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Journal Abstract Search

156 related items for PubMed ID: 14661912

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  • 26. Full-field electroretinogram in autism spectrum disorder.
    Constable PA, Gaigg SB, Bowler DM, Jägle H, Thompson DA.
    Doc Ophthalmol; 2016 Apr; 132(2):83-99. PubMed ID: 26868825
    [Abstract] [Full Text] [Related]

  • 27. Electroretinographic characteristics in children with infantile nystagmus syndrome and early-onset retinal dystrophies.
    Kurent A, Stirn-Kranjc B, Brecelj J.
    Eur J Ophthalmol; 2015 Apr; 25(1):33-42. PubMed ID: 25096283
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  • 28. 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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  • 29. Night blindness with depolarizing pattern of ON/OFF response in electroretinogram: a case report.
    Usui T, Tanimoto N, Ueki S, Miki A, Takagi M, Hasegawa S, Abe H.
    Doc Ophthalmol; 2005 Jul; 111(1):15-21. PubMed ID: 16502303
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  • 30. The negative ERG is not synonymous with nightblindness.
    Cibis GW, Fitzgerald KM.
    Trans Am Ophthalmol Soc; 2001 Jul; 99():171-5; discussion 175-6. PubMed ID: 11797304
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  • 31. [Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].
    Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2002 Dec; 106(12):737-55; discussion 756. PubMed ID: 12610835
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  • 32. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
    Oh A, Loew ER, Foster ML, Davidson MG, English RV, Gervais KJ, Herring IP, Mowat FM.
    Doc Ophthalmol; 2018 Oct; 137(2):87-101. PubMed ID: 30051304
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  • 33. TRPM1 mutations are associated with the complete form of congenital stationary night blindness.
    Nakamura M, Sanuki R, Yasuma TR, Onishi A, Nishiguchi KM, Koike C, Kadowaki M, Kondo M, Miyake Y, Furukawa T.
    Mol Vis; 2010 Mar 12; 16():425-37. PubMed ID: 20300565
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  • 34. 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 12; 29(6):274-9. PubMed ID: 7834566
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  • 35. Electrophysiological findings in patients with Oguchi's disease.
    Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A.
    Jpn J Ophthalmol; 1996 Dec 12; 40(4):511-9. PubMed ID: 9130055
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  • 36. Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
    Bech-Hansen NT, Pearce WG.
    Am J Hum Genet; 1993 Jan 12; 52(1):71-7. PubMed ID: 8434607
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  • 37. Abnormalities of the photoreceptor-bipolar cell synapse in a substrain of C57BL/10 mice.
    Ruether K, Grosse J, Matthiessen E, Hoffmann K, Hartmann C.
    Invest Ophthalmol Vis Sci; 2000 Nov 12; 41(12):4039-47. PubMed ID: 11053310
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  • 38. Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
    Neuillé M, Malaichamy S, Vadalà M, Michiels C, Condroyer C, Sachidanandam R, Srilekha S, Arokiasamy T, Letexier M, Démontant V, Sahel JA, Sen P, Audo I, Soumittra N, Zeitz C.
    Clin Genet; 2016 Jun 12; 89(6):690-9. PubMed ID: 26822852
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  • 39. 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 12; 140(2):169-180. PubMed ID: 31621038
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  • 40. 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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