Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutations

Author:

Stock Johanna,Kuenanz Johannes,Glonke Niklas,Sonntag Joseph,Frese Jenny,Tönshoff Burkhard,Höcker Britta,Hoppe Bernd,Feldkötter Markus,Pape Lars,Lerch Christian,Wygoda Simone,Weber Manfred,Müller Gerhard-Anton,Gross Oliver

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Reference29 articles.

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2. Krügel J, Rubel D, Gross O (2013) Alport syndrome—Recent insights in basic and clinical research. Nat Rev Nephrol 9(3):170–178

3. Hertz JM, Thomassen M, Storey H, Flinter F (2015) Clinical utility gene card for: Alport syndrome—update 2014. Eur J Hum Genet 23(9). doi: 10.1038/ejhg.2014.254

4. Storey H, Savige J, Sivakumar V, Abbs S, Flinter FA (2013) COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome. J Am Soc Nephrol 24(12):1945–1954

5. Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer K-O, Flinter F, Pirson Y, Verellen C, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Krejcova S, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC (2000) X-linked Alport syndrome: natural history in 195 families and genotype–phenotype correlations in males. J Am Soc Nephrol 11:649–657

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