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Journal Abstract Search

437 related items for PubMed ID: 15636262

  • 1. [Electroretinogram and electrooculogram in a family with Stargardt's disease].
    Pojda-Wilczek D, Makowiecka-Obidzińska K, Herba E.
    Klin Oczna; 2004; 106(3 Suppl):540-1. PubMed ID: 15636262
    [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. Cone dystrophies: clinical and electrophysiological findings.
    Kellner U, Kleine-Hartlage P, Foerster MH.
    Ger J Ophthalmol; 1992 Mar; 1(2):105-9. PubMed ID: 1477624
    [Abstract] [Full Text] [Related]

  • 4. [Stargardt's disease (ERG, EOG and chromatic sense)].
    Pinckers A.
    Ann Ocul (Paris); 1971 Dec; 204(12):1331-46. PubMed ID: 5150321
    [No Abstract] [Full Text] [Related]

  • 5. Bull's-eye maculopathy and negative electroretinogram.
    Miyake Y, Shiroyama N, Horiguchi M, Saito A, Yagasaki K.
    Retina; 1989 Dec; 9(3):210-5. PubMed ID: 2595114
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Visual rehabilitation of patients with Stargardt's disease.
    Shah M, Zaman M, Khan MT, Khan MD.
    J Coll Physicians Surg Pak; 2008 May; 18(5):294-8. PubMed ID: 18541085
    [Abstract] [Full Text] [Related]

  • 8. Initial rapid decrease in visual acuity in siblings with Stargardt's disease.
    Hayasaka S, Kurome H, Noda S, Mihara M.
    Jpn J Ophthalmol; 1993 May; 37(4):485-9. PubMed ID: 8145394
    [Abstract] [Full Text] [Related]

  • 9. 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; 105(5):810-24. PubMed ID: 9593380
    [Abstract] [Full Text] [Related]

  • 10. 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 May; 110(4-6):188-92. PubMed ID: 18655459
    [Abstract] [Full Text] [Related]

  • 11. [ERG diagnosis and differential diagnosis: results of examination over 6 years].
    Stemeyer G, Stähli P.
    Klin Monbl Augenheilkd; 1996 May; 208(5):306-10. PubMed ID: 8766035
    [Abstract] [Full Text] [Related]

  • 12. [Acute macular neuroretinopathy--case report].
    Pojda-Wilczek D, Herba E.
    Klin Oczna; 2005 May; 107(1-3):127-9. PubMed ID: 16052823
    [Abstract] [Full Text] [Related]

  • 13. Japanese family with blue cone monochromatism.
    Terasaki H, Miyake Y.
    Jpn J Ophthalmol; 1992 May; 36(2):132-41. PubMed ID: 1513061
    [Abstract] [Full Text] [Related]

  • 14. 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; 113(11):2066.e1-10. PubMed ID: 16935340
    [Abstract] [Full Text] [Related]

  • 15. 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; 112(4):586-92. PubMed ID: 15808248
    [Abstract] [Full Text] [Related]

  • 16. [Electroretinogram and electrooculogram in retinal degeneration].
    Pojda-Wilczek D.
    Klin Oczna; 1999 Apr; 101(6):481-5. PubMed ID: 10786061
    [Abstract] [Full Text] [Related]

  • 17. Electrophysiological findings in Stargardt's-fundus flavimaculatus disease.
    Stavrou P, Good PA, Misson GP, Kritzinger EE.
    Eye (Lond); 1998 Apr; 12 ( Pt 6)():953-8. PubMed ID: 10325994
    [Abstract] [Full Text] [Related]

  • 18. Dominant inheritance of Stargardt's disease.
    Bither PP, Berns LA.
    J Am Optom Assoc; 1988 Feb; 59(2):112-7. PubMed ID: 3361050
    [Abstract] [Full Text] [Related]

  • 19. Foveal cone dysfunction syndrome.
    ten Hove MW, Siatkowski RM, Smith JL.
    J Neuroophthalmol; 1998 Mar; 18(1):9-14. PubMed ID: 9532531
    [Abstract] [Full Text] [Related]

  • 20. [Routine monitoring of patients treated with synthetic antimalarials].
    Douche C, Bechetoille A, Ebran JM.
    J Fr Ophtalmol; 1983 Mar; 6(8-9):689-95. PubMed ID: 6677659
    [Abstract] [Full Text] [Related]

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