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Journal Abstract Search

454 related items for PubMed ID: 30051304

  • 1. 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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  • 2. In vivo electroretinographic differentiation of rod, short-wavelength and long/medium-wavelength cone responses in dogs using silent substitution stimuli.
    Mowat FM, Wise E, Oh A, Foster ML, Kremers J.
    Exp Eye Res; 2019 Aug; 185():107673. PubMed ID: 31128103
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  • 3. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
    Marmor MF, Zeitz C.
    Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
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  • 4. Differentiation of murine models of "negative ERG" by single and repetitive light stimuli.
    Tanimoto N, Akula JD, Fulton AB, Weber BH, Seeliger MW.
    Doc Ophthalmol; 2016 Apr; 132(2):101-9. PubMed ID: 26996188
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  • 5. A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.
    Kondo M, Das G, Imai R, Santana E, Nakashita T, Imawaka M, Ueda K, Ohtsuka H, Sakai K, Aihara T, Kato K, Sugimoto M, Ueno S, Nishizawa Y, Aguirre GD, Miyadera K.
    PLoS One; 2015 Apr; 10(9):e0137072. PubMed ID: 26368928
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  • 8. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
    Al Oreany AA, Al Hadlaq A, Schatz P.
    Graefes Arch Clin Exp Ophthalmol; 2016 Oct; 254(10):1951-1956. PubMed ID: 27084085
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  • 9. Disinhibition of intrinsic photosensitive retinal ganglion cells in patients with X-linked congenital stationary night blindness.
    Schatz A, Kelbsch C, Zeitz C, Kohl S, Zrenner E, Gekeler F, Wilhelm H, Wilhelm B, Willmann G.
    Graefes Arch Clin Exp Ophthalmol; 2019 Jun; 257(6):1207-1215. PubMed ID: 30982101
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  • 10. Electronegative Electroretinograms in the United Arab Emirates.
    Alsalamah AK, Khan AO.
    Middle East Afr J Ophthalmol; 2020 Jun; 27(2):86-90. PubMed ID: 32874040
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  • 14. Complete congenital stationary night blindness associated with a novel NYX variant (p.Asn216Lys) in middle-aged and older adult patients.
    Hayashi T, Murakami Y, Mizobuchi K, Koyanagi Y, Sonoda KH, Nakano T.
    Ophthalmic Genet; 2021 Aug; 42(4):412-419. PubMed ID: 33769208
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  • 15. Behavioral phenotypic properties of a natural occurring rat model of congenital stationary night blindness with Cacna1f mutation.
    An J, Wang L, Guo Q, Li L, Xia F, Zhang Z.
    J Neurogenet; 2012 Sep; 26(3-4):363-73. PubMed ID: 22800190
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  • 16. Extracting the ON and OFF contributions to the full-field photopic flash electroretinogram using summed growth curves.
    Akula JD, Ambrosio L, Howard FI, Hansen RM, Fulton AB.
    Exp Eye Res; 2019 Dec; 189():107827. PubMed ID: 31600486
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  • 17. A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
    Sergouniotis PI, Robson AG, Li Z, Devery S, Holder GE, Moore AT, Webster AR.
    Acta Ophthalmol; 2012 May; 90(3):e192-7. PubMed ID: 22008250
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  • 18. Long-term follow-up of retinal function and structure in TRPM1-associated complete congenital stationary night blindness.
    Al-Hujaili H, Taskintuna I, Neuhaus C, Bergmann C, Schatz P.
    Mol Vis; 2019 May; 25():851-858. PubMed ID: 31908403
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  • 19. Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.
    McAnany JJ, Alexander KR, Kumar NM, Ying H, Anastasakis A, Fishman GA.
    Ophthalmic Genet; 2013 Sep; 34(3):167-73. PubMed ID: 23289809
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