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Cornea

Volumn 30, Issue 3, 2011, Pages 367-370

Corneal clouding in alport syndrome

(4) Herwig, Martina C a Eter, Nicole a Holz, Frank G a Loeffler, Karin U a

a UNIVERSITY OF BONN (Germany)

Author keywords

Alport syndrome; Bowman layer; cornea; histology; lamellar macular hole

Indexed keywords

GLYCOSAMINOGLYCAN;

ADULT; ALPORT SYNDROME; ARTICLE; BOWMAN MEMBRANE; CASE REPORT; CORNEA DYSTROPHY; CORNEA TRANSPLANTATION; ELECTRON MICROSCOPY; ELECTRORETINOGRAPHY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; KERATOPLASTY; KIDNEY FAILURE; MALE; MICROSCOPY; OPTICAL COHERENCE TOMOGRAPHY; POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; RENAL REPLACEMENT THERAPY; RETINA DISEASE; RETINA MACULA HOLE; VISUAL ACUITY;

BOWMAN MEMBRANE; CORNEAL DYSTROPHIES, HEREDITARY; ENDOTHELIUM, CORNEAL; EPITHELIUM, CORNEAL; GLYCOSAMINOGLYCANS; HUMANS; KERATOPLASTY, PENETRATING; KIDNEY TRANSPLANTATION; MALE; MIDDLE AGED; NEPHRITIS, HEREDITARY; VISUAL ACUITY;

EID: 79951770640 PISSN: 02773740 EISSN: None Source Type: Journal
DOI: 10.1097/ICO.0b013e3181eeb0f9 Document Type: Article

Times cited : (11)

References (18)

1
- 84965236793
- Hereditary familial congenital haemorrhagic nephritis
- Alport AC Hereditary familial congenital haemorrhagic nephritis. Br Med J. 1927;1:504-506.
- (1927) Br Med J , vol.1 , pp. 504-506
- Alport, A.C.¹

2
- 0001067060
- Renal disease, inner ear deafness, and ocular changes; A new heredofamilial syndrome
- Sohar E. Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome. AMA Arch Intern Med. 1956;97:627-630.
- (1956) AMA Arch Intern Med , vol.97 , pp. 627-630
- Sohar, E.¹

3
- 0031473018
- Alport syndrome. A review of the ocular manifestations
- Colville DJ, Savige J. Alport syndrome. A review of the ocular manifestations. Ophthalmic Genet. 1997;18:161-173. (Pubitemid 28039523)
- (1997) Ophthalmic Genetics , vol.18 , Issue.4 , pp. 161-173
- Colville, D.J.¹ Savige, J.²

4
- 67650613986
- Novel corneal phenotype in a patient with alport syndrome
- Bower KS, Edwards JD, Wagner ME, et al. Novel corneal phenotype in a patient with alport syndrome. Cornea. 2009;28:599-606.
- (2009) Cornea , vol.28 , pp. 599-606
- Bower, K.S.¹ Edwards, J.D.² Wagner, M.E.³

5
- 59049100882
- ISCEV standard for full-field clinical electroretinography (2008 update)
- Marmor MF, Fulton AB, Holder GE, et al. ISCEV standard for full-field clinical electroretinography (2008 update). Doc Ophthalmol. 2009;118: 69-77.
- (2009) Doc Ophthalmol. , vol.118 , pp. 69-77
- Marmor, M.F.¹ Fulton, A.B.² Holder, G.E.³

6
- 0028971366
- Establishment by the rat lymph node method of epitope-defined monoclonal antibodies recognizing the six different alpha chains of human type IV collagen
- Sado Y, Kagawa M, Kishiro Y, et al. Establishment by the rat lymph node method of epitope-defined monoclonal antibodies recognizing the six different alpha chains of human type IV collagen. Histochem Cell Biol. 1995;104:267-275.
- (1995) Histochem Cell Biol , vol.104 , pp. 267-275
- Sado, Y.¹ Kagawa, M.² Kishiro, Y.³

7
- 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 alpha2 chain oftype VIII collagen, cause two forms ofcorneal endothelial dystrophy Hum Mol Genet. 2001;10:2415-2423. (Pubitemid 33069547)
- (2001) Human Molecular Genetics , vol.10 , Issue.21 , pp. 2415-2423
- Biswas, S.¹ Munier, F.L.² Yardley, J.³ Hart-Holden, N.⁴ Perveen, R.⁵ Cousin, P.⁶ Sutphin, J.E.⁷ Noble, B.⁸ Batterbury, M.⁹ Kielty, C.¹⁰ Hackett, A.¹¹ Bonshek, R.¹² Ridgway, A.¹³ McLeod, D.¹⁴ Sheffield, V.C.¹⁵ Stone, E.M.¹⁶ Schorderet, D.F.¹⁷ Black, G.C.M.¹⁸

8
- 27244444742
- Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells
- DOI 10.1086/497348
- 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. (Pubitemid 41513274)
- (2005) American Journal of Human Genetics , vol.77 , Issue.5 , pp. 694-708
- Krafchak, C.M.¹ Pawar, H.² Moroi, S.E.³ Sugar, A.⁴ Lichter, P.R.⁵ Mackey, D.A.⁶ Mian, S.⁷ Nairus, T.⁸ Elner, V.⁹ Schteingart, M.T.¹⁰ Downs, C.A.¹¹ Kijek, T.G.¹² Johnson, J.M.¹³ Trager, E.H.¹⁴ Rozsa, F.W.¹⁵ Mandal, N.A.¹⁶ Epstein, M.P.¹⁷ Vollrath, D.¹⁸ Ayyagari, R.¹⁹ Boehnke, M.²⁰ Richards, J.E.²¹ more..

9
- 67349251191
- Changes in the localization of collagens IV and VIII in corneas obtained from patients with posterior polymorphous corneal dystrophy
- Merjava S, Liskova P, Sado Y, et al. Changes in the localization of collagens IV and VIII in corneas obtained from patients with posterior polymorphous corneal dystrophy. Exp Eye Res. 2009;88:945-952.
- (2009) Exp Eye Res , vol.88 , pp. 945-952
- Merjava, S.¹ Liskova, P.² Sado, Y.³

10
- 38449103731
- Compositional differences between infant and adult human corneal basement membranes
- DOI 10.1167/iovs.07-0654
- Kabosova A, Azar DT, Bannikov GA, et al. Compositional differences between infant and adult human corneal basement membranes. Invest Ophthalmol Vis Sci. 2007;48:4989-4999. (Pubitemid 351260908)
- (2007) Investigative Ophthalmology and Visual Science , vol.48 , Issue.11 , pp. 4989-4999
- Kabosova, A.¹ Azar, D.T.² Bannikov, G.A.³ Campbell, K.P.⁴ Durbeej, M.⁵ Ghohestani, R.F.⁶ Jones, J.C.R.⁷ Kenney, M.C.⁸ Koch, M.⁹ Ninomiya, Y.¹⁰ Patton, B.L.¹¹ Paulsson, M.¹² Sado, Y.¹³ Sage, E.H.¹⁴ Sasaki, T.¹⁵ Sorokin, L.M.¹⁶ Steiner-Champliaud, M.-F.¹⁷ Sun, T.-T.¹⁸ SundarRaj, N.¹⁹ Timpl, R.²⁰ Virtanen, I.²¹ Ljubimov, A.V.²² more..

11
- 0016704326
- Corneal clouding with increased acid mucopolysaccharide accumulation in Bowman's membrane
- Rodrigues MM, Calhoun J, Harley RD. Corneal clouding with increased acid mucopolysaccharide accumulation in Bowman's membrane. Am J Ophthalmol. 1975;79:916-924.
- (1975) Am J Ophthalmol , vol.79 , pp. 916-924
- Rodrigues, M.M.¹ Calhoun, J.² Harley, R.D.³

12
- 0015470999
- Corneal mucopolysaccharidosis. Light and electron microscopic study of an atypical case after keratoplasty
- Edmison DR, Robertson DM, Rosen DA. Corneal mucopolysacchar-idosis. Light and electron microscopic study of an atypical case after keratoplasty. Can J Ophthalmol. 1972;7:271-279.
- (1972) Can J Ophthalmol , vol.7 , pp. 271-279
- Edmison, D.R.¹ Robertson, D.M.² Rosen, D.A.³

13
- 0027481419
- Diffuse corneal clouding in siblings with fetal alcohol syndrome
- Edward DP, Li J, Sawaguchi S, et al. Diffuse corneal clouding in siblings with fetal alcohol syndrome. Am J Ophthalmol. 1993;115:484-493. (Pubitemid 23109801)
- (1993) American Journal of Ophthalmology , vol.115 , Issue.4 , pp. 484-493
- Edward, D.P.¹ Li, J.² Sawaguchi, S.³ Sugar, J.⁴ Yue, B.Y.J.T.⁵ Tso, M.O.M.⁶

14
- 0023630859
- ANGEBORENE HORNHAUTTRUBUNG DURCH VERDICKUNG DER BOWMANSCHEN MEMBRAN
- Ohrloff C, Olson R, Apple D. [Congenital corneal opacity caused by thickening ofBowman's membrane]. Klin Monbl Augenheilkd. 1987;191: 352-354. (Pubitemid 17165317)
- (1987) Klinische Monatsblatter fur Augenheilkunde , vol.191 , Issue.5 , pp. 352-354
- Ohrloff, C.¹ Olson, R.² Apple, D.³

15
- 0021205752
- Congenital corneal opacification secondary to Bowman's layer dysgenesis
- Apple DJ, Olson RJ, Jones GR, et al. Congenital corneal opacification secondary to Bowman's layer dysgenesis. Am J Ophthalmol. 1984;98: 320-328. (Pubitemid 14030673)
- (1984) American Journal of Ophthalmology , vol.98 , Issue.3 , pp. 320-328
- Apple, D.J.¹ Olson, R.J.² Jones, G.R.³

16
- 0036672019
- Bilateral macular holes: An unusual feature of Alport syndrome
- Gupta V, Kumar N. Bilateral macular holes: an unusual feature ofalport syndrome. Retina. 2002;22:499-501. (Pubitemid 35025530)
- (2002) Retina , vol.22 , Issue.4 , pp. 499-501
- Gupta, V.¹ Kumar, N.²

17
- 0029975894
- Alport's syndrome with bilateral macular hole
- Mete UO, Karaaslan C, Ozbilgin MK, et al. Alport's syndrome with bilateral macular hole. Acta Ophthalmol Scand. 1996;74:77-80. (Pubitemid 26093806)
- (1996) Acta Ophthalmologica Scandinavica , vol.74 , Issue.1 , pp. 77-80
- Mete, U.O.¹ Karaaslan, C.² Ozbilgin, M.K.³ Polat, S.⁴ Tap, O.⁵ Kaya, M.⁶

18
- 34248181564
- Giant macular hole in Alport syndrome
- DOI 10.3129/can.j.ophthalmol.i07-020
- Rahman W, Banerjee S. Giant macular hole in Alport syndrome. Can J Ophthalmol. 2007;42:314-315. (Pubitemid 46713692)
- (2007) Canadian Journal of Ophthalmology , vol.42 , Issue.2 , pp. 314-315
- Rahman, W.¹ Banerjee, S.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.