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Journal Abstract Search

907 related items for PubMed ID: 16650681

  • 1. Hypotrichosis with juvenile macular dystrophy: clinical and electrophysiological assessment of visual function.
    Leibu R, Jermans A, Hatim G, Miller B, Sprecher E, Perlman I.
    Ophthalmology; 2006 May; 113(5):841-7.e3. PubMed ID: 16650681
    [Abstract] [Full Text] [Related]

  • 2. Long-term follow-up of Stargardt's disease and fundus flavimaculatus.
    Armstrong JD, Meyer D, Xu S, Elfervig JL.
    Ophthalmology; 1998 Mar; 105(3):448-57; discussion 457-8. PubMed ID: 9499775
    [Abstract] [Full Text] [Related]

  • 3. Alström syndrome--a case report and literature review.
    Karska-Basta I, Kubicka-Trzaska A, Filemonowicz-Skoczek A, Romanowska-Dixon B, Kobylarz J.
    Klin Oczna; 2008 Mar; 110(4-6):188-92. PubMed ID: 18655459
    [Abstract] [Full Text] [Related]

  • 4. Retinal pigment epithelial dysfunction in human immunodeficiency virus-infected patients with cytomegalovirus retinitis.
    Harrison JM, van Heuven WA.
    Ophthalmology; 1999 Apr; 106(4):790-7. PubMed ID: 10201604
    [Abstract] [Full Text] [Related]

  • 5. Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.
    Booij JC, Boon CJ, van Schooneveld MJ, ten Brink JB, Bakker A, de Jong PT, Hoyng CB, Bergen AA, Klaver CC.
    Ophthalmology; 2010 Jul; 117(7):1415-22. PubMed ID: 20381869
    [Abstract] [Full Text] [Related]

  • 6. Multifocal electroretinogram in occult macular dystrophy.
    Piao CH, Kondo M, Tanikawa A, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2000 Feb; 41(2):513-7. PubMed ID: 10670483
    [Abstract] [Full Text] [Related]

  • 7. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy.
    Birch DG, Anderson JL, Fish GE.
    Ophthalmology; 1999 Feb; 106(2):258-68. PubMed ID: 9951474
    [Abstract] [Full Text] [Related]

  • 8. Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.
    Hull S, Arno G, Robson AG, Broadgate S, Plagnol V, McKibbin M, Halford S, Michaelides M, Holder GE, Moore AT, Khan KN, Webster AR.
    JAMA Ophthalmol; 2016 Sep 01; 134(9):992-1000. PubMed ID: 27386845
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 116(2):324-31. PubMed ID: 19111905
    [Abstract] [Full Text] [Related]

  • 10. Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus.
    Lois N, Holder GE, Fitzke FW, Plant C, Bird AC.
    Invest Ophthalmol Vis Sci; 1999 Oct 01; 40(11):2668-75. PubMed ID: 10509664
    [Abstract] [Full Text] [Related]

  • 11. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun 01; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 12. Cone dystrophies: clinical and electrophysiological findings.
    Kellner U, Kleine-Hartlage P, Foerster MH.
    Ger J Ophthalmol; 1992 Jun 01; 1(2):105-9. PubMed ID: 1477624
    [Abstract] [Full Text] [Related]

  • 13. Late onset is common in best macular dystrophy associated with VMD2 gene mutations.
    Renner AB, Tillack H, Kraus H, Krämer F, Mohr N, Weber BH, Foerster MH, Kellner U.
    Ophthalmology; 2005 Apr 01; 112(4):586-92. PubMed ID: 15808248
    [Abstract] [Full Text] [Related]

  • 14. Electroretinographic monitoring in birdshot chorioretinopathy.
    Sobrin L, Lam BL, Liu M, Feuer WJ, Davis JL.
    Am J Ophthalmol; 2005 Jul 01; 140(1):52-64. PubMed ID: 16038651
    [Abstract] [Full Text] [Related]

  • 15. [Electroretinogram and electrooculogram in a family with Stargardt's disease].
    Pojda-Wilczek D, Makowiecka-Obidzińska K, Herba E.
    Klin Oczna; 2004 Jul 01; 106(3 Suppl):540-1. PubMed ID: 15636262
    [Abstract] [Full Text] [Related]

  • 16. "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
    Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, Hunt DM, Moore AT, Holder GE.
    Retina; 2010 Jan 01; 30(1):51-62. PubMed ID: 19952985
    [Abstract] [Full Text] [Related]

  • 17. Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings.
    Indelman M, Leibu R, Jammal A, Bergman R, Sprecher E.
    Br J Dermatol; 2005 Sep 01; 153(3):635-8. PubMed ID: 16120155
    [Abstract] [Full Text] [Related]

  • 18. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May 01; 105(5):810-24. PubMed ID: 9593380
    [Abstract] [Full Text] [Related]

  • 19. Correlating Adaptive Optics Images to Clinical Findings in Juvenile Macular Dystrophy with Hypotrichosis in Siblings with Homozygous CDH3 Pathogenic Variation.
    Nasser F, Kempf M, Kurtenbach A, Stöhr H, Weber BHF, Neuhaus C, Rating P, Zrenner E.
    Ophthalmic Res; 2020 May 01; 63(2):141-151. PubMed ID: 31927556
    [Abstract] [Full Text] [Related]

  • 20. Early VEP and ERG evidence of visual dysfunction in autosomal recessive osteopetrosis.
    Thompson DA, Kriss A, Taylor D, Russell-Eggitt I, Hodgkins P, Morgan G, Vellodi A, Gerritsen EJ.
    Neuropediatrics; 1998 Jun 01; 29(3):137-44. PubMed ID: 9706624
    [Abstract] [Full Text] [Related]

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