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Journal Abstract Search

181 related items for PubMed ID: 1495763

  • 1. Peters' anomaly and combination with other malformations (series of 16 patients).
    Mayer UM.
    Ophthalmic Paediatr Genet; 1992 Jun; 13(2):131-5. PubMed ID: 1495763
    [Abstract] [Full Text] [Related]

  • 2. Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins.
    Cronemberger S, Albuquerque ALB, Silva ACSE, Zanini JLSS, da Silva AHG, Barbosa LF, da Cunha Rubião F, de Lima FL, Casimiro RF, Martins MP, Diniz-Filho A, Bastos-Rodrigues L, Friedman E, De Marco L.
    Acta Paediatr; 2024 Jun; 113(6):1420-1425. PubMed ID: 38363039
    [Abstract] [Full Text] [Related]

  • 3. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
    Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, Halimi P, Roche O, Van Regemorter N, Munier F, Schorderet D, Dufier JL, Marsac C, Ricquier D, Menasche M, Penfornis A, Abitbol M.
    Mol Vis; 2007 Apr 02; 13():511-23. PubMed ID: 17417613
    [Abstract] [Full Text] [Related]

  • 4. Peters' anomaly. The spectrum of associated ocular and systemic malformations.
    Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA.
    Ophthalmic Paediatr Genet; 1992 Jun 02; 13(2):137-43. PubMed ID: 1495764
    [Abstract] [Full Text] [Related]

  • 5. Optimising keratoplasty for Peters' anomaly in infants using spectral-domain optical coherence tomography.
    Hong J, Yang Y, Cursiefen C, Mashaghi A, Wu D, Liu Z, Sun X, Dana R, Xu J.
    Br J Ophthalmol; 2017 Jun 02; 101(6):820-827. PubMed ID: 27660330
    [Abstract] [Full Text] [Related]

  • 6. Corneal coloboma, aphakia and retinal neovascularization with anterior segment dysgenesis (Peters' anomaly).
    Gunderson CA, Stone R, Peiffer R, Freedman S.
    Ophthalmologica; 1996 Jun 02; 210(6):361-6. PubMed ID: 8887396
    [Abstract] [Full Text] [Related]

  • 7. Peters anomaly in PHACE syndrome.
    Shabeeb NM, Plager DA, Haggstrom AN.
    J AAPOS; 2017 Aug 02; 21(4):331-333. PubMed ID: 28713056
    [Abstract] [Full Text] [Related]

  • 8. Foxe3 haploinsufficiency in mice: a model for Peters' anomaly.
    Ormestad M, Blixt A, Churchill A, Martinsson T, Enerbäck S, Carlsson P.
    Invest Ophthalmol Vis Sci; 2002 May 02; 43(5):1350-7. PubMed ID: 11980846
    [Abstract] [Full Text] [Related]

  • 9. Long-term clinical course and visual outcome associated with Peters' anomaly.
    Chang JW, Kim JH, Kim SJ, Yu YS.
    Eye (Lond); 2012 Sep 02; 26(9):1237-42. PubMed ID: 22744393
    [Abstract] [Full Text] [Related]

  • 10. Unilateral Peters' anomaly complicated by a corneal tattoo.
    Pomella KM, Wagner H.
    Optom Vis Sci; 1998 Sep 02; 75(9):635-9. PubMed ID: 9778695
    [Abstract] [Full Text] [Related]

  • 11. Vitreoretinal dysplasia masquerading as Peters' anomaly.
    Martinet V, Dureau P, Bergès O, Caputo G.
    Eur J Ophthalmol; 2010 Sep 02; 20(1):228-30. PubMed ID: 19882524
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  • 16. PAX 6 is normal in most cases of Peters' anomaly.
    Churchill AJ, Booth AP, Anwar R, Markham AF.
    Eye (Lond); 1998 Sep 02; 12 ( Pt 2)():299-303. PubMed ID: 9683959
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  • 18. Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly.
    Hanson IM, Fletcher JM, Jordan T, Brown A, Taylor D, Adams RJ, Punnett HH, van Heyningen V.
    Nat Genet; 1994 Feb 02; 6(2):168-73. PubMed ID: 8162071
    [Abstract] [Full Text] [Related]

  • 19. A case of atypical WAGR syndrome with anterior segment anomaly and microphthalmos.
    Kawase E, Tanaka K, Honna T, Azuma N.
    Arch Ophthalmol; 2001 Dec 02; 119(12):1855-6. PubMed ID: 11735802
    [No Abstract] [Full Text] [Related]

  • 20. A donor twin discordant with Peters anomaly in a twin-twin transfusion syndrome case: a case report.
    Chang YL, Chao AS, Chou CY, Chang SD, Chiang MC, Lee YS.
    BMC Pregnancy Childbirth; 2020 Sep 23; 20(1):558. PubMed ID: 32967640
    [Abstract] [Full Text] [Related]

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