-
1
-
-
0842331164
-
Scleral structure, organisation and disease. A review
-
Watson PG, Young RD Scleral structure, organisation and disease. A review. Exp Eye Res 2004, 609-623.
-
(2004)
Exp Eye Res
, pp. 609-623
-
-
Watson, P.G.1
Young, R.D.2
-
3
-
-
0014329492
-
Corneal thickness
-
Mishima S Corneal thickness. Surv Ophthalmol 1968, 13(2):57-96.
-
(1968)
Surv Ophthalmol
, vol.13
, Issue.2
, pp. 57-96
-
-
Mishima, S.1
-
4
-
-
0030866375
-
The physical basis of transparency of the normal cornea
-
Freegard TJ The physical basis of transparency of the normal cornea. Eye (Lond) 1997, 11(Pt 4):465-471.
-
(1997)
Eye (Lond)
, vol.11
, Issue.4 PT
, pp. 465-471
-
-
Freegard, T.J.1
-
5
-
-
0026608043
-
An immunoelectron microscope study of the aged human lens capsule
-
Marshall GE, Konstas AG, Bechrakis NE, Lee WR An immunoelectron microscope study of the aged human lens capsule. Esp Eye Res 1992, 54:393-401.
-
(1992)
Esp Eye Res
, vol.54
, pp. 393-401
-
-
Marshall, G.E.1
Konstas, A.G.2
Bechrakis, N.E.3
Lee, W.R.4
-
6
-
-
33746850984
-
-
American Academy of Ophthalmology
-
Regillo C, Holekamp N, Johnson MW, Kaiser PK, Schubert HD, Spaide R, et al. Retina and vitreous 2012, American Academy of Ophthalmology.
-
(2012)
Retina and vitreous
-
-
Regillo, C.1
Holekamp, N.2
Johnson, M.W.3
Kaiser, P.K.4
Schubert, H.D.5
Spaide, R.6
-
7
-
-
0005532045
-
Osteogenesis imperfecta congenita and blue sclerotics; a clinicopathologic study
-
Ruedemann AD Osteogenesis imperfecta congenita and blue sclerotics; a clinicopathologic study. AMA Arch Ophthalmol 1953, 6-16.
-
(1953)
AMA Arch Ophthalmol
, pp. 6-16
-
-
Ruedemann, A.D.1
-
8
-
-
76549203834
-
Ocular anomalies in osteogenesis imperfecta
-
Manschot WA Ocular anomalies in osteogenesis imperfecta. Ophthalmologica 1965, 241-245.
-
(1965)
Ophthalmologica
, pp. 241-245
-
-
Manschot, W.A.1
-
9
-
-
84980148209
-
An autopsy case of osteogenesis imperfecta congenita - histochemical and electron microscopical studies
-
Haebara H, Yamasaki Y, Kyogoku M An autopsy case of osteogenesis imperfecta congenita - histochemical and electron microscopical studies. Acta Pathol Jpn 1969, 377-394.
-
(1969)
Acta Pathol Jpn
, pp. 377-394
-
-
Haebara, H.1
Yamasaki, Y.2
Kyogoku, M.3
-
10
-
-
0015448928
-
Histochemical and fine structural studies on the cornea with osteogenesis imperfecta congenita
-
Blümcke S, Niedorf HR, Thiel HJ, Langness U Histochemical and fine structural studies on the cornea with osteogenesis imperfecta congenita. Virchows Arch B Cell Pathol 1972, 124-132.
-
(1972)
Virchows Arch B Cell Pathol
, pp. 124-132
-
-
Blümcke, S.1
Niedorf, H.R.2
Thiel, H.J.3
Langness, U.4
-
12
-
-
0027419527
-
Agenesis of Bowman's layer. A histopathological study of four cases
-
Kasner L, Mietz H, Green WR Agenesis of Bowman's layer. A histopathological study of four cases. Cornea 1993, 163-170.
-
(1993)
Cornea
, pp. 163-170
-
-
Kasner, L.1
Mietz, H.2
Green, W.R.3
-
13
-
-
0030842916
-
Histopathologic and electron-microscopic features of corneal and scleral collagen fibers in osteogenesis imperfecta type III
-
Mietz H, Kasner L, Green WR Histopathologic and electron-microscopic features of corneal and scleral collagen fibers in osteogenesis imperfecta type III. Graefes Arch Clin Exp Ophthalmol 1997, 405-410.
-
(1997)
Graefes Arch Clin Exp Ophthalmol
, pp. 405-410
-
-
Mietz, H.1
Kasner, L.2
Green, W.R.3
-
14
-
-
0021358464
-
Central corneal thickness in osteogenesis imperfecta and otosclerosis
-
Pedersen U, Bramsen T Central corneal thickness in osteogenesis imperfecta and otosclerosis. ORL J Otorhinolaryngol Relat Spec 1984, 38-41.
-
(1984)
ORL J Otorhinolaryngol Relat Spec
, pp. 38-41
-
-
Pedersen, U.1
Bramsen, T.2
-
15
-
-
0036831828
-
Central corneal thickness is lower in osteogenesis imperfecta and negatively correlates with the presence of blue sclera
-
Evereklioglu C, Madenci E, Bayazit YA, Yilmaz K, Balat A, Bekir NA Central corneal thickness is lower in osteogenesis imperfecta and negatively correlates with the presence of blue sclera. Ophthalmic Physiol Opt 2002, 511-515.
-
(2002)
Ophthalmic Physiol Opt
, pp. 511-515
-
-
Evereklioglu, C.1
Madenci, E.2
Bayazit, Y.A.3
Yilmaz, K.4
Balat, A.5
Bekir, N.A.6
-
16
-
-
77449119555
-
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
-
Dimasi DP, Chen JY, Hewitt AW, Klebe S, Davey R, Stirling J, et al. Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes. Hum Genet 2010, 33-44.
-
(2010)
Hum Genet
, pp. 33-44
-
-
Dimasi, D.P.1
Chen, J.Y.2
Hewitt, A.W.3
Klebe, S.4
Davey, R.5
Stirling, J.6
-
17
-
-
0029286338
-
Autosomal dominant keratoconus as the chief ocular symptom in Lobstein osteogenesis imperfecta tarda
-
Beckh U, Schönherr U, Naumann GO Autosomal dominant keratoconus as the chief ocular symptom in Lobstein osteogenesis imperfecta tarda. Klin Monatsbl Augenheilkd 1995, 268-272.
-
(1995)
Klin Monatsbl Augenheilkd
, pp. 268-272
-
-
Beckh, U.1
Schönherr, U.2
Naumann, G.O.3
-
18
-
-
0023911794
-
Comparative studies of collagens in normal and keratoconus corneas
-
Zimmermann DR, Fischer RW, Winterhalter KH, Witmer R, Vaughan L Comparative studies of collagens in normal and keratoconus corneas. Exp Eye Res 1988, 431-442.
-
(1988)
Exp Eye Res
, pp. 431-442
-
-
Zimmermann, D.R.1
Fischer, R.W.2
Winterhalter, K.H.3
Witmer, R.4
Vaughan, L.5
-
19
-
-
0014446640
-
Blue sclerae and keratoglobus. Ocular signs of a systemic connective tissue disorder
-
Hyams SW, Kar H, Neumann E Blue sclerae and keratoglobus. Ocular signs of a systemic connective tissue disorder. Brit J Ophthalmol 1969, 53-58.
-
(1969)
Brit J Ophthalmol
, pp. 53-58
-
-
Hyams, S.W.1
Kar, H.2
Neumann, E.3
-
21
-
-
76549219980
-
The syndrome of blue sclerae with keratoglobus
-
Arkin W The syndrome of blue sclerae with keratoglobus. Klin Oczna 1965, 89-93.
-
(1965)
Klin Oczna
, pp. 89-93
-
-
Arkin, W.1
-
23
-
-
0014902512
-
Rupture of Descemet's membrane in the van der Hoeve-Lobstein syndrome with formation of a keratoschisis
-
Jaeger W Rupture of Descemet's membrane in the van der Hoeve-Lobstein syndrome with formation of a keratoschisis. Ber Zusammenkunft Dtsch Ophthalmol Ges 1970, 639-646.
-
(1970)
Ber Zusammenkunft Dtsch Ophthalmol Ges
, pp. 639-646
-
-
Jaeger, W.1
-
24
-
-
84862886277
-
Descemet stripping automated endothelial keratoplasty for spontaneous descemet membrane detachment in a patient with osteogenesis imperfecta
-
Gorovoy MS, Gorovoy IR, Ullman S, Gorovoy JB Descemet stripping automated endothelial keratoplasty for spontaneous descemet membrane detachment in a patient with osteogenesis imperfecta. Cornea 2012, 832-835.
-
(2012)
Cornea
, pp. 832-835
-
-
Gorovoy, M.S.1
Gorovoy, I.R.2
Ullman, S.3
Gorovoy, J.B.4
-
25
-
-
0021867828
-
The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome
-
Beighton P, Winship I, Behari D The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome. Clin Genet 1985, 69-75.
-
(1985)
Clin Genet
, pp. 69-75
-
-
Beighton, P.1
Winship, I.2
Behari, D.3
-
26
-
-
0029937085
-
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13
-
Gong Y, Vikkula M, Boon L, et al. Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Am J Hum Genet 1996, 59:146-151.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 146-151
-
-
Gong, Y.1
Vikkula, M.2
Boon, L.3
-
27
-
-
18044386744
-
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development
-
Gong Y, Slee RB, Fukai N, et al. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell 2001, 107:513-523.
-
(2001)
Cell
, vol.107
, pp. 513-523
-
-
Gong, Y.1
Slee, R.B.2
Fukai, N.3
-
29
-
-
84865312242
-
Identifying heritable connective tissue disorders in childhood
-
Armon K, Bale P Identifying heritable connective tissue disorders in childhood. Practitioner 2012, 256(1752):19-23.
-
(2012)
Practitioner
, vol.256
, Issue.1752
, pp. 19-23
-
-
Armon, K.1
Bale, P.2
-
30
-
-
0024392153
-
Clinical variability of osteogenesis imperfecta linked to COL1A2 and associated with a structural defect in the type I collagen molecule
-
Superti-Furga A, Pistone F, Romano C, Steinmann B Clinical variability of osteogenesis imperfecta linked to COL1A2 and associated with a structural defect in the type I collagen molecule. J Med Genet 1989, 358-362.
-
(1989)
J Med Genet
, pp. 358-362
-
-
Superti-Furga, A.1
Pistone, F.2
Romano, C.3
Steinmann, B.4
-
31
-
-
77049351232
-
Degenerative state with osteogenesis imperfecta, ichthyosis vulgaris and myopia with nystagmus
-
Ries W Degenerative state with osteogenesis imperfecta, ichthyosis vulgaris and myopia with nystagmus. Dtsch Z Verdau Stoffwechselkr 1951, 11(2-3):96-107.
-
(1951)
Dtsch Z Verdau Stoffwechselkr
, vol.11
, Issue.2-3
, pp. 96-107
-
-
Ries, W.1
-
32
-
-
0034571105
-
The blue sclera syndrome (Van der Heave syndrome)
-
Alikadić-Husović A, Merhemić Z The blue sclera syndrome (Van der Heave syndrome). Med Arh 2000, 54(5-6):325-326.
-
(2000)
Med Arh
, vol.54
, Issue.5-6
, pp. 325-326
-
-
Alikadić-Husović, A.1
Merhemić, Z.2
-
33
-
-
32144434957
-
Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation
-
Nwosu BU, Raygada M, Tsilou ET, Rennert OM, Stratakis CA Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation. Ophthalmic Genet 2005, 135-138.
-
(2005)
Ophthalmic Genet
, pp. 135-138
-
-
Nwosu, B.U.1
Raygada, M.2
Tsilou, E.T.3
Rennert, O.M.4
Stratakis, C.A.5
-
34
-
-
0014504947
-
Lobstein's disease associated with abnormalities of the irido-corneal angle: 3 family cases
-
Bonnet M, Moulin J, Biard L Lobstein's disease associated with abnormalities of the irido-corneal angle: 3 family cases. Bull Soc Ophthalmol Fr 1969, 581-583.
-
(1969)
Bull Soc Ophthalmol Fr
, pp. 581-583
-
-
Bonnet, M.1
Moulin, J.2
Biard, L.3
-
35
-
-
0023183465
-
Hereditary diseases with lens dislocation: clinical aspects
-
Koepp P Hereditary diseases with lens dislocation: clinical aspects. Klin Monatsbl Augenheilkd 1987, 190(1):8-10.
-
(1987)
Klin Monatsbl Augenheilkd
, vol.190
, Issue.1
, pp. 8-10
-
-
Koepp, P.1
-
36
-
-
0042804923
-
Role of the sclera in the development and pathological complications of myopia
-
McBrien NGA Role of the sclera in the development and pathological complications of myopia. Prog Retin Eye Res 2003, 22:307-338.
-
(2003)
Prog Retin Eye Res
, vol.22
, pp. 307-338
-
-
McBrien, N.G.A.1
-
37
-
-
33847709875
-
Progressive myopia due to posterior staphyloma in type I osteogenesis imperfecta
-
Scott A, Kashani S, Towler HMA Progressive myopia due to posterior staphyloma in type I osteogenesis imperfecta. Int Ophthalmol 2005, 167-169.
-
(2005)
Int Ophthalmol
, pp. 167-169
-
-
Scott, A.1
Kashani, S.2
Towler, H.M.A.3
-
40
-
-
0019452222
-
Low ocular rigidity in patients with osteogenesis imperfecta
-
Kaiser-Kupfer MI, McCain L, Shapiro JR, Podgor MJ, Kupfer C, Rowe D Low ocular rigidity in patients with osteogenesis imperfecta. Invest Ophthalmol Vis Sci 1981, 807-809.
-
(1981)
Invest Ophthalmol Vis Sci
, pp. 807-809
-
-
Kaiser-Kupfer, M.I.1
McCain, L.2
Shapiro, J.R.3
Podgor, M.J.4
Kupfer, C.5
Rowe, D.6
-
41
-
-
0021966147
-
Correlation of ocular rigidity and blue sclerae in osteogenesis imperfecta
-
Kaiser-Kupfer MI, Podgor MJ, McCain L, Kupfer C, Shapiro JR Correlation of ocular rigidity and blue sclerae in osteogenesis imperfecta. Trans Ophthalmol Soc UK 1985, 191-195.
-
(1985)
Trans Ophthalmol Soc UK
, pp. 191-195
-
-
Kaiser-Kupfer, M.I.1
Podgor, M.J.2
McCain, L.3
Kupfer, C.4
Shapiro, J.R.5
-
42
-
-
35348841667
-
Traumatic and spontaneous scleral rupture and uveal prolapse in osteogenesis imperfecta
-
Pirouzian A, O'Halloran H, Scher C, Jockin Y, Yaghmai R Traumatic and spontaneous scleral rupture and uveal prolapse in osteogenesis imperfecta. J Pediatr Ophthalmol Strabis 2007, 315-317.
-
(2007)
J Pediatr Ophthalmol Strabis
, pp. 315-317
-
-
Pirouzian, A.1
O'Halloran, H.2
Scher, C.3
Jockin, Y.4
Yaghmai, R.5
-
43
-
-
84878722514
-
Relationship of change in central corneal thickness to visual field progression in eyes with glaucoma
-
Viswanathan D, Goldberg I, Graham SL Relationship of change in central corneal thickness to visual field progression in eyes with glaucoma. Graefes Arch Clin Exp Ophthalmol 2013, 251(6):1593-1599.
-
(2013)
Graefes Arch Clin Exp Ophthalmol
, vol.251
, Issue.6
, pp. 1593-1599
-
-
Viswanathan, D.1
Goldberg, I.2
Graham, S.L.3
-
44
-
-
33646190149
-
Central corneal thickness and corneal hysteresis associated with glaucoma damage
-
Congdon NG, Broman AT, Bandeen-Roche K, Grover D, Quigley HA Central corneal thickness and corneal hysteresis associated with glaucoma damage. Am J Ophthalmol 2006, 868-875.
-
(2006)
Am J Ophthalmol
, pp. 868-875
-
-
Congdon, N.G.1
Broman, A.T.2
Bandeen-Roche, K.3
Grover, D.4
Quigley, H.A.5
-
45
-
-
0017786302
-
Case of Ekman-Lobstein-van der Hoeve syndrome with bilateral glaucoma and right-sided thrombosis of the central retinal vein
-
Smolińska K, Olbromska W Case of Ekman-Lobstein-van der Hoeve syndrome with bilateral glaucoma and right-sided thrombosis of the central retinal vein. Pol Tyg Lek 1977, 843-844.
-
(1977)
Pol Tyg Lek
, pp. 843-844
-
-
Smolińska, K.1
Olbromska, W.2
-
46
-
-
84861191426
-
Osteogenesis imperfecta and glaucoma. A case report
-
Rosbach J, Vossmerbaeumer U, Renieri G, Pfeiffer N, Thieme H Osteogenesis imperfecta and glaucoma. A case report. Ophthalmologe 2012, 479-482.
-
(2012)
Ophthalmologe
, pp. 479-482
-
-
Rosbach, J.1
Vossmerbaeumer, U.2
Renieri, G.3
Pfeiffer, N.4
Thieme, H.5
-
48
-
-
3042584856
-
Optic nerve damage in mice with a targeted type I collagen mutation
-
Mabuchi F, Lindsey JD, Aihara M, Mackey MR, Weinreb RN Optic nerve damage in mice with a targeted type I collagen mutation. Invest Ophthalmol Vis Sci 2004, 1841-1845.
-
(2004)
Invest Ophthalmol Vis Sci
, pp. 1841-1845
-
-
Mabuchi, F.1
Lindsey, J.D.2
Aihara, M.3
Mackey, M.R.4
Weinreb, R.N.5
-
49
-
-
73349127822
-
Outflow facility in mice with a targeted type I collagen mutation
-
Dai YLJ, Duong-Polk X, Nguyen D, Hofer A, Weinreb RN Outflow facility in mice with a targeted type I collagen mutation. Invest Ophthalmol Vis Sci 2009, 50:5749-5753.
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 5749-5753
-
-
Dai, Y.L.J.1
Duong-Polk, X.2
Nguyen, D.3
Hofer, A.4
Weinreb, R.N.5
-
50
-
-
0842331147
-
Corneal thickness: measurement and implications
-
Ehlers N, Hjortdal J Corneal thickness: measurement and implications. Exp Eye Res 2004, 543-548.
-
(2004)
Exp Eye Res
, pp. 543-548
-
-
Ehlers, N.1
Hjortdal, J.2
-
51
-
-
0014449853
-
Intraocular pressure and excretion of mucopolysaccharides in osteogenesis imperfecta
-
Berggren L, Wessler E, Wennerström J Intraocular pressure and excretion of mucopolysaccharides in osteogenesis imperfecta. Acta Ophthalmol 1969, 122-128.
-
(1969)
Acta Ophthalmol
, pp. 122-128
-
-
Berggren, L.1
Wessler, E.2
Wennerström, J.3
-
52
-
-
0020804090
-
Subhyaloid hemorrhage in osteogenesis imperfecta tarda
-
Khalil MK Subhyaloid hemorrhage in osteogenesis imperfecta tarda. Can J Ophthalmol 1983, 251-252.
-
(1983)
Can J Ophthalmol
, pp. 251-252
-
-
Khalil, M.K.1
-
53
-
-
3042660171
-
Retinal hemorrhages in type I osteogenesis imperfecta after minor trauma
-
Ganesh A, Jenny C, Geyer J, Shouldice M, Levin AV Retinal hemorrhages in type I osteogenesis imperfecta after minor trauma. Ophthalmology 2004, 1428-1431.
-
(2004)
Ophthalmology
, pp. 1428-1431
-
-
Ganesh, A.1
Jenny, C.2
Geyer, J.3
Shouldice, M.4
Levin, A.V.5
-
54
-
-
0028048428
-
Retinal detachment in osteogenesis imperfecta
-
Madigan WP, Wertz D, Cockerham GC, Thach AB Retinal detachment in osteogenesis imperfecta. J Pediatr Ophthalmol Strabis 1994, 31(4):268-269.
-
(1994)
J Pediatr Ophthalmol Strabis
, vol.31
, Issue.4
, pp. 268-269
-
-
Madigan, W.P.1
Wertz, D.2
Cockerham, G.C.3
Thach, A.B.4
-
56
-
-
84861325138
-
Intravitreal bevacizumab for treatment of choroidal neovascularization associated with osteogenesis imperfecta
-
Rishi P, Rishi E, Venkatraman A Intravitreal bevacizumab for treatment of choroidal neovascularization associated with osteogenesis imperfecta. Indian J Ophthalmol 2012, 229-231.
-
(2012)
Indian J Ophthalmol
, pp. 229-231
-
-
Rishi, P.1
Rishi, E.2
Venkatraman, A.3
-
57
-
-
84863880691
-
Surgical repair of bilateral full thickness macular holes in a patient with blue sclera secondary to osteogenesis imperfecta
-
Benzimra JD, Kapoor B, Edmeades N, Burger A, Simcock PR Surgical repair of bilateral full thickness macular holes in a patient with blue sclera secondary to osteogenesis imperfecta. Eye 2012, 1023-1024.
-
(2012)
Eye
, pp. 1023-1024
-
-
Benzimra, J.D.1
Kapoor, B.2
Edmeades, N.3
Burger, A.4
Simcock, P.R.5
-
58
-
-
0028343752
-
A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents
-
Al Gazali LI, Sabrinathan K, Nair KG A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents. Clin Dysmorphol 1994, 3(1):55-62.
-
(1994)
Clin Dysmorphol
, vol.3
, Issue.1
, pp. 55-62
-
-
Al Gazali, L.I.1
Sabrinathan, K.2
Nair, K.G.3
-
59
-
-
84902417245
-
Late oto-neuroophthalmological manifestations in a case of osteogenesis imperfecta congenita
-
Arnould G, Dureux JB, Martin JY, Tridon P Late oto-neuroophthalmological manifestations in a case of osteogenesis imperfecta congenita. Rev Otoneuroophthalmol 1957, 405-413.
-
(1957)
Rev Otoneuroophthalmol
, pp. 405-413
-
-
Arnould, G.1
Dureux, J.B.2
Martin, J.Y.3
Tridon, P.4
-
60
-
-
0016375013
-
Optic nerve injury in a patient with osteogenesis imperfecta tarda
-
Gogolkiewicz J Optic nerve injury in a patient with osteogenesis imperfecta tarda. Klin Oczna 1974, 269-272.
-
(1974)
Klin Oczna
, pp. 269-272
-
-
Gogolkiewicz, J.1
-
61
-
-
0023252373
-
Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: a newly recognized type of osteogenesis imperfecta
-
Cole DE, Carpenter TO Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: a newly recognized type of osteogenesis imperfecta. J Pediatr 1987, 76-80.
-
(1987)
J Pediatr
, pp. 76-80
-
-
Cole, D.E.1
Carpenter, T.O.2
-
62
-
-
0018305858
-
Vitreoretinal degeneration as a sign of generalized connective tissue diseases
-
1
-
Maumenee IH Vitreoretinal degeneration as a sign of generalized connective tissue diseases. Am J Ophthalmol 1979, 88(3 Pt 1):432-449.
-
(1979)
Am J Ophthalmol
, vol.88
, Issue.3 PT
, pp. 432-449
-
-
Maumenee, I.H.1
|