These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


181 related items for PubMed ID: 1085161

  • 21. [Hereditary macular degenerations].
    Jaeger W, Alexandridis E, Kraus E, Tenner A, Käfer O.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975; (73):695-735. PubMed ID: 1106398
    [No Abstract] [Full Text] [Related]

  • 22. [The fluorescein angiogram in choroidermia (author's transl)].
    Hammerstein W, Leide E, Bischof G.
    Klin Monbl Augenheilkd; 1977 Oct; 171(4):592-6. PubMed ID: 304118
    [Abstract] [Full Text] [Related]

  • 23. Bilateral giant macular schisis in a case of Goldmann-Favre syndrome.
    Chawla R, Banerjee M.
    BMJ Case Rep; 2019 Sep 26; 12(9):. PubMed ID: 31558488
    [Abstract] [Full Text] [Related]

  • 24. Abnormal findings relatives of patients with juvenile hereditary macular degeneration (Stargardt's disease).
    Merin S, Landau J.
    Ophthalmologica; 1970 Sep 26; 161(1):1-10. PubMed ID: 5432144
    [No Abstract] [Full Text] [Related]

  • 25. Modern concepts of senile macular degeneration.
    Kornzweig AL.
    J Am Geriatr Soc; 1974 Jun 26; 22(6):246-53. PubMed ID: 4599018
    [No Abstract] [Full Text] [Related]

  • 26. Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus).
    Sergouniotis PI, Sohn EH, Li Z, McBain VA, Wright GA, Moore AT, Robson AG, Holder GE, Webster AR.
    Ophthalmology; 2011 Aug 26; 118(8):1661-70. PubMed ID: 21529959
    [Abstract] [Full Text] [Related]

  • 27. Diagnostic and therapeutic challenges.
    McDonald HR.
    Retina; 2000 Aug 26; 20(1):86-9. PubMed ID: 10696754
    [No Abstract] [Full Text] [Related]

  • 28. Snowflake degeneration in hereditary vitreoretinal degeneration.
    Hirose T, Lee KY, Schepens CL.
    Am J Ophthalmol; 1974 Feb 26; 77(2):143-53. PubMed ID: 4812083
    [No Abstract] [Full Text] [Related]

  • 29. Familial foveal retinoschisis associated with a rod-cone dystrophy.
    Noble KG, Carr RE, Siegel IM.
    Am J Ophthalmol; 1978 Apr 26; 85(4):551-7. PubMed ID: 306756
    [Abstract] [Full Text] [Related]

  • 30. Relatively enhanced S cone function in the Goldmann-Favre syndrome.
    Jacobson SG, Román AJ, Román MI, Gass JD, Parker JA.
    Am J Ophthalmol; 1991 Apr 15; 111(4):446-53. PubMed ID: 2012146
    [Abstract] [Full Text] [Related]

  • 31. Novel findings in enhanced S-cone syndrome: a case with macular retinal neovascularization and severe retinal vasculitis.
    Bazvand F, Khojasteh H, Zarei M.
    Doc Ophthalmol; 2019 Dec 15; 139(3):221-226. PubMed ID: 31292819
    [Abstract] [Full Text] [Related]

  • 32. Stargardt's hereditary progressive macular degeneration.
    Irvine AR, Wergeland FL.
    Br J Ophthalmol; 1972 Nov 15; 56(11):817-26. PubMed ID: 4647131
    [No Abstract] [Full Text] [Related]

  • 33. [Goldmann-Favre hyaloido-tapetoretinal degeneration].
    Fiore C, Ricci A.
    Arch Ophtalmol (Paris); 1976 Feb 15; 36(2):127-36. PubMed ID: 132917
    [Abstract] [Full Text] [Related]

  • 34. Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition.
    Jalili IK.
    J Med Genet; 1989 Aug 15; 26(8):504-10. PubMed ID: 2769722
    [Abstract] [Full Text] [Related]

  • 35. Retinal degeneration in a baboon.
    Vainisi SJ, Beck BB, Apple DJ.
    Am J Ophthalmol; 1974 Aug 15; 78(2):279-84. PubMed ID: 4211191
    [No Abstract] [Full Text] [Related]

  • 36. [A fundus flavimaculatus associated with preretinal new vessels (author's transl)].
    Coscas G, Gaudric A, Barthelemy F.
    J Fr Ophtalmol; 1980 Feb 20; 3(1):27-31. PubMed ID: 6154728
    [Abstract] [Full Text] [Related]

  • 37. High-definition optical coherence tomographic visualization of photoreceptor layer and retinal flecks in fundus albipunctatus associated with cone dystrophy.
    Querques G, Carrillo P, Querques L, Bux AV, Del Curatolo MV, Delle Noci N.
    Arch Ophthalmol; 2009 May 20; 127(5):703-6. PubMed ID: 19433727
    [No Abstract] [Full Text] [Related]

  • 38. [Hereditary macular degenerations].
    François J.
    Ophthalmologica; 1974 May 20; 168(6):417-45. PubMed ID: 4603577
    [No Abstract] [Full Text] [Related]

  • 39. The diagnostic importance of functional electrooculography in some hereditary dystrophies of the eye fundus.
    François J.
    Ann Ophthalmol; 1971 Sep 20; 3(9):929-46. PubMed ID: 4950484
    [No Abstract] [Full Text] [Related]

  • 40. Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
    Sharon D, Sandberg MA, Caruso RC, Berson EL, Dryja TP.
    Arch Ophthalmol; 2003 Sep 20; 121(9):1316-23. PubMed ID: 12963616
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 10.