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 *

77 related articles for article (PubMed ID: 1088506)

  • 1. [Study of a family with cone degeneration].
    Malbrel PH; Hache JC; Malbrel C
    Bull Soc Ophtalmol Fr; 1976; 76(7-8):747-51. PubMed ID: 1088506
    [No Abstract]   [Full Text] [Related]  

  • 2. Cone-rod dystrophy: a case report.
    Norden LC; Amos JF; Newcomb RD
    Am J Optom Physiol Opt; 1978 Dec; 55(12):824-35. PubMed ID: 313711
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A clinicopathologic study of a peculiar foveomacular dystrophy.
    Gass JD
    Trans Am Ophthalmol Soc; 1974; 72():139-56. PubMed ID: 4142662
    [No Abstract]   [Full Text] [Related]  

  • 4. [Clinical picture and hereditary transmission of vitelliform degeneration of the macula].
    Thiel HJ; Behnke H
    Klin Monbl Augenheilkd; 1971 Feb; 158(2):235-46. PubMed ID: 5555601
    [No Abstract]   [Full Text] [Related]  

  • 5. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
    Nishiguchi KM; Sandberg MA; Gorji N; Berson EL; Dryja TP
    Hum Mutat; 2005 Mar; 25(3):248-58. PubMed ID: 15712225
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dominant macular degenerations. The cone dystrophies.
    Krill AE; Deutman AF
    Am J Ophthalmol; 1972 Mar; 73(3):352-69. PubMed ID: 4536857
    [No Abstract]   [Full Text] [Related]  

  • 7. [Vitelliform cyst of the macula. Presentation of a case].
    Verraz R
    Arch Sci Med (Torino); 1970; 127(10-12):390-5. PubMed ID: 5519852
    [No Abstract]   [Full Text] [Related]  

  • 8. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
    Auslender N; Sharon D; Abbasi AH; Garzozi HJ; Banin E; Ben-Yosef T
    Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5431-8. PubMed ID: 18055789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Juvenile macular degenerations].
    François J
    Arch Ophtalmol Rev Gen Ophtalmol; 1974; 34(6-7):497-512. PubMed ID: 4142583
    [No Abstract]   [Full Text] [Related]  

  • 11. Color vision defects in pigmentary retinal dystrophy.
    Okajima O; Tanino T; Okamoto M
    Jpn J Ophthalmol; 1982; 26(3):292-301. PubMed ID: 6984101
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.
    Ebenezer ND; Michaelides M; Jenkins SA; Audo I; Webster AR; Cheetham ME; Stockman A; Maher ER; Ainsworth JR; Yates JR; Bradshaw K; Holder GE; Moore AT; Hardcastle AJ
    Invest Ophthalmol Vis Sci; 2005 Jun; 46(6):1891-8. PubMed ID: 15914600
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram.
    Ben Salah S; Kamei S; Sénéćhal A; Lopez S; Bazalgette C; Bazalgette C; Eliaou CM; Zanlonghi X; Hamel CP
    Am J Ophthalmol; 2008 Jun; 145(6):1099-106. PubMed ID: 18400204
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The photoreceptors in cone dystrophies.
    Hansen E
    Mod Probl Ophthalmol; 1974; 13(0):318-27. PubMed ID: 4548148
    [No Abstract]   [Full Text] [Related]  

  • 15. Red contact lenses for alleviation of photophobia in patients with cone disorders.
    Park WL; Sunness JS
    Am J Ophthalmol; 2004 Apr; 137(4):774-5. PubMed ID: 15059731
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Fundus flavimaculatus and dystrophy of the cones].
    Malbrel C; Foltz A; Alame M; Talmud M
    Bull Soc Ophtalmol Fr; 1979; 79(11-12):1099-102. PubMed ID: 317901
    [No Abstract]   [Full Text] [Related]  

  • 17. Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family.
    Van Ghelue M; Eriksen HL; Ponjavic V; Fagerheim T; Andréasson S; Forsman-Semb K; Sandgren O; Holmgren G; Tranebjaerg L
    Ophthalmic Genet; 2000 Dec; 21(4):197-209. PubMed ID: 11135490
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Vitelliform macular degeneration.
    Eriksson AW; Forsius H
    J Genet Hum; 1973 Mar; 21(1):1-13. PubMed ID: 4742120
    [No Abstract]   [Full Text] [Related]  

  • 19. Effects of the beginning of macula degeneration on colour-vision tests.
    Heinsius E
    Mod Probl Ophthalmol; 1972; 11():106-10. PubMed ID: 4544945
    [No Abstract]   [Full Text] [Related]  

  • 20. Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers.
    Ferrell RE; Hittner HM; Chakravarti A
    Am J Med Genet; 1981; 8(3):363-9. PubMed ID: 6940444
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.