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Australian and New Zealand Journal of Ophthalmology|November 1, 1994
Albipunctatus retinopathy in inherited interstitial nephritisD Colville, J SavigeThe British Journal of Ophthalmology|May 1, 1997
Ocular abnormalities in thin basement membrane diseaseD Colville, J Savige, P Branley, et al.The British Journal of Ophthalmology|November 21, 2008
The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failureD Colville, Y Y Wang, R Tan, et al.Journal of the American Society of Nephrology : JASN|January 24, 1998
Early nephropathy predicts vision-threatening retinal disease in patients with type I diabetes mellitusR E Gilbert, C Tsalamandris, T J Allen, et al.American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|November 30, 2013
Diagnostic accuracy of impression-free digital modelsSercan Akyalcin, Benjamin E Cozad, Jeryl D English, et al.Ophthalmic Genetics|January 3, 2001
Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormaltiesD Colville, Y Y Wang, R Jamieson, et al.Ophthalmic Genetics|November 15, 1997
Ocular manifestations of autosomal recessive Alport syndromeD Colville, J Savige, M Morfis, et al.The British Journal of Ophthalmology|November 21, 2008
The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphismsJ Liu, D Colville, Y Y Wang, et al.Scientific Reports|May 17, 2022
Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesisP Harraka, H Mack, D Colville, et al.Scientific Reports|July 11, 2022
Retinal drusen counts are increased in inflammatory bowel disease, and with longer disease duration, more complications and associated IgA glomerulonephritisE Nicklason, Y Ham, D Ng, et al.Pageof 2