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    Results: 1 to 20 of 375

    1.

    Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.

    Kabanarou SA, Holder GE, Fitzke FW, Bird AC, Webster AR.

    Br J Ophthalmol. 2004 Aug;88(8):1018-22.PMID: 15258017 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    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;116(7):867-72.PMID: 9682699 [PubMed - indexed for MEDLINE]Related articles

    3.

    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.PMID: 2297031 [PubMed - indexed for MEDLINE]Related articles

    4.

    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.PMID: 11874764 [PubMed - indexed for MEDLINE]Related articles

    5.

    Cone function in congenital nyctalopia.

    Siegel IM, Greenstein VC, Seiple WH, Carr RE.

    Doc Ophthalmol. 1987 Mar;65(3):307-18.PMID: 3500024 [PubMed - indexed for MEDLINE]Related articles

    6.

    A dominant form of congenital stationary night blindness (adCSNB) in a large Chinese family.

    Liu X, Zhuang S, Hu S, Zhang F, Lin B, Li X, Xu D, Chen SH.

    Ann Hum Genet. 2005 May;69(Pt 3):315-21.PMID: 15845035 [PubMed - indexed for MEDLINE]Related articles

    7.

    [Congenital stationary night blindness]

    Svĕrák J, Jebavá R, Peregrin J, Zizka J, Hartmann M.

    Cesk Slov Oftalmol. 1996 Jul;52(3):135-42. Czech. PMID: 8768469 [PubMed - indexed for MEDLINE]Related articles

    8.

    Evidence supportive of a functional discrimination between photopic oscillatory potentials as revealed with cone and rod mediated retinopathies.

    Lachapelle P, Rousseau S, McKerral M, Benoit J, Polomeno RC, Koenekoop RK, Little JM.

    Doc Ophthalmol. 1998;95(1):35-54.PMID: 10189180 [PubMed - indexed for MEDLINE]Related articles

    9.

    Congenital stationary night blindness with negative electroretinogram. A new classification.

    Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T.

    Arch Ophthalmol. 1986 Jul;104(7):1013-20.PMID: 3488053 [PubMed - indexed for MEDLINE]Related articles

    10.

    Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

    Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.

    Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4328-35.PMID: 16249515 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    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;31(2):237-46.PMID: 2303327 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity.

    Hayakawa M, Imai Y, Wakita M, Kato K, Yanashima K, Miyake Y, Kanai A.

    Ophthalmic Paediatr Genet. 1992 Dec;13(4):211-7.PMID: 1488221 [PubMed - indexed for MEDLINE]Related articles

    13.

    Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.

    Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E.

    Vision Res. 2002 May;42(11):1475-83.PMID: 12044753 [PubMed - indexed for MEDLINE]Related articles

    14.

    ERGs in female carriers of incomplete congenital stationary night blindness (I-CSNB). A family report.

    Rigaudière F, Roux C, Lachapelle P, Rosolen SG, Bitoun P, Gay-Duval A, Le Gargasson JF.

    Doc Ophthalmol. 2003 Sep;107(2):203-12.PMID: 14661912 [PubMed - indexed for MEDLINE]Related articles

    15.

    Electrophysiological findings in patients with Oguchi's disease.

    Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A.

    Jpn J Ophthalmol. 1996;40(4):511-9.PMID: 9130055 [PubMed - indexed for MEDLINE]Related articles

    16.

    Scotopic threshold response in complete and incomplete types of congenital stationary night blindness.

    Miyake Y, Horiguchi M, Terasaki H, Kondo M.

    Invest Ophthalmol Vis Sci. 1994 Sep;35(10):3770-5.PMID: 8088964 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Acquired unilateral night blindness associated with a negative electroretinogram waveform.

    Fishman GA, Alexander KR, Milam AH, Derlacki DJ.

    Ophthalmology. 1996 Jan;103(1):96-104.PMID: 8628566 [PubMed - indexed for MEDLINE]Related articles

    18.

    The negative ERG is not synonymous with nightblindness.

    Cibis GW, Fitzgerald KM.

    Trans Am Ophthalmol Soc. 2001;99:171-5; discussion 175-6.PMID: 11797304 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.

    Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT.

    Br J Ophthalmol. 2005 Feb;89(2):198-206.PMID: 15665353 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    [Clinical findings in autosomal recessive syndrome of blue cone hypersensitivity]

    Jurklies B, Weismann M, Kellner U, Zrenner E, Bornfeld N.

    Ophthalmologe. 2001 Mar;98(3):285-93. German. PMID: 11320818 [PubMed - indexed for MEDLINE]Related articles

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