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 *

113 related articles for article (PubMed ID: 854266)

  • 1. Peripheral cone disease.
    Pinckers A; Deutman AF
    Ophthalmologica; 1977; 174(3):145-50. PubMed ID: 854266
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Progressive generalized cone dysfunction.
    François J; de Rouck A; Verriest G; de Laey JJ; Cambie E
    Ophthalmologica; 1974; 169(4):255-84. PubMed ID: 4547582
    [No Abstract]   [Full Text] [Related]  

  • 3. The cone degenerations.
    Krill AE; Deutman AF; Fishman M
    Doc Ophthalmol; 1973 Apr; 35(1):1-80. PubMed ID: 4573331
    [No Abstract]   [Full Text] [Related]  

  • 4. High myopia with cone dysfunction.
    Mäntyjärvi M; Katajakunnas M; Vänttinen S
    Acta Ophthalmol (Copenh); 1991 Apr; 69(2):155-61. PubMed ID: 1872133
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An electroretinographic and molecular genetic study of X-linked cone degeneration.
    Reichel E; Bruce AM; Sandberg MA; Berson EL
    Am J Ophthalmol; 1989 Nov; 108(5):540-7. PubMed ID: 2554733
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cone dystrophies: clinical and electrophysiological findings.
    Kellner U; Kleine-Hartlage P; Foerster MH
    Ger J Ophthalmol; 1992; 1(2):105-9. PubMed ID: 1477624
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Progressive peripheral cone dysfunction.
    Noble KG; Siegel IM; Carr RE
    Am J Ophthalmol; 1988 Nov; 106(5):557-60. PubMed ID: 3189471
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Differential diagnosis of cone dystrophies].
    Sadowski B; Zrenner E
    Ophthalmologe; 1994 Dec; 91(6):719-29. PubMed ID: 7849422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Progressive cone dystrophy.
    Ripps H; Noble KG; Greenstein VC; Siegel IM; Carr RE
    Ophthalmology; 1987 Nov; 94(11):1401-9. PubMed ID: 3684214
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxia.
    Hamilton SR; Chatrian GE; Mills RP; Kalina RE; Bird TD
    Arch Ophthalmol; 1990 Apr; 108(4):551-6. PubMed ID: 2322158
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [Adaptational changes in human cone flicker electroretinogram].
    Ota I; Shiroyama N; Horiguchi M; Miyake Y
    Nippon Ganka Gakkai Zasshi; 1988 Mar; 92(3):549-56. PubMed ID: 3414469
    [No Abstract]   [Full Text] [Related]  

  • 14. Cone-rod dysfunction in patients with unexplained reduction in visual acuity.
    Lang Y; Leibu R; Garzuzi H; Perlman I
    Doc Ophthalmol; 1996-1997; 92(3):173-91. PubMed ID: 9181345
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.
    Mizrahi-Meissonnier L; Merin S; Banin E; Sharon D
    Invest Ophthalmol Vis Sci; 2010 Aug; 51(8):3884-92. PubMed ID: 20220053
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rod visual fields in cone-rod degeneration. Comparisons to retinitis pigmentosa.
    Birch DG; Anderson JL
    Invest Ophthalmol Vis Sci; 1990 Nov; 31(11):2288-99. PubMed ID: 2242994
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Progressive cone dystrophies.
    François J; De Rouck A; De Laey JJ
    Ophthalmologica; 1976; 173(2):81-101. PubMed ID: 1066593
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked cone dystrophy.
    Verdoorn C; Pinckers A
    Doc Ophthalmol; 1988; 70(2-3):195-8. PubMed ID: 3234184
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Retinal degeneration with blue cone hypersensitivity].
    Kellner U; Foerster MH
    Fortschr Ophthalmol; 1991; 88(6):637-41. PubMed ID: 1794782
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Selective cone dystrophy with protan genotype.
    Kellner U; Sadowski B; Zrenner E; Foerster MH
    Invest Ophthalmol Vis Sci; 1995 Nov; 36(12):2381-7. PubMed ID: 7591627
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.