BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 8152765)

  • 61. Pathology of hereditary juvenile retinoschisis.
    Manschot WA
    Arch Ophthalmol; 1972 Aug; 88(2):131-8. PubMed ID: 5054298
    [No Abstract]   [Full Text] [Related]  

  • 62. Gravity-dependent distribution of retinal pigment epithelial cells dispersed into the vitreous cavity.
    Singh AK; Glaser BM; Lemor M; Michels RG
    Retina; 1986; 6(2):77-80. PubMed ID: 3749624
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Variable phenotype of Knobloch syndrome due to biallelic
    Levinger N; Hendler K; Banin E; Hanany M; Kimchi A; Mechoulam H; Meiner V; Parag Y; Sharon D; Macarov M; Yahalom C
    Eur J Ophthalmol; 2021 Nov; 31(6):3349-3354. PubMed ID: 33238767
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Idiopathic serous detachment of the retinal pigment epithelium.
    Lewis ML
    Arch Ophthalmol; 1978 Apr; 96(4):620-4. PubMed ID: 646687
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Molecular and Clinical Findings in Patients With Knobloch Syndrome.
    Hull S; Arno G; Ku CA; Ge Z; Waseem N; Chandra A; Webster AR; Robson AG; Michaelides M; Weleber RG; Davagnanam I; Chen R; Holder GE; Pennesi ME; Moore AT
    JAMA Ophthalmol; 2016 Jul; 134(7):753-62. PubMed ID: 27259167
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Pigment epithelial pattern dystrophy. Four different manifestations in a family.
    de Jong PT; Delleman JW
    Arch Ophthalmol; 1982 Sep; 100(9):1416-21. PubMed ID: 7115165
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Autosomal dominant vitreoretinochoroidopathy.
    Roider J; Fritsch E; Hoerauf H; Heide W; Laqua H
    Retina; 1997; 17(4):294-9. PubMed ID: 9279944
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Inhibition of retinal pigment epithelial cell-induced tractional retinal detachment by disintegrins, a group of Arg-Gly-Asp-containing peptides from viper venom.
    Yang CH; Huang TF; Liu KR; Chen MS; Hung PT
    Invest Ophthalmol Vis Sci; 1996 Apr; 37(5):843-54. PubMed ID: 8603869
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.
    Michaelides M; Wilkie SE; Jenkins S; Holder GE; Hunt DM; Moore AT; Webster AR
    Ophthalmology; 2005 Aug; 112(8):1442-7. PubMed ID: 15953638
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Dissociation of rod and cone sensitivity by acute localized retinal pigment epithelium loss.
    Krøyer K; la Cour M; Larsen M
    Acta Ophthalmol; 2008 May; 86(3):338-40. PubMed ID: 17662094
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Pathogenesis and classification of massive periretinal proliferation.
    Machemer R
    Br J Ophthalmol; 1978 Nov; 62(11):737-47. PubMed ID: 102335
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Prophylactic laser photocoagulation in hereditary snowflake vitreoretinal degeneration. A family report.
    Pollack A; Uchenik D; Chemke J; Oliver M
    Arch Ophthalmol; 1983 Oct; 101(10):1536-9. PubMed ID: 6626003
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Retinal topography and thickness mapping in atrophic age related macular degeneration.
    Shahidi M; Blair NP; Mori M; Gieser J; Pulido JS
    Br J Ophthalmol; 2002 Jun; 86(6):623-6. PubMed ID: 12034682
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Ophthalmologic findings in a patient with cerebellar ataxia, hypogonadotropic hypogonadism, and chorioretinal dystrophy.
    Salvador F; García-Arumí J; Corcóstegui B; Minoves T; Tarrus F
    Am J Ophthalmol; 1995 Aug; 120(2):241-4. PubMed ID: 7639308
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Central areolar pigment epithelial dystrophy.
    Fetkenhour CL; Gurney N; Dobbie JG; Choromokos E
    Am J Ophthalmol; 1976 Jun; 81(6):745-53. PubMed ID: 937428
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.
    Gregory-Evans K; Kelsell RE; Gregory-Evans CY; Downes SM; Fitzke FW; Holder GE; Simunovic M; Mollon JD; Taylor R; Hunt DM; Bird AC; Moore AT
    Ophthalmology; 2000 Jan; 107(1):55-61. PubMed ID: 10647719
    [TBL] [Abstract][Full Text] [Related]  

  • 77. The distinct ophthalmic phenotype of Knobloch syndrome in children.
    Khan AO; Aldahmesh MA; Mohamed JY; Al-Mesfer S; Alkuraya FS
    Br J Ophthalmol; 2012 Jun; 96(6):890-5. PubMed ID: 22399687
    [TBL] [Abstract][Full Text] [Related]  

  • 78. [Which abnormalities can be detected in myopic peripheral retina?].
    Berrod JP; Hubert I
    J Fr Ophtalmol; 2012 May; 35(5):378-86. PubMed ID: 22521740
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Autosomal dominant pericentral retinochoroidal atrophy.
    Bass SJ; Noble KG
    Retina; 2006 Jan; 26(1):71-9. PubMed ID: 16395142
    [TBL] [Abstract][Full Text] [Related]  

  • 80. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.