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Journal Abstract Search

318 related items for PubMed ID: 2963026

  • 1.
    ; . PubMed ID:
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  • 2. 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]

  • 3. 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
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  • 6. 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]

  • 7. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.
    Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT.
    Br J Ophthalmol; 2005 Feb; 89(2):198-206. PubMed ID: 15665353
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  • 8. 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]

  • 9. Acute zonal occult outer retinopathy. Donders Lecture: The Netherlands Ophthalmological Society, Maastricht, Holland, June 19, 1992.
    Gass JD.
    J Clin Neuroophthalmol; 1993 Jun; 13(2):79-97. PubMed ID: 8340485
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  • 11. RP cone-rod degeneration.
    Heckenlively JR.
    Trans Am Ophthalmol Soc; 1987 Jun; 85():438-70. PubMed ID: 3447340
    [Abstract] [Full Text] [Related]

  • 12. Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.
    Kondo M, Miyake Y, Kondo N, Ueno S, Takakuwa H, Terasaki H.
    Ophthalmology; 2004 Apr; 111(4):732-9. PubMed ID: 15051206
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  • 13. Restored photoreceptor outer segment damage in multiple evanescent white dot syndrome.
    Li D, Kishi S.
    Ophthalmology; 2009 Apr; 116(4):762-70. PubMed ID: 19344825
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  • 14. Neuro-ophthalmologic features of spinocerebellar ataxia type 7.
    Miller RC, Tewari A, Miller JA, Garbern J, Van Stavern GP.
    J Neuroophthalmol; 2009 Sep; 29(3):180-6. PubMed ID: 19726938
    [Abstract] [Full Text] [Related]

  • 15. Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.
    Lewis CA, Batlle IR, Batlle KG, Banerjee P, Cideciyan AV, Huang J, Alemán TS, Huang Y, Ott J, Gilliam TC, Knowles JA, Jacobson SG.
    Invest Ophthalmol Vis Sci; 1999 Aug; 40(9):2106-14. PubMed ID: 10440267
    [Abstract] [Full Text] [Related]

  • 16. Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).
    Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR.
    Ophthalmology; 2010 Jan; 117(1):120-127.e1. PubMed ID: 19818506
    [Abstract] [Full Text] [Related]

  • 17. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
    Hugosson T, Gränse L, Ponjavic V, Andréasson S.
    Ophthalmic Genet; 2009 Mar; 30(1):1-6. PubMed ID: 19172503
    [Abstract] [Full Text] [Related]

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

  • 19. 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; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 20. Fundus flavimaculatus with severely reduced cone electroretinogram.
    Iijima H, Gohdo T, Hosaka O.
    Jpn J Ophthalmol; 1992 Jun; 36(3):249-56. PubMed ID: 1464966
    [Abstract] [Full Text] [Related]

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