-
1
-
-
0020535720
-
Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration
-
Gouras P, Eggers HM, MacKay CJ, (1983) Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration. Arch Ophthalmol 101: 718-724.
-
(1983)
Arch Ophthalmol
, vol.101
, pp. 718-724
-
-
Gouras, P.1
Eggers, H.M.2
MacKay, C.J.3
-
2
-
-
0021701259
-
Supernormal scotopic ERG in cone dystrophy
-
Alexander KR, Fishman GA, (1984) Supernormal scotopic ERG in cone dystrophy. Br J Ophthalmol 68: 69-78.
-
(1984)
Br J Ophthalmol
, vol.68
, pp. 69-78
-
-
Alexander, K.R.1
Fishman, G.A.2
-
3
-
-
51649151348
-
Cone dystrophy and supernormal dark-adapted b-waves in the electroretinogram
-
Foerster MH, Kellner U, Wessing A, (1990) Cone dystrophy and supernormal dark-adapted b-waves in the electroretinogram. Graefes Arch Clin Exp Ophthalmol 228: 116-119.
-
(1990)
Graefes Arch Clin Exp Ophthalmol
, vol.228
, pp. 116-119
-
-
Foerster, M.H.1
Kellner, U.2
Wessing, A.3
-
4
-
-
0029975887
-
Sites of disease action in a retinal dystrophy with supernormal and delayed rod electroretinogram b-waves
-
Hood DC, Cideciyan AV, Halevy DA, Jacobson SG, (1996) Sites of disease action in a retinal dystrophy with supernormal and delayed rod electroretinogram b-waves. Vision Res 36: 889-901.
-
(1996)
Vision Res
, vol.36
, pp. 889-901
-
-
Hood, D.C.1
Cideciyan, A.V.2
Halevy, D.A.3
Jacobson, S.G.4
-
5
-
-
0027449040
-
Cone dysfunction and supernormal scotopic electroretinogram with a high-intensity stimulus. A report of three cases
-
Kato M, Kobayashi R, Watanabe I, (1993) Cone dysfunction and supernormal scotopic electroretinogram with a high-intensity stimulus. A report of three cases. Doc Ophthalmol 84: 71-81.
-
(1993)
Doc Ophthalmol
, vol.84
, pp. 71-81
-
-
Kato, M.1
Kobayashi, R.2
Watanabe, I.3
-
6
-
-
14744271527
-
A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"
-
Michaelides M, Holder GE, Webster AR, Hunt DM, Bird AC, et al. (2005) A detailed phenotypic study of "cone dystrophy with supernormal rod ERG". Br J Ophthalmol 89: 332-339.
-
(2005)
Br J Ophthalmol
, vol.89
, pp. 332-339
-
-
Michaelides, M.1
Holder, G.E.2
Webster, A.R.3
Hunt, D.M.4
Bird, A.C.5
-
7
-
-
0027278986
-
Retinal cone dysfunction of supernormal rod ERG type. Five new cases
-
Rosenberg T, Simonsen SE, (1993) Retinal cone dysfunction of supernormal rod ERG type. Five new cases. Acta Ophthalmol (Copenh) 71: 246-255.
-
(1993)
Acta Ophthalmol (Copenh)
, vol.71
, pp. 246-255
-
-
Rosenberg, T.1
Simonsen, S.E.2
-
8
-
-
0025228039
-
Rod electroretinograms in an elevated cyclic guanosine monophosphate-type human retinal degeneration. Comparison with retinitis pigmentosa
-
Sandberg MA, Miller S, Berson EL, (1990) Rod electroretinograms in an elevated cyclic guanosine monophosphate-type human retinal degeneration. Comparison with retinitis pigmentosa. Invest Ophthalmol Vis Sci 31: 2283-2287.
-
(1990)
Invest Ophthalmol Vis Sci
, vol.31
, pp. 2283-2287
-
-
Sandberg, M.A.1
Miller, S.2
Berson, E.L.3
-
9
-
-
0022601061
-
Two cases of retinal degeneration with an unusual form of electroretinogram
-
Yagasaki K, Miyake Y, Litao RE, Ichikawa K, (1986) Two cases of retinal degeneration with an unusual form of electroretinogram. Doc Ophthalmol 63: 73-82.
-
(1986)
Doc Ophthalmol
, vol.63
, pp. 73-82
-
-
Yagasaki, K.1
Miyake, Y.2
Litao, R.E.3
Ichikawa, K.4
-
10
-
-
33748639936
-
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans
-
Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, et al. (2006) Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans. Am J Hum Genet 79: 574-579.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 574-579
-
-
Wu, H.1
Cowing, J.A.2
Michaelides, M.3
Wilkie, S.E.4
Jeffery, G.5
-
11
-
-
34548802405
-
Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes
-
Czirjak G, Toth ZE, Enyedi P, (2007) Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes. J Neurophysiol 98: 1213-1222.
-
(2007)
J Neurophysiol
, vol.98
, pp. 1213-1222
-
-
Czirjak, G.1
Toth, Z.E.2
Enyedi, P.3
-
12
-
-
0024761801
-
Characterization of a voltage-gated K+ channel that accelerates the rod response to dim light
-
Beech DJ, Barnes S, (1989) Characterization of a voltage-gated K+ channel that accelerates the rod response to dim light. Neuron 3: 573-581.
-
(1989)
Neuron
, vol.3
, pp. 573-581
-
-
Beech, D.J.1
Barnes, S.2
-
13
-
-
36749021268
-
Dynamic regulation of the voltage-gated Kv2.1 potassium channel by multisite phosphorylation
-
Mohapatra DP, Park KS, Trimmer JS, (2007) Dynamic regulation of the voltage-gated Kv2.1 potassium channel by multisite phosphorylation. Biochem Soc Trans 35: 1064-1068.
-
(2007)
Biochem Soc Trans
, vol.35
, pp. 1064-1068
-
-
Mohapatra, D.P.1
Park, K.S.2
Trimmer, J.S.3
-
14
-
-
43949131764
-
Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram
-
Ben Salah S, Kamei S, Senechal A, Lopez S, Bazalgette C, et al. (2008) Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram. Am J Ophthalmol 145: 1099-1106.
-
(2008)
Am J Ophthalmol
, vol.145
, pp. 1099-1106
-
-
Ben Salah, S.1
Kamei, S.2
Senechal, A.3
Lopez, S.4
Bazalgette, C.5
-
15
-
-
34848868115
-
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram
-
Thiagalingam S, McGee TL, Weleber RG, Sandberg MA, Trzupek KM, et al. (2007) Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram. Ophthalmic Genet 28: 135-142.
-
(2007)
Ophthalmic Genet
, vol.28
, pp. 135-142
-
-
Thiagalingam, S.1
McGee, T.L.2
Weleber, R.G.3
Sandberg, M.A.4
Trzupek, K.M.5
-
16
-
-
40649085627
-
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2
-
Wissinger B, Dangel S, Jagle H, Hansen L, Baumann B, et al. (2008) Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2. Invest Ophthalmol Vis Sci 49: 751-757.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 751-757
-
-
Wissinger, B.1
Dangel, S.2
Jagle, H.3
Hansen, L.4
Baumann, B.5
-
17
-
-
75149182350
-
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
-
Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, et al. (2010) "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology. Retina 30: 51-62.
-
(2010)
Retina
, vol.30
, pp. 51-62
-
-
Robson, A.G.1
Webster, A.R.2
Michaelides, M.3
Downes, S.M.4
Cowing, J.A.5
-
18
-
-
84856030990
-
High-resolution optical coherence tomography imaging in KCNV2 retinopathy
-
Sergouniotis PI, Holder GE, Robson AG, Michaelides M, Webster AR, et al. (2012) High-resolution optical coherence tomography imaging in KCNV2 retinopathy. Br J Ophthalmol 96: 213-217.
-
(2012)
Br J Ophthalmol
, vol.96
, pp. 213-217
-
-
Sergouniotis, P.I.1
Holder, G.E.2
Robson, A.G.3
Michaelides, M.4
Webster, A.R.5
-
19
-
-
81255152054
-
Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response
-
Wissinger B, Schaich S, Baumann B, Bonin M, Jägle H, et al. (2011) Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. Hum Mutat 32: 1398-1406.
-
(2011)
Hum Mutat
, vol.32
, pp. 1398-1406
-
-
Wissinger, B.1
Schaich, S.2
Baumann, B.3
Bonin, M.4
Jägle, H.5
-
20
-
-
38649123067
-
ISCEV guidelines for clinical multifocal electroretinography (2007 edition)
-
Hood DC, Bach M, Brigell M, Keating D, Kondo M, et al. (2008) ISCEV guidelines for clinical multifocal electroretinography (2007 edition). Doc Ophthalmol 116: 1-11.
-
(2008)
Doc Ophthalmol
, vol.116
, pp. 1-11
-
-
Hood, D.C.1
Bach, M.2
Brigell, M.3
Keating, D.4
Kondo, M.5
-
21
-
-
59049100882
-
ISCEV Standard for full-field clinical electroretinography (2008 update)
-
Marmor MF, Fulton AB, Holder GE, Miyake Y, Brigell M, et al. (2009) ISCEV Standard for full-field clinical electroretinography (2008 update). Doc Ophthalmol 118: 69-77.
-
(2009)
Doc Ophthalmol
, vol.118
, pp. 69-77
-
-
Marmor, M.F.1
Fulton, A.B.2
Holder, G.E.3
Miyake, Y.4
Brigell, M.5
-
22
-
-
0027490062
-
Comparison of three methods of estimating the parameters of the Naka-Rushton equation
-
Evans LS, Peachey NS, Marchese AL, (1993) Comparison of three methods of estimating the parameters of the Naka-Rushton equation. Doc Ophthalmol 84: 19-30.
-
(1993)
Doc Ophthalmol
, vol.84
, pp. 19-30
-
-
Evans, L.S.1
Peachey, N.S.2
Marchese, A.L.3
-
23
-
-
0028229520
-
Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave
-
Hood DC, Birch DG, (1994) Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave. Invest Ophthalmol Vis Sci 35: 2948-2961.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 2948-2961
-
-
Hood, D.C.1
Birch, D.G.2
-
24
-
-
84860269433
-
Assessment of "non-recordable" electroretinograms by 9 Hz flicker stimulation under scotopic conditions
-
Schatz A, Wilke R, Strasser T, Gekeler F, Messias A, et al. (2012) Assessment of "non-recordable" electroretinograms by 9 Hz flicker stimulation under scotopic conditions. Doc Ophthalmol 124: 27-39.
-
(2012)
Doc Ophthalmol
, vol.124
, pp. 27-39
-
-
Schatz, A.1
Wilke, R.2
Strasser, T.3
Gekeler, F.4
Messias, A.5
-
25
-
-
0032402112
-
Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities
-
Sharpe LT, Stockman A, Jägle H, Knau H, Klausen G, et al. (1998) Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities. J Neurosci 18: 10053-10069.
-
(1998)
J Neurosci
, vol.18
, pp. 10053-10069
-
-
Sharpe, L.T.1
Stockman, A.2
Jägle, H.3
Knau, H.4
Klausen, G.5
-
26
-
-
0024615782
-
The genes for color vision
-
Nathans J, (1989) The genes for color vision. Sci Am 260: 42-49.
-
(1989)
Sci Am
, vol.260
, pp. 42-49
-
-
Nathans, J.1
-
27
-
-
84855411632
-
Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2
-
Friedburg C, Wissinger B, Schambeck M, Bonin M, Kohl S, et al. (2011) Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2. Invest Ophthalmol Vis Sci 52: 8621-8629.
-
(2011)
Invest Ophthalmol Vis Sci
, vol.52
, pp. 8621-8629
-
-
Friedburg, C.1
Wissinger, B.2
Schambeck, M.3
Bonin, M.4
Kohl, S.5
-
28
-
-
0028047341
-
After Transduction: Response Shaping and Control of Transmission by Ion Channels of the Photoreceptor Inner Segment
-
Barnes S, (1994) After Transduction: Response Shaping and Control of Transmission by Ion Channels of the Photoreceptor Inner Segment. Neurosci 58: 447-459.
-
(1994)
Neurosci
, vol.58
, pp. 447-459
-
-
Barnes, S.1
-
29
-
-
28844452863
-
PIII and derived PII analysis in a patient with retinal dysfunction with supernormal scotopic ERG
-
Tanimoto N, Usui T, Ichibe M, Takagi M, Hasegawa S, et al. (2005) PIII and derived PII analysis in a patient with retinal dysfunction with supernormal scotopic ERG. Doc Ophthalmol 110: 219-226.
-
(2005)
Doc Ophthalmol
, vol.110
, pp. 219-226
-
-
Tanimoto, N.1
Usui, T.2
Ichibe, M.3
Takagi, M.4
Hasegawa, S.5
-
31
-
-
12344263806
-
Cone function studied with flicker electroretinogram during progressive retinal degeneration in RCS rats
-
Pinilla I, Lund RD, Sauve Y, (2005) Cone function studied with flicker electroretinogram during progressive retinal degeneration in RCS rats. Exp Eye Res 80: 51-59.
-
(2005)
Exp Eye Res
, vol.80
, pp. 51-59
-
-
Pinilla, I.1
Lund, R.D.2
Sauve, Y.3
-
32
-
-
79953143745
-
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome
-
Thompson DA, Feather S, Stanescu HC, Freudenthal B, Zdebik AA, et al. (2011) Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. J Physiol 589: 1681-1689.
-
(2011)
J Physiol
, vol.589
, pp. 1681-1689
-
-
Thompson, D.A.1
Feather, S.2
Stanescu, H.C.3
Freudenthal, B.4
Zdebik, A.A.5
-
33
-
-
0034255132
-
Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina
-
Kofuji P, Ceelen P, Zahs KR, Surbeck LW, Lester HA, et al. (2000) Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina. J Neurosci 20: 5733-5740.
-
(2000)
J Neurosci
, vol.20
, pp. 5733-5740
-
-
Kofuji, P.1
Ceelen, P.2
Zahs, K.R.3
Surbeck, L.W.4
Lester, H.A.5
|