174 related articles for article (PubMed ID: 6607068)
21. Progressive cone dystrophies.
François J; De Rouck A; De Laey JJ
Ophthalmologica; 1976; 173(2):81-101. PubMed ID: 1066593
[TBL] [Abstract][Full Text] [Related]
22. Natural history and biomarkers of KCNV2-associated retinopathy.
Sakti DH; Cornish EE; Ali H; Retsas S; Raza M; Saakova N; Carvalho LS; Nash BM; Jamieson RV; Grigg JR
Clin Exp Ophthalmol; 2024 Jul; 52(5):528-544. PubMed ID: 38443311
[TBL] [Abstract][Full Text] [Related]
23. Retinal cone dysfunction of supernormal rod ERG type. Five new cases.
Rosenberg T; Simonsen SE
Acta Ophthalmol (Copenh); 1993 Apr; 71(2):246-55. PubMed ID: 8333273
[TBL] [Abstract][Full Text] [Related]
24. 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
[TBL] [Abstract][Full Text] [Related]
25. H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.
Valleix S; Nedelec B; Rigaudiere F; Dighiero P; Pouliquen Y; Renard G; Le Gargasson JF; Delpech M
Invest Ophthalmol Vis Sci; 2006 Jan; 47(1):48-54. PubMed ID: 16384943
[TBL] [Abstract][Full Text] [Related]
26. 'On' response defect in paraneoplastic night blindness with cutaneous malignant melanoma.
Alexander KR; Fishman GA; Peachey NS; Marchese AL; Tso MO
Invest Ophthalmol Vis Sci; 1992 Mar; 33(3):477-83. PubMed ID: 1544774
[TBL] [Abstract][Full Text] [Related]
27. Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.
Kabanarou SA; Holder GE; Fitzke FW; Bird AC; Webster AR
Br J Ophthalmol; 2004 Aug; 88(8):1018-22. PubMed ID: 15258017
[TBL] [Abstract][Full Text] [Related]
28. Cone dysfunction and supernormal scotopic electroretinogram with a high-intensity stimulus. A report of three cases.
Kato M; Kobayashi R; Watanabe I
Doc Ophthalmol; 1993; 84(1):71-81. PubMed ID: 8223112
[TBL] [Abstract][Full Text] [Related]
29. Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy).
Haimovici R; Wroblewski J; Piguet B; Fitzke FW; Holder GE; Arden GB; Bird AC
Eye (Lond); 2002 Jan; 16(1):7-15. PubMed ID: 11913893
[TBL] [Abstract][Full Text] [Related]
30. ERG rod a-wave in Oguchi disease.
Usui T; Tanimoto N; Ueki S; Takagi M; Hasegawa S; Abe H; Sekiya K; Nakazawa M
Vision Res; 2004 Mar; 44(5):535-40. PubMed ID: 14680778
[TBL] [Abstract][Full Text] [Related]
31. Fundus albipunctatus associated with cone dystrophy.
Miyake Y; Shiroyama N; Sugita S; Horiguchi M; Yagasaki K
Br J Ophthalmol; 1992 Jun; 76(6):375-9. PubMed ID: 1622952
[TBL] [Abstract][Full Text] [Related]
32. Rod-cone dystrophy associated with a rod system electroretinogram obtained under photopic conditions.
Fishman GA; Peachey NS
Ophthalmology; 1989 Jun; 96(6):913-8. PubMed ID: 2787013
[TBL] [Abstract][Full Text] [Related]
33. 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
[TBL] [Abstract][Full Text] [Related]
34. Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutation.
Khan AO; Aldahmesh MA; Abu-Safieh L; Alkuraya FS
Ophthalmic Genet; 2014 Sep; 35(3):130-7. PubMed ID: 23767994
[TBL] [Abstract][Full Text] [Related]
35. Color electroretinography. A method for separation of dysfunctions of cones.
Kellner U; Foerster MH
Doc Ophthalmol; 1992; 80(1):13-23. PubMed ID: 1505335
[TBL] [Abstract][Full Text] [Related]
36. Application of visually evoked response near the threshold of vision to objective measurement of dark adaptation.
Fujimura K; Tsuchida Y; Morita Y; Jacobson JH
Am J Ophthalmol; 1975 Jan; 79(1):141-50. PubMed ID: 1078571
[TBL] [Abstract][Full Text] [Related]
37. [Multi-flash ERG in cone dystrophies and cone-rod dystrophies].
Walter P; Widder RA; Brunner R
Klin Monbl Augenheilkd; 1998 Feb; 212(2):88-92. PubMed ID: 9577807
[TBL] [Abstract][Full Text] [Related]
38. Blood-retinal barrier function in patients with cone or cone-rod dystrophy.
Fishman GA; Rhee AJ; Blair NP
Arch Ophthalmol; 1986 Apr; 104(4):545-8. PubMed ID: 3954658
[TBL] [Abstract][Full Text] [Related]
39. The effect of age on human cone and rod ganzfeld electroretinograms.
Weleber RG
Invest Ophthalmol Vis Sci; 1981 Mar; 20(3):392-9. PubMed ID: 7203883
[TBL] [Abstract][Full Text] [Related]
40. Electrophysiological findings in persons with nyctalopia.
Chia A; Luu CD
Ann Acad Med Singap; 2006 Dec; 35(12):864-7. PubMed ID: 17218997
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]