BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 3698795)

  • 1. Statistical evaluation of visual functions in dominant and recessive autosomal pigmentary retinopathy.
    De Rouck A; de Bie S; Kayembe D
    Doc Ophthalmol; 1986 Mar; 62(3):265-80. PubMed ID: 3698795
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive pericentral pigmentary retinopathy.
    Traboulsi EI; O'Neill JF; Maumenee IH
    Am J Ophthalmol; 1988 Nov; 106(5):551-6. PubMed ID: 3189470
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Retinitis pigmentosa. Visual loss.
    Fishman GA
    Arch Ophthalmol; 1978 Jul; 96(7):1185-8. PubMed ID: 307377
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The electroretinogram in retinitis pigmentosa.
    Marmor MF
    Arch Ophthalmol; 1979 Jul; 97(7):1300-4. PubMed ID: 454267
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Visual prognosis of retinitis pigmentosa].
    Sakaguchi E
    Nippon Ganka Gakkai Zasshi; 1984 Jun; 88(6):983-90. PubMed ID: 6475679
    [No Abstract]   [Full Text] [Related]  

  • 6. A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa.
    Grover S; Fishman GA; Anderson RJ; Lindeman M
    Ophthalmology; 2000 Feb; 107(2):386-96. PubMed ID: 10690843
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sector retinitis pigmentosa.
    Krill AE; Archer D; Martin D
    Am J Ophthalmol; 1970 Jun; 69(6):977-87. PubMed ID: 5423778
    [No Abstract]   [Full Text] [Related]  

  • 8. Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2D.
    Stunkel ML; Brodie SE; Cideciyan AV; Pfeifer WL; Kennedy EL; Stone EM; Jacobson SG; Drack AV
    Am J Ophthalmol; 2018 Jun; 190():58-68. PubMed ID: 29559409
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical measures of visual function in familial retinitis pigmentosa.
    Williams TD; Lovasik JV
    Am J Optom Physiol Opt; 1985 Jan; 62(1):45-51. PubMed ID: 3976835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal dominant retinitis pigmentosa. A method of classification.
    Fishman GA; Alexander KR; Anderson RJ
    Arch Ophthalmol; 1985 Mar; 103(3):366-74. PubMed ID: 3977711
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Genetic aspects in pigmentary retinopathy].
    Preoteasa D
    Oftalmologia; 1996; 40(2):137-44. PubMed ID: 8717081
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient.
    Hayakawa M; Hotta Y; Imai Y; Fujiki K; Nakamura A; Yanashima K; Kanai A
    Am J Ophthalmol; 1993 Feb; 115(2):168-73. PubMed ID: 7679248
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sector retinitis pigmentosa. Electrophysiological and psychophysical study of the visual system.
    Abraham FA
    Doc Ophthalmol; 1975 Nov; 39(1):13-28. PubMed ID: 1201696
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Electrophysiological study on the retinitis pigmentosa].
    Imaizumi K
    Nippon Ganka Gakkai Zasshi; 1969 Nov; 73(11):2347-496. PubMed ID: 5391946
    [No Abstract]   [Full Text] [Related]  

  • 15. Clinical and electrophysiological observations on genetic carriers of retinitis pigmentosa in a family (pedigree Tt) showing sex-linked inheritance.
    Imaizumi K; Takahashi R; Tazawa Y; Yamada K; Mita K
    Adv Exp Med Biol; 1972; 24(0):301-7. PubMed ID: 4671885
    [No Abstract]   [Full Text] [Related]  

  • 16. Atypical sector pigmentary dystrophy.
    Pinckers A; Greydanus J; Deutman AF; Duinkerke-Eerola KU
    Int Ophthalmol; 1986 May; 9(2-3):143-9. PubMed ID: 3721715
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Visual Function in Carriers of X-Linked Retinitis Pigmentosa.
    Comander J; Weigel-DiFranco C; Sandberg MA; Berson EL
    Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa.
    Fishman GA; Stone EM; Sheffield VC; Gilbert LD; Kimura AE
    Arch Ophthalmol; 1992 Jan; 110(1):54-62. PubMed ID: 1731723
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Variability of visual acuity, dark adaptation and electroretinogram in retinitis pigmentosa].
    Niemeyer G; Gurewitsch K
    Klin Monbl Augenheilkd; 1982 May; 180(5):401-4. PubMed ID: 7109486
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cone and rod ERG phototransduction parameters in retinitis pigmentosa.
    Tzekov RT; Locke KG; Hood DC; Birch DG
    Invest Ophthalmol Vis Sci; 2003 Sep; 44(9):3993-4000. PubMed ID: 12939320
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.