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Journal Abstract Search

163 related items for PubMed ID: 3580827

  • 21. A case of Coats' disease in a low-birth-weight infant.
    Maruoka K, Yamamoto M, Fujita H, Tahara Y, Ishibashi T.
    Ophthalmologica; 2005; 219(6):401-3. PubMed ID: 16286803
    [Abstract] [Full Text] [Related]

  • 22. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child.
    Shields CL, Zahler J, Falk N, Furuta M, Eagle RC, Espinosa LE, Fischer PR, Shields JA.
    Arch Ophthalmol; 2007 Jun; 125(6):840-2. PubMed ID: 17563001
    [No Abstract] [Full Text] [Related]

  • 23. Idiopathic juxtafoveolar retinal telangiectasis. Update of classification and follow-up study.
    Gass JD, Blodi BA.
    Ophthalmology; 1993 Oct; 100(10):1536-46. PubMed ID: 8414413
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  • 24. Idiopathic juxtafoveolar retinal telangiectasis and pigment epithelial hyperplasia: an optical coherence tomographic study.
    Trabucchi G, Brancato R, Pierro L, Introini U, Sannace C.
    Arch Ophthalmol; 1999 Mar; 117(3):405-6. PubMed ID: 10088825
    [No Abstract] [Full Text] [Related]

  • 25. [Peripheral retinal telangiectasis in retinitis pigmentosa].
    Lodato G, Giuffre G, Anastasi M.
    J Fr Ophtalmol; 1987 Mar; 10(12):777-82. PubMed ID: 3450706
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  • 26. Focal parafoveal retinal telangiectasis.
    Hutton WL, Snyder WB, Fuller D, Vaiser A.
    Arch Ophthalmol; 1978 Aug; 96(8):1362-7. PubMed ID: 678172
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  • 28. [Coats' disease and familial retinal arteriolar tortuosity].
    Imai M, Iijima H.
    Nippon Ganka Gakkai Zasshi; 1990 Nov; 94(11):1091-6. PubMed ID: 2075874
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  • 32. Facioscapulohumeral dystrophy associated with mental retardation, hearing loss, and tortuosity of retinal arterioles.
    Matsuzaka T, Sakuragawa N, Terasawa K, Kuwabara H.
    J Child Neurol; 1986 Jul; 1(3):218-23. PubMed ID: 3598127
    [Abstract] [Full Text] [Related]

  • 33. Optical coherence tomography in group 2A idiopathic juxtafoveolar retinal telangiectasis.
    Gaudric A, Ducos de Lahitte G, Cohen SY, Massin P, Haouchine B.
    Arch Ophthalmol; 2006 Oct; 124(10):1410-9. PubMed ID: 17030708
    [Abstract] [Full Text] [Related]

  • 34. Group 2A idiopathic juxtafoveolar retinal telangiectasia in monozygotic twins.
    Siddiqui N, Fekrat S.
    Am J Ophthalmol; 2005 Mar; 139(3):568-70. PubMed ID: 15767084
    [Abstract] [Full Text] [Related]

  • 35. Ophthalmological findings in facioscapulohumeral dystrophy.
    Goselink RJM, Schreur V, van Kernebeek CR, Padberg GW, van der Maarel SM, van Engelen BGM, Erasmus CE, Theelen T.
    Brain Commun; 2019 Mar; 1(1):fcz023. PubMed ID: 32954265
    [Abstract] [Full Text] [Related]

  • 36. [A case of facioscapulohumeral muscular dystrophy with sensorineural hearing loss and retinal angioma].
    Fujimura H, Yoshikawa H, Ueno S, Yorifuji S, Tarui S.
    Rinsho Shinkeigaku; 1989 Nov; 29(11):1387-91. PubMed ID: 2625025
    [Abstract] [Full Text] [Related]

  • 37. Familial spastic paraplegia and maculopathy with juxtafoveolar retinal telangiectasis and subretinal neovascularization.
    Leys A, Gilbert HD, Van De Sompel W, Verougstraete C, Devriendt K, Lagae L, Gass JD.
    Retina; 2000 Nov; 20(2):184-9. PubMed ID: 10783952
    [Abstract] [Full Text] [Related]

  • 38. Facioscapulohumeral dystrophy: the role of inflammation.
    Fitzsimons RB.
    Lancet; 1994 Oct 01; 344(8927):902-3. PubMed ID: 7934342
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  • 40. Idiopathic juxtafoveal retinal telangiectasia.
    Wu J, Ferrucci S.
    Optometry; 2008 Nov 01; 79(11):653-62. PubMed ID: 19811762
    [Abstract] [Full Text] [Related]

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