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Journal Abstract Search

148 related items for PubMed ID: 5309737

  • 21. Golden tapetal-like fundus reflex and posterior hyaloid in a patient with x-linked juvenile retinoschisis.
    Miyake Y, Terasaki H.
    Retina; 1999; 19(1):84-6. PubMed ID: 10048383
    [No Abstract] [Full Text] [Related]

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  • 23. Diagnostic and therapeutic challenges.
    Genead MA, Fishman GA, Landeman M, Pennesi ME, Traboulsi EI.
    Retina; 2011 Feb; 31(2):413-8. PubMed ID: 20458258
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  • 25. Novel TULP1 mutation causing leber congenital amaurosis or early onset retinal degeneration.
    Mataftsi A, Schorderet DF, Chachoua L, Boussalah M, Nouri MT, Barthelmes D, Borruat FX, Munier FL.
    Invest Ophthalmol Vis Sci; 2007 Nov; 48(11):5160-7. PubMed ID: 17962469
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  • 26. Fluorescein angiography of hereditary retinal degenerations.
    Geltzer AI, Berson EL.
    Arch Ophthalmol; 1969 Jun; 81(6):776-82. PubMed ID: 4181959
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  • 27. Fluorescein photography of generalized dominant fundus dystrophy.
    Rosen ES, Leighton D.
    Br J Ophthalmol; 1968 Nov; 52(11):828-32. PubMed ID: 5696910
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  • 28. A new mutation in enhanced S-cone syndrome.
    Termühlen J, Alex AF, Glöckle N, Kellner U, Fiedler B, Eter N, Uhlig CE.
    Acta Ophthalmol; 2018 Jun; 96(4):e539-e540. PubMed ID: 27573156
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  • 33. [Fundus flavimaculatus].
    Kment H, Amalric P, Remky H.
    Klin Monbl Augenheilkd; 1967 Jun; 150(5):625-36. PubMed ID: 5586121
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  • 35. The Cohen syndrome. Retinal lesions and granulocytopenia.
    Warburg M, Pedersen SA, Hørlyk H.
    Ophthalmic Paediatr Genet; 1990 Mar; 11(1):7-13. PubMed ID: 2348983
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  • 40. The Wagner syndrome versus hereditary arthroophthalmopathy.
    Maumenee IH, Stoll HU, Mets MB.
    Trans Am Ophthalmol Soc; 1982 Mar; 80():349-65. PubMed ID: 7182967
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