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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 8015786)

  • 41. Hereditary pigmented paravenous chorioretinal atrophy.
    Noble KG
    Am J Ophthalmol; 1989 Oct; 108(4):365-9. PubMed ID: 2801856
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.
    Edwards AO; Miedziak A; Vrabec T; Verhoeven J; Acott TS; Weleber RG; Donoso LA
    Am J Ophthalmol; 1999 Apr; 127(4):426-35. PubMed ID: 10218695
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Dark choroid in cone-rod dystrophy.
    Leys A; Van De Sompel W
    Eur J Ophthalmol; 1992; 2(1):39-40. PubMed ID: 1638166
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Unilateral acute posterior multifocal placoid pigment epitheliopathy.
    Nakajima N; Noda S; Hayasaka S
    Ophthalmologica; 1996; 210(2):123-5. PubMed ID: 8859489
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Multifocal chorioretinal lesions in Borzoi dogs.
    Storey ES; Grahn BH; Alcorn J
    Vet Ophthalmol; 2005; 8(5):337-47. PubMed ID: 16178845
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1.
    Kellner S; Stöhr H; Fiebig B; Weinitz S; Farmand G; Kellner U; Weber BH
    Ophthalmic Genet; 2016 Jun; 37(2):201-8. PubMed ID: 26771239
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [A new approach for studying the retinal and choroidal circulation].
    Yoneya S
    Nippon Ganka Gakkai Zasshi; 2004 Dec; 108(12):836-61; discussion 862. PubMed ID: 15656089
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Dominant cystoid macular dystrophy.
    Saksens NT; van Huet RA; van Lith-Verhoeven JJ; den Hollander AI; Hoyng CB; Boon CJ
    Ophthalmology; 2015 Jan; 122(1):180-91. PubMed ID: 25267528
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Evolution of age-related macular degeneration with choroidal perfusion abnormality.
    Piguet B; Palmvang IB; Chisholm IH; Minassian D; Bird AC
    Am J Ophthalmol; 1992 Jun; 113(6):657-63. PubMed ID: 1598956
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Long-term follow-up of dominant macular dystrophy with flecks (Stargardt).
    Mansour AM
    Ophthalmologica; 1992; 205(3):138-43. PubMed ID: 1475092
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Idiopathic polypoidal choroidal vasculopathy of the macula.
    Moorthy RS; Lyon AT; Rabb MF; Spaide RF; Yannuzzi LA; Jampol LM
    Ophthalmology; 1998 Aug; 105(8):1380-5. PubMed ID: 9709746
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Central areolar choroidal dystrophy.
    Noble KG
    Am J Ophthalmol; 1977 Sep; 84(3):310-8. PubMed ID: 900227
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Serpiginous choroidopathy--spectrum of fundus changes in 3 years of follow up].
    Wyrwicka A; Jurowski P
    Klin Oczna; 2010; 112(1-3):53-6. PubMed ID: 20572505
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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; 134(9):992-1000. PubMed ID: 27386845
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Report of a novel lobular chorioretinal dystrophy.
    Moradi P; Lotery A
    Eye (Lond); 2006 Dec; 20(12):1390-2. PubMed ID: 16456598
    [No Abstract]   [Full Text] [Related]  

  • 56. Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.
    Stone EM; Nichols BE; Kimura AE; Weingeist TA; Drack A; Sheffield VC
    Arch Ophthalmol; 1994 Jun; 112(6):765-72. PubMed ID: 8002834
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 59. Adult vitelliform macular dystrophy.
    Brecher R; Bird AC
    Eye (Lond); 1990; 4 ( Pt 1)():210-5. PubMed ID: 2323472
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Multifocal electroretinogram and central visual field testing in central areolar choroidal dystrophy.
    Gundogan FC; Dinç UA; Erdem U; Ozge G; Sobaci G
    Eur J Ophthalmol; 2010; 20(5):919-24. PubMed ID: 20306439
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.