-
1
-
-
0001790180
-
A fundus dystrophy with unusual features
-
Sorsby A, Mason ME. A fundus dystrophy with unusual features. Br J Ophthalmol. 1949;33:67–97.
-
(1949)
Br J Ophthalmol
, vol.33
, pp. 67-97
-
-
Sorsby, A.1
Mason, M.E.2
-
2
-
-
0028097367
-
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby’s fundus dystrophy
-
Weber BH, Vogt G, Pruett RC, Stohr H, Felbor U. Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby’s fundus dystrophy. Nat Genet. 1994;8:352–356.
-
(1994)
Nat Genet
, vol.8
, pp. 352-356
-
-
Weber, B.H.1
Vogt, G.2
Pruett, R.C.3
Stohr, H.4
Felbor, U.5
-
3
-
-
24244439671
-
Localization of TIMP-3 mRNA expression to the retinal pigment epithelium
-
Della NG, Campochiaro PA, Zack DJ. Localization of TIMP-3 mRNA expression to the retinal pigment epithelium. Invest Ophthalmol Vis Sci. 1996;37:1921–1924.
-
(1996)
Invest Ophthalmol Vis Sci
, vol.37
, pp. 1921-1924
-
-
Della, N.G.1
Campochiaro, P.A.2
Zack, D.J.3
-
4
-
-
0031013169
-
Tissue inhibitor of metalloproteinases-3 is a component of Bruch’s membrane of the eye
-
Fariss RN, Apte SS, Olsen BR, Iwata K, Milam AH. Tissue inhibitor of metalloproteinases-3 is a component of Bruch’s membrane of the eye. Am J Pathol. 1997;150:323–328.
-
(1997)
Am J Pathol
, vol.150
, pp. 323-328
-
-
Fariss, R.N.1
Apte, S.S.2
Olsen, B.R.3
Iwata, K.4
Milam, A.H.5
-
5
-
-
77049113770
-
The tissue inhibitors of metalloproteinases (TIMPs): An ancient family with structural and functional diversity
-
Brew K, Nagase H. The tissue inhibitors of metalloproteinases (TIMPs): an ancient family with structural and functional diversity. Biochim Biophys Acta. 2010;1803:55–71.
-
(2010)
Biochim Biophys Acta
, vol.1803
, pp. 55-71
-
-
Brew, K.1
Nagase, H.2
-
6
-
-
0037393850
-
A novel function for tissue inhibitor of metalloproteinases-3 (TIMP3): Inhibition of angiogenesis by blockage of VEGF binding to VEGF receptor-2
-
Qi JH, Ebrahem Q, Moore N, et al. A novel function for tissue inhibitor of metalloproteinases-3 (TIMP3): inhibition of angiogenesis by blockage of VEGF binding to VEGF receptor-2. Nat Med. 2003;9:407–415.
-
(2003)
Nat Med
, vol.9
, pp. 407-415
-
-
Qi, J.H.1
Ebrahem, Q.2
Moore, N.3
-
7
-
-
4444380994
-
TIMP3 checks inflammation
-
Black RA. TIMP3 checks inflammation. Nat Genet. 2004;36: 934–935.
-
(2004)
Nat Genet
, vol.36
, pp. 934-935
-
-
Black, R.A.1
-
8
-
-
84855948699
-
A review and update on the molecular basis of pathogenesis of Sorsby fundus dystrophy
-
Stohr H, Anand-Apte B. A review and update on the molecular basis of pathogenesis of Sorsby fundus dystrophy. Adv Exp Med Biol. 2012;723:261–267.
-
(2012)
Adv Exp Med Biol
, vol.723
, pp. 261-267
-
-
Stohr, H.1
Anand-Apte, B.2
-
9
-
-
0026594455
-
Abnormal dark adaptation and rhodopsin kinetics in Sorsby’s fundus dystrophy
-
Steinmetz RL, Polkinghorne PC, Fitzke FW, Kemp CM, Bird AC. Abnormal dark adaptation and rhodopsin kinetics in Sorsby’s fundus dystrophy. Invest Ophthalmol Vis Sci. 1992;33:1633–1636.
-
(1992)
Invest Ophthalmol Vis Sci
, vol.33
, pp. 1633-1636
-
-
Steinmetz, R.L.1
Polkinghorne, P.C.2
Fitzke, F.W.3
Kemp, C.M.4
Bird, A.C.5
-
10
-
-
47549086860
-
Clinical course and treatment outcomes of Sorsby fundus dystrophy
-
Sivaprasad S, Webster AR, Egan CA, Bird AC, Tufail A. Clinical course and treatment outcomes of Sorsby fundus dystrophy. Am J Ophthalmol. 2008;146:228–234.
-
(2008)
Am J Ophthalmol
, vol.146
, pp. 228-234
-
-
Sivaprasad, S.1
Webster, A.R.2
Egan, C.A.3
Bird, A.C.4
Tufail, A.5
-
11
-
-
0024821434
-
Sorsby’s fundus dystrophy. A light and electron microscopic study
-
Capon MR, Marshall J, Krafft JI, Alexander RA, Hiscott PS, Bird AC. Sorsby’s fundus dystrophy. A light and electron microscopic study. Ophthalmology. 1989;96:1769–1777.
-
(1989)
Ophthalmology
, vol.96
, pp. 1769-1777
-
-
Capon, M.R.1
Marshall, J.2
Krafft, J.I.3
Alexander, R.A.4
Hiscott, P.S.5
Bird, A.C.6
-
12
-
-
0019779621
-
Sorsby’s pseudoinflammatory macular dystrophy
-
Hoskin A, Sehmi K, Bird AC. Sorsby’s pseudoinflammatory macular dystrophy. Br J Ophthalmol. 1981;65:859–865.
-
(1981)
Br J Ophthalmol
, vol.65
, pp. 859-865
-
-
Hoskin, A.1
Sehmi, K.2
Bird, A.C.3
-
13
-
-
0030028627
-
A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby’s fundus dystrophy
-
Felbor U, Stohr H, Amann T, Schonherr U, Apfelstedt-Sylla E, Weber BH. A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby’s fundus dystrophy. J Med Genet. 1996;33:233–236.
-
(1996)
J Med Genet
, vol.33
, pp. 233-236
-
-
Felbor, U.1
Stohr, H.2
Amann, T.3
Schonherr, U.4
Apfelstedt-Sylla, E.5
Weber, B.H.6
-
14
-
-
84893164403
-
Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: The example of retinal dystrophies
-
Eisenberger T, Neuhaus C, Khan AO, et al. Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies. PLoS One. 2013;8:78496.
-
(2013)
Plos One
, vol.8
, pp. 78496
-
-
Eisenberger, T.1
Neuhaus, C.2
Khan, A.O.3
-
15
-
-
77955151784
-
MutationTaster evaluates disease-causing potential of sequence alterations
-
Schwarz JM, Rodelsperger C, Schuelke M, Seelow D. MutationTaster evaluates disease-causing potential of sequence alterations. Nat Methods. 2010;7:575–576.
-
(2010)
Nat Methods
, vol.7
, pp. 575-576
-
-
Schwarz, J.M.1
Rodelsperger, C.2
Schuelke, M.3
Seelow, D.4
-
16
-
-
0043122919
-
SIFT: Predicting amino acid changes that affect protein function
-
Ng PC, Henikoff S. SIFT: Predicting amino acid changes that affect protein function. Nucleic Acids Res. 2003;31:3812–3814.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3812-3814
-
-
Ng, P.C.1
Henikoff, S.2
-
17
-
-
84878799611
-
Predicting functional effect of human missense mutations using PolyPhen-2
-
Adzhubei I, Jordan DM, Sunyaev SR. Predicting functional effect of human missense mutations using PolyPhen-2. Curr Protoc Hum Genet. 2013;76:7.1–7.
-
(2013)
Curr Protoc Hum Genet
, vol.76
, Issue.7
, pp. 1-7
-
-
Adzhubei, I.1
Jordan, D.M.2
Sunyaev, S.R.3
-
18
-
-
84855999557
-
Semiautomated image processing method for identification and quantification of geographic atrophy in age-related macular degeneration
-
Schmitz-Valckenberg S, Brinkmann CK, Alten F, et al. Semiautomated image processing method for identification and quantification of geographic atrophy in age-related macular degeneration. Invest Ophthalmol Vis Sci. 2011;52:7640–7646.
-
(2011)
Invest Ophthalmol Vis Sci
, vol.52
, pp. 7640-7646
-
-
Schmitz-Valckenberg, S.1
Brinkmann, C.K.2
Alten, F.3
-
19
-
-
84878029943
-
Atypical Sorsby fundus dystrophy with a novel Tyr159Cys TIMP-3 mutation
-
Fung AT, Stohr H, Weber BF, Holz FG, Yannuzzi LA. Atypical Sorsby fundus dystrophy with a novel Tyr159Cys TIMP-3 mutation. Retin Cases Brief Rep. 2013;7:71–74.
-
(2013)
Retin Cases Brief Rep
, vol.7
, pp. 71-74
-
-
Fung, A.T.1
Stohr, H.2
Weber, B.F.3
Holz, F.G.4
Yannuzzi, L.A.5
-
20
-
-
77954348695
-
Centrifugal fundus abnormalities in pseudoxanthoma elasticum
-
Charbel Issa P, Finger RP, Gotting C, Hendig D, Holz FG, Scholl HP. Centrifugal fundus abnormalities in pseudoxanthoma elasticum. Ophthalmology. 2010;117:1406–1414.
-
(2010)
Ophthalmology
, vol.117
, pp. 1406-1414
-
-
Charbel Issa, P.1
Finger, R.P.2
Gotting, C.3
Hendig, D.4
Holz, F.G.5
Scholl, H.P.6
-
21
-
-
16844386990
-
A novel TIMP3 mutation associated with Sorsby fundus dystrophy
-
Barbazetto IA, Hayashi M, Klais CM, Yannuzzi LA, Allikmets R. A novel TIMP3 mutation associated with Sorsby fundus dystrophy. Arch Ophthalmol. 2005;123:542–543.
-
(2005)
Arch Ophthalmol
, vol.123
, pp. 542-543
-
-
Barbazetto, I.A.1
Hayashi, M.2
Klais, C.M.3
Yannuzzi, L.A.4
Allikmets, R.5
-
22
-
-
0035677969
-
Clinical features of a novel TIMP-3 mutation causing Sorsby’s fundus dystrophy: Implications for disease mechanism
-
Clarke M, Mitchell KW, Goodship J, et al. Clinical features of a novel TIMP-3 mutation causing Sorsby’s fundus dystrophy: implications for disease mechanism. Br J Ophthalmol. 2001; 85:1429–1431.
-
(2001)
Br J Ophthalmol
, vol.85
, pp. 1429-1431
-
-
Clarke, M.1
Mitchell, K.W.2
Goodship, J.3
-
23
-
-
0031468856
-
Sorsby fundus dystrophy: Reevaluation of variable expressivity in patients carrying a TIMP3 founder mutation
-
Felbor U, Benkwitz C, Klein ML, Greenberg J, Gregory CY, Weber BH. Sorsby fundus dystrophy: reevaluation of variable expressivity in patients carrying a TIMP3 founder mutation. Arch Ophthalmol. 1997;115:1569–1571.
-
(1997)
Arch Ophthalmol
, vol.115
, pp. 1569-1571
-
-
Felbor, U.1
Benkwitz, C.2
Klein, M.L.3
Greenberg, J.4
Gregory, C.Y.5
Weber, B.H.6
-
24
-
-
0028879866
-
A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby’s fundus dystrophy with unusual clinical features
-
Felbor U, Stohr H, Amann T, Schonherr U, Weber BH. A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby’s fundus dystrophy with unusual clinical features. Hum Mol Genet. 1995;4:2415–2416.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2415-2416
-
-
Felbor, U.1
Stohr, H.2
Amann, T.3
Schonherr, U.4
Weber, B.H.5
-
25
-
-
0036131152
-
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy
-
Jacobson SG, Cideciyan AV, Bennett J, Kingsley RM, Sheffield VC, Stone EM. Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy. Arch Ophthalmol. 2002;120:376–379.
-
(2002)
Arch Ophthalmol
, vol.120
, pp. 376-379
-
-
Jacobson, S.G.1
Cideciyan, A.V.2
Bennett, J.3
Kingsley, R.M.4
Sheffield, V.C.5
Stone, E.M.6
-
26
-
-
0029114249
-
Night blindness in Sorsby’s fundus dystrophy reversed by vitamin A
-
Jacobson SG, Cideciyan AV, Regunath G, et al. Night blindness in Sorsby’s fundus dystrophy reversed by vitamin A. Nat Genet. 1995;11:27–32.
-
(1995)
Nat Genet
, vol.11
, pp. 27-32
-
-
Jacobson, S.G.1
Cideciyan, A.V.2
Regunath, G.3
-
27
-
-
33750070028
-
A novel His158Arg mutation in TIMP3 causes a late-onset form of Sorsby fundus dystrophy
-
Lin RJ, Blumenkranz MS, Binkley J, Wu K, Vollrath D. A novel His158Arg mutation in TIMP3 causes a late-onset form of Sorsby fundus dystrophy. Am J Ophthalmol. 2006;142:839–848.
-
(2006)
Am J Ophthalmol
, vol.142
, pp. 839-848
-
-
Lin, R.J.1
Blumenkranz, M.S.2
Binkley, J.3
Wu, K.4
Vollrath, D.5
-
28
-
-
67650073274
-
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy
-
Saihan Z, Li Z, Rice J, et al. Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy. Mol Vis. 2009;15:1218–1230.
-
(2009)
Mol Vis
, vol.15
, pp. 1218-1230
-
-
Saihan, Z.1
Li, Z.2
Rice, J.3
-
29
-
-
84873405997
-
A novel mutation at the Nterminal domain of the TIMP3 gene in Sorsby fundus dystrophy
-
Schoenberger SD, Agarwal A. A novel mutation at the Nterminal domain of the TIMP3 gene in Sorsby fundus dystrophy. Retina. 2013;33:429–435.
-
(2013)
Retina
, vol.33
, pp. 429-435
-
-
Schoenberger, S.D.1
Agarwal, A.2
-
30
-
-
0031668129
-
A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby’s fundus dystrophy with unusual clinical features
-
Tabata Y, Isashiki Y, Kamimura K, Nakao K, Ohba N. A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby’s fundus dystrophy with unusual clinical features. Hum Genet. 1998;103:179–182.
-
(1998)
Hum Genet
, vol.103
, pp. 179-182
-
-
Tabata, Y.1
Isashiki, Y.2
Kamimura, K.3
Nakao, K.4
Ohba, N.5
-
31
-
-
77956389326
-
Dominant mut ations in RP1L1 are responsible for occult macular dystrophy
-
Akahori M, Tsunoda K, Miyake Y, et al. Dominant mut ations in RP1L1 are responsible for occult macular dystrophy. Am J Hum Genet. 2010;87:424–429.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 424-429
-
-
Akahori, M.1
Tsunoda, K.2
Miyake, Y.3
-
32
-
-
84873988099
-
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa a nd occult macular dystrophy
-
Davidson AE, Sergouniotis P I, Mackay DS, et al. RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa a nd occult macular dystrophy. Hum Mutat. 2013;34:506–514.
-
(2013)
Hum Mutat
, vol.34
, pp. 506-514
-
-
Davidson, A.E.1
Sergouniotis, P.I.2
Mackay, D.S.3
-
33
-
-
84856092778
-
Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases
-
Audo I, Bujakowska KM, Leveillard T, et al. Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet J Rare Dis. 2012;7:8.
-
(2012)
Orphanet J Rare Dis
, vol.7
, pp. 8
-
-
Audo, I.1
Bujakowska, K.M.2
Leveillard, T.3
-
34
-
-
84876269118
-
An update on the ocular phenotype in patient s with pseudoxanthoma elasticum
-
Gliem M, Zaeytijd JD, Finger RP, Holz FG, Leroy BP, Charbel Issa P. An update on the ocular phenotype in patient s with pseudoxanthoma elasticum. Front Genet. 2013;4:14.
-
(2013)
Front Genet
, vol.4
, pp. 14
-
-
Gliem, M.1
Zaeytijd, J.D.2
Finger, R.P.3
Holz, F.G.4
Leroy, B.P.5
Charbel Issa, P.6
-
35
-
-
0031834379
-
Histologic localization of indocyanine green dye in aging primate and human ocular tissues with clinical angiographic correlation
-
Chang AA, Morse LS, Handa JT, et al. Histologic localization of indocyanine green dye in aging primate and human ocular tissues with clinical angiographic correlation. Ophthalmology. 1998;105:1060–1068.
-
(1998)
Ophthalmology
, vol.105
, pp. 1060-1068
-
-
Chang, A.A.1
Morse, L.S.2
Handa, J.T.3
-
36
-
-
18244391492
-
The interaction of indocyanine green with human retinal pigment epithelium
-
Chang AA, Zhu M, Billson F. The interaction of indocyanine green with human retinal pigment epithelium. Invest Ophthalmol Vis Sci. 2005;46:1463–1467.
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 1463-1467
-
-
Chang, A.A.1
Zhu, M.2
Billson, F.3
-
38
-
-
0023857467
-
Sorsby’s pseudoinflammatory macula dystrophy—Sorsby’s fundus dystrophies
-
Capon MR, Polkinghorne PJ, Fitzke FW, Bird AC. Sorsby’s pseudoinflammatory macula dystrophy—Sorsby’s fundus dystrophies. Eye (Lond). 1988;2;114–122.
-
(1988)
Eye (Lond)
, vol.2
, pp. 114-122
-
-
Capon, M.R.1
Polkinghorne, P.J.2
Fitzke, F.W.3
Bird, A.C.4
-
39
-
-
0024830978
-
Sorsby’s fundus dystrophy. A clinical study
-
Polkinghorne PJ, Capon MR, Berninger T, Lyness AL, Sehmi K, Bird AC. Sorsby’s fundus dystrophy. A clinical study. Ophthalmology. 1989;96:1763–1768.
-
(1989)
Ophthalmology
, vol.96
, pp. 1763-1768
-
-
Polkinghorne, P.J.1
Capon, M.R.2
Berninger, T.3
Lyness, A.L.4
Sehmi, K.5
Bird, A.C.6
-
40
-
-
0029563246
-
Sorsby’s fundus dystrophy. A South African family with a point mutation on the tissue inhibitor of metalloproteinases-3 gene on chromosome 22
-
Peters AL, Greenberg J. Sorsby’s fundus dystrophy. A South African family with a point mutation on the tissue inhibitor of metalloproteinases-3 gene on chromosome 22. Retina. 1995; 15:480–485.
-
(1995)
Retina
, vol.15
, pp. 480-485
-
-
Peters, A.L.1
Greenberg, J.2
-
41
-
-
0029947143
-
Sorsby fundus dystrophy. A family with the Ser181Cys mutation of the tissue inhibitor of metalloproteinases 3
-
Carrero-Valenzuela RD, Klein ML, Weleber RG, Murphey WH, Litt M. Sorsby fundus dystrophy. A family with the Ser181Cys mutation of the tissue inhibitor of metalloproteinases 3. Arch Ophthalmol. 1996;114:737–738.
-
(1996)
Arch Ophthalmol
, vol.114
, pp. 737-738
-
-
Carrero-Valenzuela, R.D.1
Klein, M.L.2
Weleber, R.G.3
Murphey, W.H.4
Litt, M.5
-
43
-
-
0031038238
-
Autosomal recessive Sorsby fundus dystrophy revisited: Molecular evidence for dominant inheritance
-
Felbor U, Suvanto EA, Forsius HR, Eriksson AW, Weber BH. Autosomal recessive Sorsby fundus dystrophy revisited: molecular evidence for dominant inheritance. Am J Hum Genet. 1997;60:57–62.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 57-62
-
-
Felbor, U.1
Suvanto, E.A.2
Forsius, H.R.3
Eriksson, A.W.4
Weber, B.H.5
-
46
-
-
0034282898
-
A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby’s fundus dystrophy
-
Langton KP, McKie N, Curtis A, et al. A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby’s fundus dystrophy. J Biol Chem. 2000; 275:27027–27031.
-
(2000)
J Biol Chem
, vol.275
, pp. 27027-27031
-
-
Langton, K.P.1
McKie, N.2
Curtis, A.3
-
47
-
-
0032754555
-
Sorsby’s fundus dystrophy in two Japanese families with unusual clinical features
-
Isashiki Y, Tabata Y, Kamimura K, Ohba N. Sorsby’s fundus dystrophy in two Japanese families with unusual clinical features. Jpn J Ophthalmol. 1999;43:472–480.
-
(1999)
Jpn J Ophthalmol
, vol.43
, pp. 472-480
-
-
Isashiki, Y.1
Tabata, Y.2
Kamimura, K.3
Ohba, N.4
-
49
-
-
0015081142
-
Sorsby’s familial pseudo-inflammatory macular dystrophy
-
Fraser HB, Wallace DC. Sorsby’s familial pseudo-inflammatory macular dystrophy. Am J Ophthalmol. 1971;71:1216–1220.
-
(1971)
Am J Ophthalmol
, vol.71
, pp. 1216-1220
-
-
Fraser, H.B.1
Wallace, D.C.2
-
50
-
-
33847073347
-
Progression of geographic atrophy and impact of fundus autofluorescence patterns in age-related macular degeneration
-
Holz FG, Bindewald-Wittich A, Fleckenstein M, Dreyhaupt J, Scholl HP, Schmitz-Valckenberg S. Progression of geographic atrophy and impact of fundus autofluorescence patterns in age-related macular degeneration. Am J Ophthalmol. 2007; 143:463–472.
-
(2007)
Am J Ophthalmol
, vol.143
, pp. 463-472
-
-
Holz, F.G.1
Bindewald-Wittich, A.2
Fleckenstein, M.3
Dreyhaupt, J.4
Scholl, H.P.5
Schmitz-Valckenberg, S.6
-
51
-
-
77955469874
-
Progression of geographic atrophy and genotype in age-related macular degeneration
-
Klein ML, Ferris FL III, Francis PJ, et al. Progression of geographic atrophy and genotype in age-related macular degeneration. Ophthalmology. 2010;117:1554–1559.
-
(2010)
Ophthalmology
, vol.117
, pp. 1554-1559
-
-
Klein, M.L.1
Ferris, F.2
Francis, P.J.3
-
52
-
-
84877745361
-
A longitudinal study of Stargardt disease: Clinical and electrophysiologic assessme nt,progression, and genotype correlations
-
Fujinami K, Lois N, Davidson AE, et al. A longitudinal study of Stargardt disease: clinical and electrophysiologic assessme nt,progression, and genotype correlations. Am J Ophthalmol. 2013;155:1075–1088.
-
(2013)
Am J Ophthalmol
, vol.155
, pp. 1075-1088
-
-
Fujinami, K.1
Lois, N.2
Davidson, A.E.3
-
53
-
-
77954955124
-
Analysis of autofluorescent retinal images and measurement of atrophic lesion growth in Stargardt disease
-
Chen B, Tosha C, Gorin MB, Nusinowitz S. Analysis of autofluorescent retinal images and measurement of atrophic lesion growth in Stargardt disease. Exp Eye Res. 2010;91:143–152.
-
(2010)
Exp Eye Res
, vol.91
, pp. 143-152
-
-
Chen, B.1
Tosha, C.2
Gorin, M.B.3
Nusinowitz, S.4
-
54
-
-
84862761654
-
Progression of retinal pigment epithelial atrophy in Stargardt disease
-
McBain VA, Townend J, Lois N. Progression of retinal pigment epithelial atrophy in Stargardt disease. Am J Ophthalmol. 2012;154:146–154.
-
(2012)
Am J Ophthalmol
, vol.154
, pp. 146-154
-
-
McBain, V.A.1
Townend, J.2
Lois, N.3
-
55
-
-
84902532201
-
Choroidal changes associated with Bruch membrane pathology in pseudoxanthoma elasticum
-
Gliem M, Fimmers R, Muller PL, et al. Choroidal changes associated with Bruch membrane pathology in pseudoxanthoma elasticum. Am J Ophthalmol. 2014;158:198–207.
-
(2014)
Am J Ophthalmol
, vol.158
, pp. 198-207
-
-
Gliem, M.1
Fimmers, R.2
Muller, P.L.3
-
56
-
-
84872246066
-
Ranibizumab for the management of Sorsby fundus dystrophy
-
Balaskas K, Hovan M, Mahmood S, Bishop P. Ranibizumab for the management of Sorsby fundus dystrophy. Eye (Lond). 2013;27:101–102.
-
(2013)
Eye (Lond)
, vol.27
, pp. 101-102
-
-
Balaskas, K.1
Hovan, M.2
Mahmood, S.3
Bishop, P.4
-
57
-
-
84880553000
-
Intravitreal anti-vascular endothelial growth factor therapy for choroidal neovascularization due to Sorsby macular dystrophy
-
Kapoor KG, Bakri SJ. Intravitreal anti-vascular endothelial growth factor therapy for choroidal neovascularization due to Sorsby macular dystrophy. J Ocul Pharmacol Ther. 2013;29: 444–447.
-
(2013)
J Ocul Pharmacol Ther
, vol.29
, pp. 444-447
-
-
Kapoor, K.G.1
Bakri, S.J.2
-
58
-
-
84862548278
-
Choroidal neovascularization secondary to Sorsby fundus dsytrophy treated with intravitreal bevacizumab
-
Gray TL, Wong H, Raymond GL. Choroidal neovascularization secondary to Sorsby fundus dsytrophy treated with intravitreal bevacizumab. Retin Cases Brief Rep. 2012;6:193–196.
-
(2012)
Retin Cases Brief Rep
, vol.6
, pp. 193-196
-
-
Gray, T.L.1
Wong, H.2
Raymond, G.L.3
-
59
-
-
84856409039
-
Successful treatment of choroidal neovascularization secondary to Sorsby fundus dystrophy with intravitreal bevacizumab
-
Gemenetzi MK, Luff AJ, Lotery AJ. Successful treatment of choroidal neovascularization secondary to Sorsby fundus dystrophy with intravitreal bevacizumab. Retin Cases Brief Rep. 2011;5:132–135.
-
(2011)
Retin Cases Brief Rep
, vol.5
, pp. 132-135
-
-
Gemenetzi, M.K.1
Luff, A.J.2
Lotery, A.J.3
-
60
-
-
0028050354
-
Recurrent choroidal neovascularization after laser photocoagulation in Sorsby’s fundus dystrophy
-
Holz FG, Haimovici R, Wagner DG, Bird AC. Recurrent choroidal neovascularization after laser photocoagulation in Sorsby’s fundus dystrophy. Retina. 1994;14:329–334.
-
(1994)
Retina
, vol.14
, pp. 329-334
-
-
Holz, F.G.1
Haimovici, R.2
Wagner, D.G.3
Bird, A.C.4
-
61
-
-
0032909397
-
Safety of <7500 RE (<25000 IU) vitamin A daily in adults with retinitis pigmentosa
-
Sibulesky L, Hayes KC, Pronczuk A, Weigel-DiFranco C, Rosner B, Berson EL. Safety of <7500 RE (<25000 IU) vitamin A daily in adults with retinitis pigmentosa. Am J Clin Nutr. 1999;69: 656–663.
-
(1999)
Am J Clin Nutr
, vol.69
, pp. 656-663
-
-
Sibulesky, L.1
Hayes, K.C.2
Pronczuk, A.3
Weigel-Difranco, C.4
Rosner, B.5
Berson, E.L.6
|