-
2
-
-
0036014902
-
Mechanisms of disease: Fuchs' endothelial dystrophy
-
Borboli S, Colby K. Mechanisms of disease: Fuchs' endothelial dystrophy. Ophthalmol Clin North Am. 2002;15:17-25.
-
(2002)
Ophthalmol Clin North Am
, vol.15
, pp. 17-25
-
-
Borboli, S.1
Colby, K.2
-
3
-
-
0023712886
-
Endothelial function and aqueous humor flow rate in patients with Fuchs' dystrophy
-
Wilson SE, Bourne WM, O'Brien PC, Brubaker RF. Endothelial function and aqueous humor flow rate in patients with Fuchs' dystrophy. Am J Ophthalmol. 1988;106:270-278.
-
(1988)
Am J Ophthalmol
, vol.106
, pp. 270-278
-
-
Wilson, S.E.1
Bourne, W.M.2
O'Brien, P.C.3
Brubaker, R.F.4
-
5
-
-
0031707463
-
In vivo confocal microscopy of Fuchs' endothelial dystrophy
-
Mustonen RK, McDonald MB, Srivannaboon S, Tan AL, Doubrava MW, Kim CK. In vivo confocal microscopy of Fuchs' endothelial dystrophy. Cornea. 1998;17:493-503.
-
(1998)
Cornea
, vol.17
, pp. 493-503
-
-
Mustonen, R.K.1
McDonald, M.B.2
Srivannaboon, S.3
Tan, A.L.4
Doubrava, M.W.5
Kim, C.K.6
-
7
-
-
0018606624
-
Inheritance of Fuchs' combined dystrophy
-
Magovern M, Beauchamp GR, McTigue JW, Fine BS, Baumiller RC. Inheritance of Fuchs' combined dystrophy. Ophthalmology. 1979;86:1897-1920.
-
(1979)
Ophthalmology
, vol.86
, pp. 1897-1920
-
-
Magovern, M.1
Beauchamp, G.R.2
McTigue, J.W.3
Fine, B.S.4
Baumiller, R.C.5
-
8
-
-
0018909612
-
Hereditary Fuchs' dystrophy
-
Rosenblum P, Stark WJ, Maumenee IH, Hirst LW, Maumenee E. Hereditary Fuchs' dystrophy. Am J Ophthalmol. 1980;90:455-462.
-
(1980)
Am J Ophthalmol
, vol.90
, pp. 455-462
-
-
Rosenblum, P.1
Stark, W.J.2
Maumenee, I.H.3
Hirst, L.W.4
Maumenee, E.5
-
9
-
-
0033987147
-
Three decades of corneal transplantation: Indications and patient characteristics
-
Maeno A, Naor J, Lee HM, Hunter WS, Rootman DS. Three decades of corneal transplantation: indications and patient characteristics. Cornea. 2000;19:7-11.
-
(2000)
Cornea
, vol.19
, pp. 7-11
-
-
Maeno, A.1
Naor, J.2
Lee, H.M.3
Hunter, W.S.4
Rootman, D.S.5
-
10
-
-
0033759339
-
Trends in the indications for penetrating keratoplasty in the midwestern United States
-
Dobbins KRB, Price FW Jr, Whitson WE. Trends in the indications for penetrating keratoplasty in the midwestern United States. Cornea. 2000;19:813-816.
-
(2000)
Cornea
, vol.19
, pp. 813-816
-
-
Dobbins, K.R.B.1
Price Jr., F.W.2
Whitson, W.E.3
-
11
-
-
0030817349
-
Indications for penetrating keratoplasty and associated procedures, 1989-1995
-
Lois N, Kowal VO, Cohen EJ, et al. Indications for penetrating keratoplasty and associated procedures, 1989-1995. Cornea. 1997;16:623-629.
-
(1997)
Cornea
, vol.16
, pp. 623-629
-
-
Lois, N.1
Kowal, V.O.2
Cohen, E.J.3
-
12
-
-
0344269306
-
Changing indications for penetrating keratoplasty: Histopathology of 1,250 corneal buttons
-
Cursiefen C, Küchle M, Naumann GOH. Changing indications for penetrating keratoplasty: histopathology of 1,250 corneal buttons. Cornea. 1998;17:468-470.
-
(1998)
Cornea
, vol.17
, pp. 468-470
-
-
Cursiefen, C.1
Küchle, M.2
Naumann, G.O.H.3
-
13
-
-
0024382286
-
Clinical indications for and procedures associated with penetrating keratoplasty, 1983-1988
-
Brady SE, Rapuano CJ, Arentsen JJ, Cohen EJ, Laibson PR. Clinical indications for and procedures associated with penetrating keratoplasty, 1983-1988. Am J Ophthalmol. 1989;108:118-122.
-
(1989)
Am J Ophthalmol
, vol.108
, pp. 118-122
-
-
Brady, S.E.1
Rapuano, C.J.2
Arentsen, J.J.3
Cohen, E.J.4
Laibson, P.R.5
-
14
-
-
0030817349
-
Indications for penetrating keratoplasty and associated procedures, 1989-1993
-
Lois N, Kowal VO, Cohen EJ, et al. Indications for penetrating keratoplasty and associated procedures, 1989-1993. Cornea. 1997;16:623-629.
-
(1997)
Cornea
, vol.16
, pp. 623-629
-
-
Lois, N.1
Kowal, V.O.2
Cohen, E.J.3
-
16
-
-
25844498420
-
Trends in the indications for penetrating keratoplasty, 1980-2001
-
Kang PC, Klintworth GK, Kim T, et al. Trends in the indications for penetrating keratoplasty, 1980-2001. Cornea. 2005;24:801-803.
-
(2005)
Cornea
, vol.24
, pp. 801-803
-
-
Kang, P.C.1
Klintworth, G.K.2
Kim, T.3
-
18
-
-
0035504694
-
Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
-
Biswas S, Munier FL, Yardley J, et al. Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Hum Mol Genet. 2001;10:2415-2423.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2415-2423
-
-
Biswas, S.1
Munier, F.L.2
Yardley, J.3
|