103-19. PubMed ID: 10765965
    [Abstract] [Full Text] [Related]

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  • 13. Electrophysiological assessment for early detection of retinal dysfunction in β-thalassemia major patients.
    Dettoraki M, Kattamis A, Ladas I, Maragkos K, Koutsandrea C, Chatzistefanou K, Laios K, Brouzas D, Moschos MM.
    Graefes Arch Clin Exp Ophthalmol; 2017 Jul; 255(7):1349-1358. PubMed ID: 28361176
    [Abstract] [Full Text] [Related]

  • 14. [A new approach for studying the retinal and choroidal circulation].
    Yoneya S.
    Nippon Ganka Gakkai Zasshi; 2004 Dec; 108(12):836-61; discussion 862. PubMed ID: 15656089
    [Abstract] [Full Text] [Related]

  • 15. [The value of multifocal ERG in diagnosis of discrete macular dystrophies].
    Zaninetti M, Safran AB.
    Klin Monbl Augenheilkd; 2004 May; 221(5):379-82. PubMed ID: 15162285
    [Abstract] [Full Text] [Related]

  • 16. [Macular and multifocal electroretinography in the evaluation of the retinal macular region function in age-related macular degeneration].
    Zol'nikova IV, Karlova IZ, Ponomareva EN, Viadro EV, Zhamshinova AM.
    Vestn Oftalmol; 2009 May; 125(1):27-32. PubMed ID: 19284097
    [Abstract] [Full Text] [Related]

  • 17. Autosomal dominant occult macular dystrophy with an RP1L1 mutation (R45W).
    Hayashi T, Gekka T, Kozaki K, Ohkuma Y, Tanaka I, Yamada H, Tsuneoka H.
    Optom Vis Sci; 2012 May; 89(5):684-91. PubMed ID: 22504327
    [Abstract] [Full Text] [Related]

  • 18. 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; 109(10):1862-70. PubMed ID: 12359607
    [Abstract] [Full Text] [Related]

  • 19. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
    [Abstract] [Full Text] [Related]

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