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Journal Abstract Search

156 related items for PubMed ID: 14661912

  • 41. Undetectable S cone electroretinogram b-wave in complete congenital stationary night blindness.
    Kamiyama M, Yamamoto S, Nitta K, Hayasaka S.
    Br J Ophthalmol; 1996 Jul; 80(7):637-9. PubMed ID: 8795377
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  • 42. 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; 42(11):2728-36. PubMed ID: 11581222
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  • 43. [Electrophysiologic tests for diagnosis of congenital night blindness].
    Lubiński W, Palacz A, Penkala K, Palacz O.
    Klin Oczna; 1996 Jan; 98(1):9-12. PubMed ID: 9019583
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  • 44. 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 Jan; 10(9):e0137072. PubMed ID: 26368928
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  • 49. 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. PubMed ID: 2303327
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  • 50. Retinal on-pathway deficit in congenital disorder of glycosylation due to phosphomannomutase deficiency.
    Thompson DA, Lyons RJ, Liasis A, Russell-Eggitt I, Jägle H, Grünewald S.
    Arch Ophthalmol; 2012 Jun; 130(6):712-9. PubMed ID: 22801829
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  • 52. 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. PubMed ID: 9682699
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  • 53. 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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  • 55. 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. PubMed ID: 15845035
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  • 59. LED-generated multifocal ERG on- and off-responses in complete congenital stationary night blindness -- a case report.
    Leifert D, Todorova MG, Prünte C, Palmowski-Wolfe AM.
    Doc Ophthalmol; 2005 Jul; 111(1):1-6. PubMed ID: 16502301
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  • 60. Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
    Dinet V, Ciccotosto GD, Delaunay K, Borras C, Ranchon-Cole I, Kostic C, Savoldelli M, El Sanharawi M, Jonet L, Pirou C, An N, Abitbol M, Arsenijevic Y, Behar-Cohen F, Cappai R, Mascarelli F.
    Mol Brain; 2016 Jun 08; 9(1):64. PubMed ID: 27267879
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