-
1
-
-
0024538020
-
Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa
-
Flannery JG, Farber DB, Bird AC, Bok D. Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci 1989;30:191-211.
-
(1989)
Invest Ophthalmol Vis Sci
, vol.30
, pp. 191-211
-
-
Flannery, J.G.1
Farber, D.B.2
Bird, A.C.3
Bok, D.4
-
4
-
-
0021948505
-
Retinal histopathology of a carrier of X-chromosome-linked retinitis pigmentosa
-
Szamier RB, Berson EL. Retinal histopathology of a carrier of X-chromosome-linked retinitis pigmentosa. Ophthalmology 1985;92:271-8.
-
(1985)
Ophthalmology
, vol.92
, pp. 271-278
-
-
Szamier, R.B.1
Berson, E.L.2
-
5
-
-
0026460822
-
Morphometric analysis of macular photoreceptors and ganglion cells in retinas with retinitis pigmentosa
-
Stone JL, Barlow WE, Humayun MS, et al. Morphometric analysis of macular photoreceptors and ganglion cells in retinas with retinitis pigmentosa. Arch Ophthalmol 1992;110: 1634-9.
-
(1992)
Arch Ophthalmol
, vol.110
, pp. 1634-1639
-
-
Stone, J.L.1
Barlow, W.E.2
Humayun, M.S.3
-
6
-
-
0029740915
-
Clinical and histopathologic findings in clumped pigmentary retinal degeneration
-
To KW, Adamian M, Jakobiec FA, Berson EL. Clinical and histopathologic findings in clumped pigmentary retinal degeneration. Arch Ophthalmol 1996;114:950-5.
-
(1996)
Arch Ophthalmol
, vol.114
, pp. 950-955
-
-
To, K.W.1
Adamian, M.2
Jakobiec, F.A.3
Berson, E.L.4
-
8
-
-
0023037646
-
Cone-rod dystrophy. A clinical and histopathologic report
-
Rabb MF, Tso MOM, Fishman GA. Cone-rod dystrophy. A clinical and histopathologic report. Ophthalmology 1986;93: 1443-51.
-
(1986)
Ophthalmology
, vol.93
, pp. 1443-1451
-
-
Rabb, M.F.1
Tso, M.O.M.2
Fishman, G.A.3
-
9
-
-
0027982045
-
Histopathology and immunocytochemistry of the neurosensory retina in fundus flavimaculatus
-
Birnbach CD, Järveläinen M, Possin DE, Milam AH. Histopathology and immunocytochemistry of the neurosensory retina in fundus flavimaculatus. Ophthalmology 1994;101: 1211-9.
-
(1994)
Ophthalmology
, vol.101
, pp. 1211-1219
-
-
Birnbach, C.D.1
Järveläinen, M.2
Possin, D.E.3
Milam, A.H.4
-
11
-
-
0028233212
-
Clinicopathologic correlation of drusen and retinal pigment epithelial abnormalities in age-related macular degeneration
-
Bressler NM, Silva JC, Bressler SB, et al. Clinicopathologic correlation of drusen and retinal pigment epithelial abnormalities in age-related macular degeneration. Retina 1994;14: 130-42.
-
(1994)
Retina
, vol.14
, pp. 130-142
-
-
Bressler, N.M.1
Silva, J.C.2
Bressler, S.B.3
-
12
-
-
0027452693
-
Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation
-
To KW, Adamian M, Jakobiec FA, Berson EL. Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation. Ophthalmology 1993;100:15-23.
-
(1993)
Ophthalmology
, vol.100
, pp. 15-23
-
-
To, K.W.1
Adamian, M.2
Jakobiec, F.A.3
Berson, E.L.4
-
13
-
-
0031908931
-
Histopathologic and immunohistochemical study of an autopsy eye with X-linked cone degeneration
-
To KW, Adamian M, Jakobiec FA, Berson EL. Histopathologic and immunohistochemical study of an autopsy eye with X-linked cone degeneration. Arch Ophthalmol 1998; 116:100-3.
-
(1998)
Arch Ophthalmol
, vol.116
, pp. 100-103
-
-
To, K.W.1
Adamian, M.2
Jakobiec, F.A.3
Berson, E.L.4
-
15
-
-
0027434085
-
Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS gene
-
Weleber RG, Carr RE, Murphey WH, et al. Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS gene. Arch Ophthalmol 1993;111:1531-42.
-
(1993)
Arch Ophthalmol
, vol.111
, pp. 1531-1542
-
-
Weleber, R.G.1
Carr, R.E.2
Murphey, W.H.3
-
16
-
-
0028804575
-
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration
-
Gorin MB, Jackson KE, Ferrell RE, et al. A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. Ophthalmology 1995;102:246-55.
-
(1995)
Ophthalmology
, vol.102
, pp. 246-255
-
-
Gorin, M.B.1
Jackson, K.E.2
Ferrell, R.E.3
-
17
-
-
0027447531
-
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
-
Wells J, Wroblewski J, Keen J, et al. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet 1993;3:213-8.
-
(1993)
Nat Genet
, vol.3
, pp. 213-218
-
-
Wells, J.1
Wroblewski, J.2
Keen, J.3
-
18
-
-
0031019503
-
Serine-27 - Phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophy
-
Fishman GA, Stone EM, Alexander KR, et al. Serine-27 - phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophy. Ophthalmology 1997;104:299-306.
-
(1997)
Ophthalmology
, vol.104
, pp. 299-306
-
-
Fishman, G.A.1
Stone, E.M.2
Alexander, K.R.3
-
19
-
-
0030669568
-
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
-
Freund CL, Gregory-Evans CY, Furukawa T, et al. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell 1997;91:543-53.
-
(1997)
Cell
, vol.91
, pp. 543-553
-
-
Freund, C.L.1
Gregory-Evans, C.Y.2
Furukawa, T.3
-
20
-
-
0030725687
-
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
-
Furukawa T, Morrow EM, Cepko CL. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell 1997;91: 531-41.
-
(1997)
Cell
, vol.91
, pp. 531-541
-
-
Furukawa, T.1
Morrow, E.M.2
Cepko, C.L.3
-
21
-
-
0031447030
-
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration
-
Swain PK, Chen S, Wang QL, et al. Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. Neuron 1997;19:1329-36.
-
(1997)
Neuron
, vol.19
, pp. 1329-1336
-
-
Swain, P.K.1
Chen, S.2
Wang, Q.L.3
-
22
-
-
0030894570
-
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p
-
Kelsell RE, Evans K, Gregory CY, et al. Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p. Hum Mol Genet 1997;6:597-600.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 597-600
-
-
Kelsell, R.E.1
Evans, K.2
Gregory, C.Y.3
-
23
-
-
0025269578
-
Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxia
-
Hamilton SR, Chatrian GE, Mills RP, et al. Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxia. Arch Ophthalmol 1990;108:551-6.
-
(1990)
Arch Ophthalmol
, vol.108
, pp. 551-556
-
-
Hamilton, S.R.1
Chatrian, G.E.2
Mills, R.P.3
-
24
-
-
0027323737
-
Cone dystrophies with negative photopic electroretinogram
-
Kellner U, Foerster MH. Cone dystrophies with negative photopic electroretinogram. Br J Ophthalmol 1993;77:404-9.
-
(1993)
Br J Ophthalmol
, vol.77
, pp. 404-409
-
-
Kellner, U.1
Foerster, M.H.2
-
25
-
-
0027604342
-
Pattern of dysfunction in progressive cone dystrophies - An extended classification
-
Kellner U, Foerster MH. Pattern of dysfunction in progressive cone dystrophies - an extended classification. Ger J Ophthalmol 1993;2:170-7.
-
(1993)
Ger J Ophthalmol
, vol.2
, pp. 170-177
-
-
Kellner, U.1
Foerster, M.H.2
-
26
-
-
0031980355
-
Rhodopsin transgenic pigs as a model for human retinitis pigmentosa
-
Li ZY, Wong F, Chang JH, et al. Rhodopsin transgenic pigs as a model for human retinitis pigmentosa. Invest Ophthalmol Vis Sci 1998;39:808-19.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, pp. 808-819
-
-
Li, Z.Y.1
Wong, F.2
Chang, J.H.3
-
27
-
-
0030669676
-
A pathologic study of degeneration of the rod and cone populations of the rhodopsin Pro347Leu transgenic pigs
-
Tso MOM, Li WW, Zhang C, et al. A pathologic study of degeneration of the rod and cone populations of the rhodopsin Pro347Leu transgenic pigs. Trans Am Ophthalmol Soc 1997; 95:467-79.
-
(1997)
Trans Am Ophthalmol Soc
, vol.95
, pp. 467-479
-
-
Tso, M.O.M.1
Li, W.W.2
Zhang, C.3
-
28
-
-
0030851707
-
Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa
-
Petters RM, Alexander CA, Wells KD, et al. Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa. Nat Biotechnol 1997;15:965-70.
-
(1997)
Nat Biotechnol
, vol.15
, pp. 965-970
-
-
Petters, R.M.1
Alexander, C.A.2
Wells, K.D.3
-
29
-
-
0003098244
-
Apoptosis in retinitis pigmentosa
-
Anderson RE, Hollyfield JG, LaVail MM, eds. New York, NY: Plenum Press
-
Li Z-Y, Milam AH. Apoptosis in retinitis pigmentosa. In: Anderson RE, Hollyfield JG, LaVail MM, eds. Retinal Degeneration II. New York, NY: Plenum Press, 1995; 1-12.
-
(1995)
Retinal Degeneration II
, pp. 1-12
-
-
Li, Z.-Y.1
Milam, A.H.2
|