Macular Lesions in Alport's Disease
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference13 articles.
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2. Hereditary familial congenital haemorrhagic nephritis;Alport;Br. Med. J.,1927
3. Renal disease, inner ear deafness and ocular changes. A new heredofamilial syndrome;Sohar;Arch. Intern. Med.,1956
4. Néphropathie chronique héréditaire avec surdité et atteinte oculaire;Hauser;Schweiz. Med. Wschr.,1974
5. The hereditary renal diseases;Perkoff;N. Engl. J. Med.,1967
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2. Syndrome d’Alport : néphropathie héréditaire associée à des mutations dans les gènes codant les chaînes de collagène de type IV;Néphrologie & Thérapeutique;2016-12
3. Temporal Macular Thinning Associated With X-Linked Alport Syndrome;JAMA Ophthalmology;2013-06-01
4. Retinal Basement Membrane Abnormalities and the Retinopathy of Alport Syndrome;Investigative Opthalmology & Visual Science;2010-03-01
5. Evaluation of Anterior Lenticonus in Alport Syndrome Using Tracey Wavefront Aberrometry and Transmission Electron Microscopy;Ophthalmic Surgery, Lasers and Imaging Retina;2010-01
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