-
3
-
-
17344362827
-
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
-
Bejjani BA, Lewis RA, Tomey KF, et al. Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia. Am J Hum Genet. 1998;62:325-233.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 325-233
-
-
Bejjani, B.A.1
Lewis, R.A.2
Tomey, K.F.3
-
4
-
-
0034639693
-
-
Bejjani BA, Stockton DW, Lewis RA, et al. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet. 2000;9:367-374. Erratum in: Hum Mol Genet. 2000;9:1141.
-
Bejjani BA, Stockton DW, Lewis RA, et al. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet. 2000;9:367-374. Erratum in: Hum Mol Genet. 2000;9:1141.
-
-
-
-
5
-
-
33846428903
-
Congenital hereditary corneal dystrophy
-
Maumenee AE. Congenital hereditary corneal dystrophy. Am J Ophthalmol. 1960;50:1114-1124.
-
(1960)
Am J Ophthalmol
, vol.50
, pp. 1114-1124
-
-
Maumenee, A.E.1
-
6
-
-
0013815166
-
Congenital hereditary corneal dystrophy
-
Keates RH, Cvintal T. Congenital hereditary corneal dystrophy. Am J Ophthalmol. 1965;60:892-894.
-
(1965)
Am J Ophthalmol
, vol.60
, pp. 892-894
-
-
Keates, R.H.1
Cvintal, T.2
-
7
-
-
0017807244
-
Clinical differentiation of recessive congenital hereditary endothelial dystrophy and dominant hereditary endothelial dystrophy
-
Judisch GF, Maumenee IH. Clinical differentiation of recessive congenital hereditary endothelial dystrophy and dominant hereditary endothelial dystrophy. Am J Ophthalmol. 1978;85(5 Pt 1):606-612.
-
(1978)
Am J Ophthalmol
, vol.85
, Issue.5 PART 1
, pp. 606-612
-
-
Judisch, G.F.1
Maumenee, I.H.2
-
8
-
-
33846310951
-
-
Jiao X, Sultana A, Garg P, et al. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. J Med Genet. 2007;44:64-68. Erratum in: J Med Genet. 2007;44:407.
-
Jiao X, Sultana A, Garg P, et al. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. J Med Genet. 2007;44:64-68. Erratum in: J Med Genet. 2007;44:407.
-
-
-
-
9
-
-
33745544253
-
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
-
Vithana EN, Morgan P, Sundaresan P, et al. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nat Genet. 2006;38:755-757.
-
(2006)
Nat Genet
, vol.38
, pp. 755-757
-
-
Vithana, E.N.1
Morgan, P.2
Sundaresan, P.3
-
10
-
-
0028893448
-
Results of penetrating keratoplasty in CHED: Congenital hereditary endothelial dystrophy
-
Sajjadi H, Javadi MA, Hemmati R, Mirdeghan A, Parvin M, Nassiri N. Results of penetrating keratoplasty in CHED: congenital hereditary endothelial dystrophy. Cornea. 1995;14:18-25.
-
(1995)
Cornea
, vol.14
, pp. 18-25
-
-
Sajjadi, H.1
Javadi, M.A.2
Hemmati, R.3
Mirdeghan, A.4
Parvin, M.5
Nassiri, N.6
-
11
-
-
0027291601
-
Sources of error with use of Goldmann-type tonometers
-
Whitacre MM, Stein R. Sources of error with use of Goldmann-type tonometers. Surv Ophthalmol. 1993;38:1-30.
-
(1993)
Surv Ophthalmol
, vol.38
, pp. 1-30
-
-
Whitacre, M.M.1
Stein, R.2
-
12
-
-
0018575310
-
Increase in axial length of the macaque monkey eye after corneal opacification
-
Wiesel TN, Raviola E. Increase in axial length of the macaque monkey eye after corneal opacification. Invest Ophthalmol Vis Sci. 1979;18:1232-1236.
-
(1979)
Invest Ophthalmol Vis Sci
, vol.18
, pp. 1232-1236
-
-
Wiesel, T.N.1
Raviola, E.2
-
13
-
-
33646901276
-
Measuring intraocular pressure-adjustments for corneal thickness and new technologies
-
Herndon LW. Measuring intraocular pressure-adjustments for corneal thickness and new technologies. Curr Opin Ophthalmol. 2006;17:115-119.
-
(2006)
Curr Opin Ophthalmol
, vol.17
, pp. 115-119
-
-
Herndon, L.W.1
-
15
-
-
35848966791
-
What biomechanical properties of the cornea are relevant for the clinician?
-
Kotecha A. What biomechanical properties of the cornea are relevant for the clinician? Surv Ophthalmol. 2007;52(suppl 2):S109-S114.
-
(2007)
Surv Ophthalmol
, vol.52
, Issue.SUPPL. 2
-
-
Kotecha, A.1
-
16
-
-
39749171797
-
Central corneal thickness in children: Does it help or hinder our evaluation of eyes at risk for glaucoma?
-
Freedman SF. Central corneal thickness in children: does it help or hinder our evaluation of eyes at risk for glaucoma? J AAPOS. 2008;12:1-2.
-
(2008)
J AAPOS
, vol.12
, pp. 1-2
-
-
Freedman, S.F.1
-
17
-
-
0024426247
-
Anterior mesenchymal dysgenesis of the eye: Congenital hereditary endothelial dystrophy and congenital glaucoma
-
Pedersen OO, Rushood A, Olsen EG. Anterior mesenchymal dysgenesis of the eye: congenital hereditary endothelial dystrophy and congenital glaucoma. Acta Ophthalmol (Copenh). 1989;67:470-476.
-
(1989)
Acta Ophthalmol (Copenh)
, vol.67
, pp. 470-476
-
-
Pedersen, O.O.1
Rushood, A.2
Olsen, E.G.3
-
18
-
-
0028838036
-
Congenital hereditary endothelial dystrophy associated with glaucoma
-
Mullaney PB, Risco JM, Teichmann K, Millar L. Congenital hereditary endothelial dystrophy associated with glaucoma. Ophthalmology. 1995;102:186-192.
-
(1995)
Ophthalmology
, vol.102
, pp. 186-192
-
-
Mullaney, P.B.1
Risco, J.M.2
Teichmann, K.3
Millar, L.4
-
19
-
-
34447517518
-
Coexistent congenital hereditary endothelial dystrophy and congenital glaucoma
-
Ramamurthy B, Sachdeva V, Mandal AK, Vemuganti GK, Garg P, Sangwan VS. Coexistent congenital hereditary endothelial dystrophy and congenital glaucoma. Cornea. 2007;26:647-649.
-
(2007)
Cornea
, vol.26
, pp. 647-649
-
-
Ramamurthy, B.1
Sachdeva, V.2
Mandal, A.K.3
Vemuganti, G.K.4
Garg, P.5
Sangwan, V.S.6
-
20
-
-
33847266341
-
Primary pediatric keratoplasty: Indications, graft survival, and visual outcome
-
Al-Ghamdi A, Al-Rajhi A, Wagoner MD. Primary pediatric keratoplasty: indications, graft survival, and visual outcome. J AAPOS. 2007;11:41-47.
-
(2007)
J AAPOS
, vol.11
, pp. 41-47
-
-
Al-Ghamdi, A.1
Al-Rajhi, A.2
Wagoner, M.D.3
-
21
-
-
3342986341
-
Outcome of combined Ahmed glaucoma valve implant and penetrating keratoplasty in refractory congenital glaucoma with corneal opacity
-
Al-Torbak AA. Outcome of combined Ahmed glaucoma valve implant and penetrating keratoplasty in refractory congenital glaucoma with corneal opacity. Cornea. 2004;23:554-559.
-
(2004)
Cornea
, vol.23
, pp. 554-559
-
-
Al-Torbak, A.A.1
|