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Journal Abstract Search

214 related items for PubMed ID: 2101357

  • 1. ERG characteristics of congenital stationary night blindness.
    Wu D, Xu X, Wu L, Luo T.
    Yan Ke Xue Bao; 1990 Jun; 6(1-2):32-5. PubMed ID: 2101357
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  • 2. [ERG characteristics of congenital stationary night blindness].
    Wu DZ.
    Zhonghua Yan Ke Za Zhi; 1989 Jul; 25(4):203-5. PubMed ID: 2620613
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  • 3. Verifying complaints of difficulties in night vision using electroretinography and dark adaptation tests.
    Allon G, Friedrich Y, Mezer E, Itzhaki A, Leibu R, Perlman I.
    Doc Ophthalmol; 2020 Apr; 140(2):169-180. PubMed ID: 31621038
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  • 5. A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction.
    Barnes CS, Alexander KR, Fishman GA.
    Ophthalmology; 2002 Mar; 109(3):575-83. PubMed ID: 11874764
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  • 7. Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram but not congenital stationary night blindness.
    Tremblay F, De Becker I, Dooley JM, Riddell DC.
    Can J Ophthalmol; 1994 Dec; 29(6):274-9. PubMed ID: 7834566
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  • 11. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
    Noble KG, Carr RE, Siegel IM.
    Am J Ophthalmol; 1990 Jan 15; 109(1):44-8. PubMed ID: 2297031
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  • 12. A form of congenital stationary night blindness with apparent defect of rod phototransduction.
    Peachey NS, Fishman GA, Kilbride PE, Alexander KR, Keehan KM, Derlacki DJ.
    Invest Ophthalmol Vis Sci; 1990 Feb 15; 31(2):237-46. PubMed ID: 2303327
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  • 15. Oscillatory potentials and pattern electroretinogram: are they related?
    Litao RE, Miyake Y, Yagasaki K.
    Jpn J Ophthalmol; 1986 Feb 15; 30(4):402-8. PubMed ID: 3495681
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  • 16. Rod and cone function in the Nougaret form of stationary night blindness.
    Sandberg MA, Pawlyk BS, Dan J, Arnaud B, Dryja TP, Berson EL.
    Arch Ophthalmol; 1998 Jul 15; 116(7):867-72. PubMed ID: 9682699
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  • 19. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
    Scholl HP, Langrová H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E.
    Invest Ophthalmol Vis Sci; 2001 Oct 15; 42(11):2728-36. PubMed ID: 11581222
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  • 20. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2001 Jun 15; 42(7):1610-6. PubMed ID: 11381068
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