Colville D - Search Results

1

Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.

Colville D, Wang YY, Jamieson R, Collins F, Hood J, Savige J. Colville D, et al. Ophthalmic Genet. 2000 Dec;21(4):217-25. Ophthalmic Genet. 2000. PMID: 11135492

2

Albipunctatus retinopathy in inherited interstitial nephritis.

Colville D, Savige J. Colville D, et al. Aust N Z J Ophthalmol. 1994 Nov;22(4):267-9. doi: 10.1111/j.1442-9071.1994.tb00795.x. Aust N Z J Ophthalmol. 1994. PMID: 7727105

3

Ocular abnormalities in thin basement membrane disease.

Colville D, Savige J, Branley P, Wilson D. Colville D, et al. Br J Ophthalmol. 1997 May;81(5):373-7. doi: 10.1136/bjo.81.5.373. Br J Ophthalmol. 1997. PMID: 9227202 Free PMC article.

4

Ocular manifestations of autosomal recessive Alport syndrome.

Colville D, Savige J, Morfis M, Ellis J, Kerr P, Agar J, Fasset R. Colville D, et al. Ophthalmic Genet. 1997 Sep;18(3):119-28. doi: 10.3109/13816819709057125. Ophthalmic Genet. 1997. PMID: 9361309

5

Alport syndrome. A review of the ocular manifestations.

Colville DJ, Savige J. Colville DJ, et al. Ophthalmic Genet. 1997 Dec;18(4):161-73. doi: 10.3109/13816819709041431. Ophthalmic Genet. 1997. PMID: 9457747 Review.

6

Ocular clues to the nature of disease causing end-stage renal failure.

Colville D, Dagher H, Miach P, Savige J. Colville D, et al. Nephrol Dial Transplant. 2000 Mar;15(3):429-32. doi: 10.1093/ndt/15.3.429. Nephrol Dial Transplant. 2000. PMID: 10692536 No abstract available.

7

Ultrastructural appearance of renal and other basement membranes in the Bull terrier model of autosomal dominant hereditary nephritis.

Hood JC, Savige J, Seymour AE, Dowling J, Martinello P, Colville D, Sinclair R, Naito I, Jennings G, Huxtable C. Hood JC, et al. Among authors: colville d. Am J Kidney Dis. 2000 Aug;36(2):378-91. doi: 10.1053/ajkd.2000.8989. Am J Kidney Dis. 2000. PMID: 10922317

8

A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome.

Dagher H, Buzza M, Colville D, Jones C, Powell H, Fassett R, Wilson D, Agar J, Savige J. Dagher H, et al. Among authors: colville d. Am J Kidney Dis. 2001 Dec;38(6):1217-28. doi: 10.1053/ajkd.2001.29217. Am J Kidney Dis. 2001. PMID: 11728953

9

Visual impairment caused by retinal abnormalities in mesangiocapillary (membranoproliferative) glomerulonephritis type II ("dense deposit disease").

Colville D, Guymer R, Sinclair RA, Savige J. Colville D, et al. Am J Kidney Dis. 2003 Aug;42(2):E2-5. doi: 10.1016/s0272-6386(03)00665-6. Am J Kidney Dis. 2003. PMID: 12900843

10

Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.

Shaw EA, Colville D, Wang YY, Zhang KW, Dagher H, Fassett R, Guymer R, Savige J. Shaw EA, et al. Among authors: colville d. Nephrol Dial Transplant. 2007 Jan;22(1):104-8. doi: 10.1093/ndt/gfl607. Epub 2006 Oct 27. Nephrol Dial Transplant. 2007. PMID: 17071739

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