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472 related items for PubMed ID: 27485810

  • 1. Bull's eye and pigment maculopathy are further retinal manifestations of an abnormal Bruch's membrane in Alport syndrome.
    Savige J, Wang Y, Crawford A, Smith J, Symons A, Mack H, Nicholls K, Wilson D, Colville D.
    Ophthalmic Genet; 2017; 38(3):238-244. PubMed ID: 27485810
    [Abstract] [Full Text] [Related]

  • 2. Retinal basement membrane abnormalities and the retinopathy of Alport syndrome.
    Savige J, Liu J, DeBuc DC, Handa JT, Hageman GS, Wang YY, Parkin JD, Vote B, Fassett R, Sarks S, Colville D.
    Invest Ophthalmol Vis Sci; 2010 Mar; 51(3):1621-7. PubMed ID: 19850830
    [Abstract] [Full Text] [Related]

  • 3. Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
    Chen Y, Colville D, Ierino F, Symons A, Savige J.
    Ophthalmic Genet; 2018 Apr; 39(2):208-214. PubMed ID: 29172845
    [Abstract] [Full Text] [Related]

  • 4. Ocular features in Alport syndrome: pathogenesis and clinical significance.
    Savige J, Sheth S, Leys A, Nicholson A, Mack HG, Colville D.
    Clin J Am Soc Nephrol; 2015 Apr 07; 10(4):703-9. PubMed ID: 25649157
    [Abstract] [Full Text] [Related]

  • 5. Bull'S eye maculopathy in a patient taking sertraline.
    Mason JO, Patel SA.
    Retin Cases Brief Rep; 2015 Apr 07; 9(2):131-3. PubMed ID: 25401995
    [Abstract] [Full Text] [Related]

  • 6. Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
    Shaw EA, Colville D, Wang YY, Zhang KW, Dagher H, Fassett R, Guymer R, Savige J.
    Nephrol Dial Transplant; 2007 Jan 07; 22(1):104-8. PubMed ID: 17071739
    [Abstract] [Full Text] [Related]

  • 7. En face optical coherence tomography findings in a case of Alport syndrome.
    Cho IH, Kim HD, Jung SJ, Park TK.
    Indian J Ophthalmol; 2017 Sep 07; 65(9):877-879. PubMed ID: 28905837
    [Abstract] [Full Text] [Related]

  • 8. [A new case of giant macular hole in a patient with Alport syndrome].
    Mercé E, Korobelnik JF, Delyfer MN, Rougier MB.
    J Fr Ophtalmol; 2012 Oct 07; 35(8):573-9. PubMed ID: 22695059
    [Abstract] [Full Text] [Related]

  • 9. Retinal findings in patients with Alport Syndrome: expanding the clinical spectrum.
    Fawzi AA, Lee NG, Eliott D, Song J, Stewart JM.
    Br J Ophthalmol; 2009 Dec 07; 93(12):1606-11. PubMed ID: 19635720
    [Abstract] [Full Text] [Related]

  • 10. BULL'S EYE MACULOPATHY WITH MUTATIONS IN RDS/PRPH2 AND ROM-1.
    Essilfie JO, Sanfilippo CJ, Sarraf D.
    Retin Cases Brief Rep; 2009 Dec 07; 12 Suppl 1():S55-S58. PubMed ID: 29155698
    [Abstract] [Full Text] [Related]

  • 11. Retinal dystrophies with bull's-eye maculopathy along with negative ERGs.
    Nasser F, Kurtenbach A, Kohl S, Obermaier C, Stingl K, Zrenner E.
    Doc Ophthalmol; 2019 Aug 07; 139(1):45-57. PubMed ID: 30945053
    [Abstract] [Full Text] [Related]

  • 12. The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failure.
    Colville D, Wang YY, Tan R, Savige J.
    Br J Ophthalmol; 2009 Mar 07; 93(3):383-6. PubMed ID: 19019929
    [Abstract] [Full Text] [Related]

  • 13. Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy.
    Seddon JM, Afshari MA, Sharma S, Bernstein PS, Chong S, Hutchinson A, Petrukhin K, Allikmets R.
    Ophthalmology; 2001 Nov 07; 108(11):2060-7. PubMed ID: 11713080
    [Abstract] [Full Text] [Related]

  • 14. Autologous transplantation of retinal pigment epithelium-Bruch's membrane complex for hemorrhagic age-related macular degeneration.
    Ma Z, Han L, Wang C, Dou H, Hu Y, Feng X, Xu Y, Wang Z, Yin Z, Liu Y.
    Invest Ophthalmol Vis Sci; 2009 Jun 07; 50(6):2975-81. PubMed ID: 19117919
    [Abstract] [Full Text] [Related]

  • 15. Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull's Eye Maculopathy.
    Collison FT, Xie YA, Gambin T, Jhangiani S, Muzny D, Gibbs R, Lupski JR, Fishman GA, Allikmets R.
    Ophthalmic Genet; 2015 Jun 07; 36(3):270-5. PubMed ID: 25687216
    [Abstract] [Full Text] [Related]

  • 16. Frail inner limiting membrane maculopathy suggested to describe a new retinal Alport-like condition with two variants in three generations of females.
    Petersen SD, Belmouhand M, Hertz JM, Fagerberg C, Brasch-Andersen C, Grauslund J, Munier FL, Larsen M.
    Ophthalmic Genet; 2024 Jun 07; 45(3):281-288. PubMed ID: 38197426
    [Abstract] [Full Text] [Related]

  • 17. Bilateral giant macular holes: A rare manifestation of Alport syndrome.
    Raimundo M, Fonseca C, Silva R, Figueira J.
    Eur J Ophthalmol; 2019 Jan 07; 29(1):NP13-NP16. PubMed ID: 29873249
    [Abstract] [Full Text] [Related]

  • 18. G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull's eye maculopathy.
    Cella W, Greenstein VC, Zernant-Rajang J, Smith TR, Barile G, Allikmets R, Tsang SH.
    Exp Eye Res; 2009 Jun 15; 89(1):16-24. PubMed ID: 19217903
    [Abstract] [Full Text] [Related]

  • 19. [Rare ocular manifestation with suspect alport syndrome].
    Krejčířová I, Varadyová B, Doležel Z, Autrata R, Matúšová J, Gregorová E.
    Cesk Slov Oftalmol; 2014 Jun 15; 70(3):114-8. PubMed ID: 25032798
    [Abstract] [Full Text] [Related]

  • 20. Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19).
    Mizobuchi K, Hayashi T, Ohira R, Nakano T.
    Doc Ophthalmol; 2023 Jun 15; 146(3):281-291. PubMed ID: 37162688
    [Abstract] [Full Text] [Related]

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