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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 7257747

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  • 2. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy].
    Vallat M, Fritsch D, Van Coppenolle F, Detre J, Moze M, Rabourdin F.
    J Fr Ophtalmol; 1985; 8(4):301-7. PubMed ID: 4020040
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  • 7. [A case of heriditary arthro-ophthalmopathy: Stickler's syndrome].
    Brihaye-Van Geertruyden M, Verlaeken L, Herzeel R, Swinnen MC, Malfroot A.
    Bull Soc Belge Ophtalmol; 1979; 183():143-7. PubMed ID: 526682
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  • 11. Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous.
    Arikawa A, Yoshida S, Yoshikawa H, Ishikawa K, Yamaji Y, Arita RI, Ueno A, Ishibashi T.
    Eye (Lond); 2010 Feb; 24(2):391-3. PubMed ID: 19461663
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  • 12. The pseudo-posterior limiting layer syndrome: a vitreoretinal heredodegeneration with autosomal dominant transmission.
    Rossier J, Eisner G.
    Graefes Arch Clin Exp Ophthalmol; 1994 Jan; 232(1):16-24. PubMed ID: 8119597
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  • 14. Lattice degeneration in a family: with retinal detachment and cataract.
    Lewkonia I, Davies MS, Salmon JD.
    Br J Ophthalmol; 1973 Aug; 57(8):566-71. PubMed ID: 4743918
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  • 15. A case of erosive vitreoretinopathy.
    Kyung SE, Chang MH, Ji JY.
    Korean J Ophthalmol; 2002 Jun; 16(1):47-51. PubMed ID: 12162518
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  • 18. Wagner's vitreoretinal degeneration with generalized epiphyseal dysplasia.
    Godel V, Lazar M.
    Acta Ophthalmol (Copenh); 1982 Jun; 60(3):469-74. PubMed ID: 7136558
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