-
1
-
-
0347581233
-
The molecular genetics of the corneal dystrophies - current status
-
Klintworth GK. The molecular genetics of the corneal dystrophies - current status. Front Biosci. 2003;8:d687-713.
-
(2003)
Front Biosci
, vol.8
-
-
Klintworth, G.K.1
-
2
-
-
0027963514
-
Familial cases of keratoconus associated with posterior polymorphous dystrophy
-
Driver PJ, Reed JW, Davis RM. Familial cases of keratoconus associated with posterior polymorphous dystrophy. Am J Ophthalmol. 1994;118:256-257.
-
(1994)
Am J Ophthalmol
, vol.118
, pp. 256-257
-
-
Driver, P.J.1
Reed, J.W.2
Davis, R.M.3
-
3
-
-
0026532983
-
Bilateral progressive essential iris atrophy and keratoconus with coincident features of posterior polymorphous dystrophy: A case report and proposed pathogenesis
-
Blair SD, Seabrooks D, Shields WJ, et al. Bilateral progressive essential iris atrophy and keratoconus with coincident features of posterior polymorphous dystrophy: a case report and proposed pathogenesis. Cornea. 1992;11:255-261.
-
(1992)
Cornea
, vol.11
, pp. 255-261
-
-
Blair, S.D.1
Seabrooks, D.2
Shields, W.J.3
-
5
-
-
0024517291
-
Four cases of keratoconus and posterior polymorphous corneal dystrophy
-
Weissman BA, Ehrlich M, Levenson JE, et al. Four cases of keratoconus and posterior polymorphous corneal dystrophy. Optom Vis Sci. 1989;66:243-246.
-
(1989)
Optom Vis Sci
, vol.66
, pp. 243-246
-
-
Weissman, B.A.1
Ehrlich, M.2
Levenson, J.E.3
-
6
-
-
0016260267
-
Posterior polymorphous dystrophy associated with keratoconus
-
Gasset AR, Zimmerman TJ. Posterior polymorphous dystrophy associated with keratoconus. Am J Ophthalmol. 1974;78:535-537.
-
(1974)
Am J Ophthalmol
, vol.78
, pp. 535-537
-
-
Gasset, A.R.1
Zimmerman, T.J.2
-
7
-
-
0032859649
-
Terrien's marginal degeneration associated with posterior polymorphous dystrophy
-
Wagoner MD, Teichmann KD. Terrien's marginal degeneration associated with posterior polymorphous dystrophy. Cornea. 1999;18:612-615.
-
(1999)
Cornea
, vol.18
, pp. 612-615
-
-
Wagoner, M.D.1
Teichmann, K.D.2
-
8
-
-
0021343891
-
Keratoconus and related non-inflammatory corneal thinning disorders
-
Krachmer JH, Feder RS, Belin MW. Keratoconus and related non-inflammatory corneal thinning disorders. Surv Ophthalmol. 1984;28:293-322.
-
(1984)
Surv Ophthalmol
, vol.28
, pp. 293-322
-
-
Krachmer, J.H.1
Feder, R.S.2
Belin, M.W.3
-
11
-
-
33846536782
-
Outcomes of epikeratoplasty for advanced keratoglobus
-
Javadi MA, Kanavi MR, Ahmadi M, et al. Outcomes of epikeratoplasty for advanced keratoglobus. Cornea. 2007;26:154-157.
-
(2007)
Cornea
, vol.26
, pp. 154-157
-
-
Javadi, M.A.1
Kanavi, M.R.2
Ahmadi, M.3
-
13
-
-
33751517374
-
Potential complications of ocular surgery in patients with coexistent keratoconus and Fuchs' endothelial dystrophy
-
Jurkunas U, Azar DT. Potential complications of ocular surgery in patients with coexistent keratoconus and Fuchs' endothelial dystrophy. Ophthalmology. 2006;113:2187-2197.
-
(2006)
Ophthalmology
, vol.113
, pp. 2187-2197
-
-
Jurkunas, U.1
Azar, D.T.2
-
14
-
-
0029835354
-
Topographic analysis in pellucid marginal corneal degeneration and keratoglobus
-
Karabatsas CH, Cook SD. Topographic analysis in pellucid marginal corneal degeneration and keratoglobus. Eye. 1996;10:451-455.
-
(1996)
Eye
, vol.10
, pp. 451-455
-
-
Karabatsas, C.H.1
Cook, S.D.2
-
15
-
-
27244444742
-
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells
-
Krafchak CM, Pawar H, Moroi SE, et al. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells. Am J Hum Genet. 2005;77:694-708.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 694-708
-
-
Krafchak, C.M.1
Pawar, H.2
Moroi, S.E.3
-
16
-
-
0036566556
-
VSX1: A gene for posterior polymorphous dystrophy and keratoconus
-
Heon E, Greenberg A, Kopp KK, et al. VSX1: a gene for posterior polymorphous dystrophy and keratoconus. Hum Mol Genet. 2002;11:1029-1036.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1029-1036
-
-
Heon, E.1
Greenberg, A.2
Kopp, K.K.3
-
17
-
-
19944416896
-
VSX1 mutational analysis in a series of Italian patients affected by keratoconus: Detection of a novel mutation
-
Bisceglia L, Ciaschetti M, De Bonis P, et al. VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. Invest Ophthalmol Vis Sci. 2005;46:39-45.
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 39-45
-
-
Bisceglia, L.1
Ciaschetti, M.2
De Bonis, P.3
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