-
1
-
-
0003520592
-
Statistics on blindness in the model reporting area 1969-70
-
United States Department of Health. Education and Welfare, Washington, DC.
-
(1973)
-
-
Kahn, H.A.1
Moorhead, H.B.2
-
3
-
-
0019020390
-
The Framingham Eye Study monograph: An ophthalmological and epidemiological study of cataract, glaucoma, diabetic retinopathy, macular degeneration, and visual acuity in a general population of 2631 adults, 1973-1975
-
(1980)
Surv. Ophthalmol.
, vol.24
, pp. 335-610
-
-
Leibowitz, H.M.1
Krueger, D.E.2
Maunder, L.R.3
Milton, R.C.4
Kini, M.M.5
Kahn, H.A.6
Nickerson, R.J.7
Pool, J.8
Colton, T.L.9
Ganley, J.P.10
Loewenstein, J.I.11
Dawber, T.R.12
-
5
-
-
0028934221
-
An international classification and grading system for age-related maculopathy and age-related macular degeneration
-
The International ARM Epidemiological Study Group.
-
(1995)
Surv. Ophthalmol.
, vol.39
, pp. 367-374
-
-
Bird, A.C.1
Bressler, N.M.2
Bressler, S.B.3
Chisholm, I.H.4
Coscas, G.5
Davis, M.D.6
De Jong, P.T.7
Klaver, C.C.8
Klein, B.E.9
Klein, R.10
-
22
-
-
0025721075
-
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa
-
(1991)
Nature
, vol.354
, pp. 478-480
-
-
Farrar, G.J.1
Kenna, P.2
Jordan, S.A.3
Kumar-Singh, R.4
Humphries, M.M.5
Sharp, E.M.6
Sheils, D.M.7
Humphries, P.8
-
24
-
-
0027447531
-
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
-
(1993)
Nat. Genet.
, vol.3
, pp. 213-218
-
-
Wells, J.1
Wroblewski, J.2
Keen, J.3
Inglehearn, C.4
Jubb, C.5
Eckstein, A.6
Jay, M.7
Arden, G.8
Bhattacharya, S.9
Fitzke, F.10
-
30
-
-
0026662677
-
The gene for Best's macular dystrophy is located at 11q13 in a Swedish family
-
(1992)
Clin. Genet.
, vol.42
, pp. 156-159
-
-
Forsman, K.1
Graff, C.2
Nordstrom, S.3
Johansson, K.4
Westermark, E.5
Lundgren, E.6
Gustavson, K.H.7
Wadelius, C.8
Holmgren, G.9
-
31
-
-
17344364275
-
Identification of the gene responsible for Best macular dystrophy
-
(1998)
Nat. Genet.
, vol.19
, pp. 241-247
-
-
Petrukhin, K.1
Koisti, M.J.2
Bakall, B.3
Li, W.4
Xie, G.5
Marknell, T.6
Sandgren, O.7
Forsman, K.8
Holmgren, G.9
Andreasson, S.10
-
32
-
-
0033739625
-
Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 12758-12763
-
-
Marmorstein, A.D.1
Marmorstein, L.Y.2
Rayborn, M.3
Wang, X.4
Hollyfield, J.G.5
Petrukhin, K.6
-
33
-
-
20244378502
-
Allelic variation in the VMD2 gene in best disease and age-related macular degeneration
-
(2000)
Invest. Ophthalmol. Vis. Sci.
, vol.41
, pp. 1291-1296
-
-
Lotery, A.J.1
Munier, F.L.2
Fishman, G.A.3
Weleber, R.G.4
Jacobson, S.G.5
Affatigato, L.M.6
Nichols, B.E.7
Schorderet, D.F.8
Sheffield, V.C.9
Stone, E.M.10
-
34
-
-
0027372405
-
A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1
-
(1993)
Nat. Genet.
, vol.5
, pp. 308-311
-
-
Kaplan, J.1
Gerber, S.2
Larget-Piet, D.3
Rozet, J.M.4
Dollfus, H.5
Dufier, J.L.6
Odent, S.7
Postel-Vinay, A.8
Janin, N.9
Briard, M.L.10
-
35
-
-
0031037951
-
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
-
(1997)
Nat. Genet.
, vol.15
, pp. 236-246
-
-
Allikmets, R.1
Singh, N.2
Sun, H.3
Shroyer, N.F.4
Hutchinson, A.5
Chidambaram, A.6
Gerrard, B.7
Baird, L.8
Stauffer, D.9
Peiffer, A.10
-
37
-
-
0000761427
-
Retinal stimulates ATP hydrolysis by purified and reconstituted ABCR, the photoreceptor-specific ATP-binding cassette transporter responsible for Stargardt disease
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 8269-8281
-
-
Sun, H.1
Molday, R.S.2
Nathans, J.3
-
40
-
-
0034671726
-
Age-related macular degeneration. The lipofusion component N-retinyl-N-retinylidene ethanolamine detaches proapoptotic proteins from mitochondria and induces apoptosis in mammalian retinal pigment epithelial cells
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 39625-39630
-
-
Suter, M.1
Reme, C.2
Grimm, C.3
Wenzel, A.4
Jaattela, M.5
Esser, P.6
Kociok, N.7
Leist, M.8
Richter, C.9
-
44
-
-
0012119330
-
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration
-
(1997)
Science
, vol.277
, pp. 1805-1807
-
-
Allikmets, R.1
Shroyer, N.F.2
Singh, N.3
Seddon, J.M.4
Lewis, R.A.5
Bernstein, P.S.6
Peiffer, A.7
Zabriskie, N.A.8
Li, Y.9
Hutchinson, A.10
-
45
-
-
0033859128
-
Further evidence for an association of ABCR alleles with age-related macular degeneration
-
The International ABCR Screening Consortium
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 487-491
-
-
Allikmets, R.1
-
47
-
-
0035024249
-
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degeneration
-
(2001)
Arch. Ophthalmol.
, vol.119
, pp. 745-751
-
-
Guymer, R.H.1
Heon, E.2
Lotery, A.J.3
Munier, F.L.4
Schorderet, D.F.5
Baird, P.N.6
McNeil, R.J.7
Haines, H.8
Sheffield, V.C.9
Stone, E.M.10
-
48
-
-
0035032384
-
An analysis of allelic variation in the ABCA4 gene
-
(2001)
Invest. Ophthalmol. Vis. Sci.
, vol.42
, pp. 1179-1189
-
-
Webster, A.R.1
Heon, E.2
Lotery, A.J.3
Vandenburgh, K.4
Casavant, T.L.5
Oh, K.T.6
Beck, G.7
Fishman, G.A.8
Lam, B.L.9
Levin, A.10
-
54
-
-
0000748599
-
A pathological report upon a casae of Doyne's choroiditis ('honeycomb' or 'family choroiditis')
-
(1913)
Ophthalmoscope
, vol.11
, pp. 537-538
-
-
Collins, T.1
-
55
-
-
9044250844
-
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21
-
(1996)
Arch. Ophthalmol.
, vol.114
, pp. 193-198
-
-
Heon, E.1
Piguet, B.2
Munier, F.3
Sneed, S.R.4
Morgan, C.M.5
Forni, S.6
Pescia, G.7
Schorderet, D.8
Taylor, C.M.9
Streb, L.M.10
Wiles, C.D.11
Nishimura, D.Y.12
Sheffield, V.C.13
Stone, E.M.14
-
56
-
-
0033027071
-
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy
-
(1999)
Nat. Genet.
, vol.22
, pp. 199-202
-
-
Stone, E.M.1
Lotery, A.J.2
Munier, F.L.3
Heon, E.4
Piguet, B.5
Guymer, R.H.6
Vandenburgh, K.7
Cousin, P.8
Nishimura, D.9
Swiderski, R.E.10
-
59
-
-
0035069172
-
Autosomal dominant Stargardt-like macular dystrophy: Founder effect and reassessment of genetic heterogeneity
-
(2001)
Arch. Ophthalmol.
, vol.119
, pp. 564-570
-
-
Donoso, L.A.1
Frost, A.T.2
Stone, E.M.3
Weleber, R.G.4
MacDonald, I.M.5
Hageman, G.S.6
Cibis, G.W.7
Ritter III, R.8
Edwards, A.O.9
-
60
-
-
0035168415
-
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
-
(2001)
Nat. Genet.
, vol.27
, pp. 89-93
-
-
Zhang, K.1
Kniazeva, M.2
Han, M.3
Li, W.4
Yu, Z.5
Yang, Z.6
Li, Y.7
Metzker, M.L.8
Allikmets, R.9
Zack, D.J.10
-
61
-
-
0032468842
-
Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q
-
(1998)
Arch. Ophthalmol.
, vol.116
, pp. 1082-1088
-
-
Klein, M.L.1
Schultz, D.W.2
Edwards, A.3
Matise, T.C.4
Rust, K.5
Berselli, C.B.6
Trzupek, K.7
Weleber, R.G.8
Ott, J.9
Wirtz, M.K.10
Acott, T.S.11
-
63
-
-
0034702032
-
A full genome scan for age-related maculopathy
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1329-1349
-
-
Weeks, D.E.1
Conley, Y.P.2
Mah, T.S.3
Paul, T.O.4
Morse, L.5
Ngo-Chang, J.6
Dailey, J.P.7
Ferrell, R.E.8
Gorin, M.B.9
-
74
-
-
0021846717
-
Pathogenetic factors of aging macular degeneration
-
(1985)
Ophthalmology
, vol.92
, pp. 628-635
-
-
Tso, M.O.1
-
83
-
-
0027397668
-
Antioxidant status and neovascular age-related macular degeneration
-
Eye Disease Case Control Study Group
-
(1993)
Arch. Ophthalmol.
, vol.111
, pp. 104-109
-
-
|