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Journal Abstract Search

131 related items for PubMed ID: 3428076

  • 21. Electrophysiological findings in familial exudative vitreoretinopathy.
    Ohkubo H, Tanino T.
    Doc Ophthalmol; 1987 Apr; 65(4):461-9. PubMed ID: 3691294
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  • 29. [Goldmann-Favre syndrome--case report].
    Brydak-Godowska J, Makowiec-Tabernacka M.
    Klin Oczna; 2009 Apr; 111(10-12):346-7. PubMed ID: 20169893
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  • 31. Electroretinography and electro-oculography to localize abnormalities in early-stage inflammatory eye disease.
    Ikeda H, Franchi A, Turner G, Shilling J, Graham E.
    Doc Ophthalmol; 1989 Dec; 73(4):387-94. PubMed ID: 2637121
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  • 34. Identification of XLRS1 gene mutation (608C > T) in a Portuguese family with juvenile retinoschisis.
    Teixeira C, Rocha-Sousa A, Trump D, Brandão E, Falcão-Reis F.
    Eur J Ophthalmol; 2005 Dec; 15(5):638-40. PubMed ID: 16167295
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  • 37. WAGNER syndrome: anatomic, functional and genetic characterization of a Portuguese family.
    Araújo JR, Tavares-Ferreira J, Estrela-Silva S, Rocha P, Brandão E, Faria PA, Falcão-Reis F, Rocha-Sousa A.
    Graefes Arch Clin Exp Ophthalmol; 2018 Jan; 256(1):163-171. PubMed ID: 29071374
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  • 39. Elevated macular retinoschisis associated with Goldmann-Favre syndrome successfully treated with grid laser photocoagulation.
    Khairallah M, Ladjimi A, Ben Yahia S, Zaouali S, Messaoud R, Boulima K.
    Retina; 2002 Apr; 22(2):234-7. PubMed ID: 11927864
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  • 40. Histopathological findings of X-linked retinoschisis with neovascular glaucoma.
    Ando A, Takahashi K, Sho K, Matsushima M, Okamura A, Uyama M.
    Graefes Arch Clin Exp Ophthalmol; 2000 Jan; 238(1):1-7. PubMed ID: 10664045
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