Ridgway AE - Search Results

1

Granular corneal dystrophy Groenouw type I. A report of a probable homozygous patient.

Møller HU, Ridgway AE. Møller HU, et al. Among authors: ridgway ae. Acta Ophthalmol (Copenh). 1990 Feb;68(1):97-101. doi: 10.1111/j.1755-3768.1990.tb01658.x. Acta Ophthalmol (Copenh). 1990. PMID: 2336942

2

Differential diagnosis between granular corneal dystrophy Groenouw type I and paraproteinemic crystalline keratopathy.

Møller HU, Ehlers N, Bojsen-Møller M, Ridgway AE. Møller HU, et al. Among authors: ridgway ae. Acta Ophthalmol (Copenh). 1993 Aug;71(4):552-5. doi: 10.1111/j.1755-3768.1993.tb04635.x. Acta Ophthalmol (Copenh). 1993. PMID: 8249591

3

Genetics of granular dystrophy.

Ridgway AE, Moller HU. Ridgway AE, et al. Ophthalmology. 1992 Dec;99(12):1753. doi: 10.1016/s0161-6420(92)31728-2. Ophthalmology. 1992. PMID: 1480387 No abstract available.

4

Lectin binding sites in normal, scarred, and lattice dystrophy corneas.

Bishop PN, Bonshek RE, Jones CJ, Ridgway AE, Stoddart RW. Bishop PN, et al. Among authors: ridgway ae. Br J Ophthalmol. 1991 Jan;75(1):22-7. doi: 10.1136/bjo.75.1.22. Br J Ophthalmol. 1991. PMID: 1703789 Free PMC article.

5

Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?

Ridgway AE, Akhtar S, Munier FL, Schorderet DF, Stewart H, Perveen R, Bonshek RE, Odenthal MT, Dixon M, Barraquer R, Escoto R, Black GC. Ridgway AE, et al. Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3286-92. Invest Ophthalmol Vis Sci. 2000. PMID: 11006215

6

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

Biswas S, Munier FL, Yardley J, Hart-Holden N, Perveen R, Cousin P, Sutphin JE, Noble B, Batterbury M, Kielty C, Hackett A, Bonshek R, Ridgway A, McLeod D, Sheffield VC, Stone EM, Schorderet DF, Black GC. Biswas S, et al. Hum Mol Genet. 2001 Oct 1;10(21):2415-23. doi: 10.1093/hmg/10.21.2415. Hum Mol Genet. 2001. PMID: 11689488

7

Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.

Stewart HS, Parveen R, Ridgway AE, Bonshek R, Black GC. Stewart HS, et al. Among authors: ridgway ae. Br J Ophthalmol. 2000 Apr;84(4):390-4. doi: 10.1136/bjo.84.4.390. Br J Ophthalmol. 2000. PMID: 10729296 Free PMC article.

8

Deposits and proteoglycan changes in primary and recurrent granular dystrophy of the cornea.

Akhtar S, Meek KM, Ridgway AE, Bonshek RE, Bron AJ. Akhtar S, et al. Among authors: ridgway ae. Arch Ophthalmol. 1999 Mar;117(3):310-21. doi: 10.1001/archopht.117.3.310. Arch Ophthalmol. 1999. PMID: 10088808

9

Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis.

Stewart HS, Ridgway AE, Dixon MJ, Bonshek R, Parveen R, Black G. Stewart HS, et al. Among authors: ridgway ae. Hum Mutat. 1999;14(2):126-32. doi: 10.1002/(SICI)1098-1004(1999)14:2<126::AID-HUMU4>3.0.CO;2-W. Hum Mutat. 1999. PMID: 10425035

10

Superficial granular corneal dystrophy with amyloid deposits.

Ridgway AE. Ridgway AE. Arch Ophthalmol. 1993 Jul;111(7):901. doi: 10.1001/archopht.1993.01090070019006. Arch Ophthalmol. 1993. PMID: 8328927 No abstract available.

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