Quantitative optical coherence tomography angiography biomarkers for Alport syndrome

Author:

Cunha Ana MariaORCID,Teixeira Daniela,Cabral Diogo,Estrela-Silva Sérgio,Falcão-Reis Fernando,Carneiro Ângela

Publisher

S. Karger AG

Subject

Sensory Systems,Ophthalmology,General Medicine

Reference24 articles.

1. Alport AC. Hereditary familial congenital haemorrhagic nephritis. Br Med J. 1927;1(3454):504–6.

2. Nagel M, Nagorka S, Gross O. Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome. Hum Mutat. 2005;26:60.

3. Kruegel J, Rubel D, Gross O. Alport syndrome;insights from basic and clinical research. Nat Rev Nephrol. 2013 Mar;9(3):170–8.

4. Kalluri R, Shield CF, Todd P, Hudson BG, Neilson EG. Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis. J Clin Invest. 1997;99:2470–8.

5. Feingold J, Bois E, Chompret A, Broyer M, Gubler MC, Grünfeld JP. Genetic heterogeneity of Alport syndrome. Kidney Int. 1985;27:672–7.

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