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Journal Abstract Search

310 related items for PubMed ID: 26246500

  • 21.
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  • 22. Congenital Stationary Night Blindness.
    Tsang SH, Sharma T.
    Adv Exp Med Biol; 2018; 1085():61-64. PubMed ID: 30578486
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  • 26. Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient.
    Lee YJ, Joo K, Seong MW, Park KH, Park SS, Woo SJ.
    Korean J Ophthalmol; 2020 Apr; 34(2):170-172. PubMed ID: 32233153
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  • 28. Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.
    Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE.
    Hum Mol Genet; 2015 Nov 01; 24(21):6229-39. PubMed ID: 26310623
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  • 29. Signal sequence cleavage and plasma membrane targeting of the retinal rod NCKX1 and cone NCKX2 Na+/Ca2+ - K+ exchangers.
    Kang K, Schnetkamp PP.
    Biochemistry; 2003 Aug 12; 42(31):9438-45. PubMed ID: 12899631
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  • 33. Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.
    Miraldi Utz V, Pfeifer W, Longmuir SQ, Olson RJ, Wang K, Drack AV.
    JAMA Ophthalmol; 2018 Apr 01; 136(4):389-398. PubMed ID: 29522070
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  • 34. Clinical characterisation of the CABP4-related retinal phenotype.
    Khan AO, Alrashed M, Alkuraya FS.
    Br J Ophthalmol; 2013 Mar 01; 97(3):262-5. PubMed ID: 23099293
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  • 35. Zebrafish Cacna1fa is required for cone photoreceptor function and synaptic ribbon formation.
    Jia S, Muto A, Orisme W, Henson HE, Parupalli C, Ju B, Baier H, Taylor MR.
    Hum Mol Genet; 2014 Jun 01; 23(11):2981-94. PubMed ID: 24419318
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  • 36. Macular sensitivity in patients with congenital stationary night-blindness.
    William A, Kohl S, Zeitz C, Willmann G, Zrenner E, Bartz-Schmidt KU, Gekeler F, Schatz A.
    Br J Ophthalmol; 2019 Oct 01; 103(10):1507-1510. PubMed ID: 30573500
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  • 37. Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms.
    Zeitz C, Robson AG, Audo I.
    Prog Retin Eye Res; 2015 Mar 01; 45():58-110. PubMed ID: 25307992
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  • 38. Assembly of retinal rod or cone Na(+)/Ca(2+)-K(+) exchanger oligomers with cGMP-gated channel subunits as probed with heterologously expressed cDNAs.
    Kang K, Bauer PJ, Kinjo TG, Szerencsei RT, Bönigk W, Winkfein RJ, Schnetkamp PP.
    Biochemistry; 2003 Apr 22; 42(15):4593-600. PubMed ID: 12693957
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  • 40. 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 22; 257(6):1207-1215. PubMed ID: 30982101
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