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Journal Abstract Search

288 related items for PubMed ID: 10786061

  • 21. [Evidence-based diagnostic approach to inherited retinal dystrophies 2009].
    Kellner U, Kellner S, Renner AB, Fiebig BS, Weinitz S, Weber BH.
    Klin Monbl Augenheilkd; 2009 Dec; 226(12):999-1011. PubMed ID: 19757352
    [Abstract] [Full Text] [Related]

  • 22. Fundus autofluorescence imaging in Best's vitelliform dystrophy.
    Jarc-Vidmar M, Kraut A, Hawlina M.
    Klin Monbl Augenheilkd; 2003 Dec; 220(12):861-7. PubMed ID: 14704944
    [Abstract] [Full Text] [Related]

  • 23. [Normal fundus and abnormal electroretinogram: differential diagnosis].
    Niemeyer G, Schaefer A.
    Klin Monbl Augenheilkd; 2002 Apr; 219(4):259-63. PubMed ID: 12022013
    [Abstract] [Full Text] [Related]

  • 24. [Macular and multifocal electroretinography in the diagnosis of Stargardt's dystrophy].
    Zol'nikova IV, Karlova IZ, Rogatina EV.
    Vestn Oftalmol; 2009 Apr; 125(1):41-6. PubMed ID: 19284101
    [Abstract] [Full Text] [Related]

  • 25. [Localized forms of retinopathia pigmentosa].
    Lessel MR, Thaler AR, Heilig P.
    Wien Klin Wochenschr; 1986 May 02; 98(9):264-9. PubMed ID: 3727597
    [Abstract] [Full Text] [Related]

  • 26. [Flash full-field electroretinography in diseases with night blindness].
    Pojda-Wilczek D, Herba E, Pojda SM.
    Klin Oczna; 2005 May 02; 107(1-3):28-30. PubMed ID: 16052794
    [Abstract] [Full Text] [Related]

  • 27. Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic study.
    Burstedt MS, Ristoff E, Larsson A, Wachtmeister L.
    Ophthalmology; 2009 Feb 02; 116(2):324-31. PubMed ID: 19111905
    [Abstract] [Full Text] [Related]

  • 28. A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene.
    Nakamura M, Hotta Y, Tanikawa A, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2000 Nov 02; 41(12):3925-32. PubMed ID: 11053295
    [Abstract] [Full Text] [Related]

  • 29. Use of the ERG and EOG in evaluating the effect of sleep deprivation on visual function in flying personnel.
    Tasker DI, Kinel SG, Tredici TJ.
    Aviat Space Environ Med; 1975 Jul 02; 46(7):943-5. PubMed ID: 1156304
    [Abstract] [Full Text] [Related]

  • 30. Leber's congenital tapetoretinal degeneration.
    Francois J.
    Int Ophthalmol Clin; 1968 Jul 02; 8(4):929-47. PubMed ID: 5741529
    [No Abstract] [Full Text] [Related]

  • 31. Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.
    Mantel I, Brantley MA, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT.
    Klin Monbl Augenheilkd; 2004 May 02; 221(5):427-30. PubMed ID: 15162299
    [Abstract] [Full Text] [Related]

  • 32. Characteristic ERG-flicker anomaly in incomplete congenital stationary night blindness.
    Miyake Y, Horiguchi M, Ota I, Shiroyama N.
    Invest Ophthalmol Vis Sci; 1987 Nov 02; 28(11):1816-23. PubMed ID: 3499417
    [Abstract] [Full Text] [Related]

  • 33. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
    Renner AB, Kellner U, Cropp E, Preising MN, MacDonald IM, van den Hurk JA, Cremers FP, Foerster MH.
    Ophthalmology; 2006 Nov 02; 113(11):2066.e1-10. PubMed ID: 16935340
    [Abstract] [Full Text] [Related]

  • 34. Metabolic and functional changes in retinitis pigmentosa: comparing retinal vessel oximetry to full-field electroretinography, electrooculogram and multifocal electroretinography.
    Todorova MG, Türksever C, Schötzau A, Schorderet DF, Valmaggia C.
    Acta Ophthalmol; 2016 May 02; 94(3):e231-41. PubMed ID: 26490228
    [Abstract] [Full Text] [Related]

  • 35. [Epidemiology and prevalence of hereditary retinal dystrophies in the Northern France].
    Puech B, Kostrubiec B, Hache JC, François P.
    J Fr Ophtalmol; 1991 May 02; 14(3):153-64. PubMed ID: 1918822
    [Abstract] [Full Text] [Related]

  • 36. Retinal degeneration in retinitis pigmentosa and neuronal ceroid lipofuscinosis: An overview.
    Birch DG.
    Mol Genet Metab; 1999 Apr 02; 66(4):356-66. PubMed ID: 10191129
    [Abstract] [Full Text] [Related]

  • 37. The C-wave in hereditary degenerations of the ocular fundus.
    Röver J, Bach M.
    Doc Ophthalmol; 1985 Aug 30; 60(2):127-32. PubMed ID: 4042819
    [Abstract] [Full Text] [Related]

  • 38. The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.
    Schuster A, Janecke AR, Wilke R, Schmid E, Thompson DA, Utermann G, Wissinger B, Zrenner E, Gal A.
    Invest Ophthalmol Vis Sci; 2007 Apr 30; 48(4):1824-31. PubMed ID: 17389517
    [Abstract] [Full Text] [Related]

  • 39. Fundus albipunctatus and other flecked retina syndromes.
    Flynn MF, Bohnert D.
    J Am Optom Assoc; 1999 Sep 30; 70(9):571-80. PubMed ID: 10547972
    [Abstract] [Full Text] [Related]

  • 40. Local ERG for clinical examination of eye diseases.
    Shamshinova AM.
    Doc Ophthalmol; 1990 Nov 30; 76(1):1-11. PubMed ID: 2078979
    [Abstract] [Full Text] [Related]

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