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183 related items for PubMed ID: 3498069
41. Gradient of deficit in cone responses in the incomplete form of congenital stationary night blindness revealed by multifocal electroretinography. Tremblay F, Parkinson J. Doc Ophthalmol; 2008 Jan; 116(1):41-7. PubMed ID: 17721714 [Abstract] [Full Text] [Related]
42. 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; 29(6):274-9. PubMed ID: 7834566 [Abstract] [Full Text] [Related]
43. 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 [Abstract] [Full Text] [Related]
44. Photopic abnormalities in congenital stationary nightblindness. Krill AE, Martin D. Invest Ophthalmol; 1971 Aug 15; 10(8):625-36. PubMed ID: 5315207 [No Abstract] [Full Text] [Related]
45. 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 15; 111(1):15-21. PubMed ID: 16502303 [Abstract] [Full Text] [Related]
46. [Electrophysiologic tests for diagnosis of congenital night blindness]. Lubiński W, Palacz A, Penkala K, Palacz O. Klin Oczna; 1996 Jan 15; 98(1):9-12. PubMed ID: 9019583 [Abstract] [Full Text] [Related]
47. ERG characteristics of congenital stationary night blindness. Wu D, Xu X, Wu L, Luo T. Yan Ke Xue Bao; 1990 Jun 15; 6(1-2):32-5. PubMed ID: 2101357 [Abstract] [Full Text] [Related]
48. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, Bergen AA, Prinsen CF, Polomeno RC, Gal A, Drack AV, Musarella MA, Jacobson SG, Young RS, Weleber RG. Nat Genet; 2000 Nov 15; 26(3):319-23. PubMed ID: 11062471 [Abstract] [Full Text] [Related]
49. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Bech-Hansen NT, Naylor MJ, Maybaum TA, Pearce WG, Koop B, Fishman GA, Mets M, Musarella MA, Boycott KM. Nat Genet; 1998 Jul 15; 19(3):264-7. PubMed ID: 9662400 [Abstract] [Full Text] [Related]
50. Recording multifocal electroretinogram on and off responses in humans. Kondo M, Miyake Y, Horiguchi M, Suzuki S, Tanikawa A. Invest Ophthalmol Vis Sci; 1998 Mar 15; 39(3):574-80. PubMed ID: 9501869 [Abstract] [Full Text] [Related]
51. Modulation of the human photopic ERG luminance-response function with the use of chromatic stimuli. Rufiange M, Dumont M, Lachapelle P. Vision Res; 2005 Aug 15; 45(17):2321-30. PubMed ID: 15924945 [Abstract] [Full Text] [Related]
52. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder. Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI. Invest Ophthalmol Vis Sci; 2009 May 15; 50(5):2344-50. PubMed ID: 19074807 [Abstract] [Full Text] [Related]
53. Phenotypic variation in enhanced S-cone syndrome. Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE. Invest Ophthalmol Vis Sci; 2008 May 15; 49(5):2082-93. PubMed ID: 18436841 [Abstract] [Full Text] [Related]
54. Ring analysis of multifocal oscillatory potentials (mfOPs) in cCSNB suggests near-normal ON-OFF pathways at the fovea only. Dorfman AL, Gauvin M, Vatcher D, Little JM, Polomeno RC, Lachapelle P. Doc Ophthalmol; 2020 Oct 15; 141(2):99-109. PubMed ID: 32060756 [Abstract] [Full Text] [Related]
55. Large rod-like photopic signals in a possible new form of congenital night blindness. Marmor MF. Doc Ophthalmol; 1989 Mar 15; 71(3):265-9. PubMed ID: 2789128 [Abstract] [Full Text] [Related]
56. Unique characteristics of two types of retinitis pigmentosa patients with different rod sensitivities. Takahashi H, Miyake Y, Horiguchi M, Tomida N, Takakuwa H. Jpn J Ophthalmol; 2005 Mar 15; 49(2):114-20. PubMed ID: 15838727 [Abstract] [Full Text] [Related]
57. Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex. Sandmeyer LS, Breaux CB, Archer S, Grahn BH. Vet Ophthalmol; 2007 Mar 15; 10(6):368-75. PubMed ID: 17970998 [Abstract] [Full Text] [Related]
58. [Congenital stationary night blindness]. Kocyła-Karczmarewicz B, Grałek M, Juszko J, Trzebicka A, Sarti G. Klin Oczna; 2004 Mar 15; 106(3 Suppl):509-11. PubMed ID: 15636252 [Abstract] [Full Text] [Related]
59. Incomplete congenital stationary night blindness: electroretinogram c-wave and electrooculogram light rise. Takahashi Y, Onoe S, Asamizu N, Mori T, Yoshimura Y, Tazawa Y. Doc Ophthalmol; 1988 Sep 15; 70(1):67-75. PubMed ID: 3265910 [Abstract] [Full Text] [Related]
60. 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 15; 111(1):1-6. PubMed ID: 16502301 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]