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Letter to the Editor

Response to letter to the editor: therapeutic importance of proteinuria classification in children with congenital anomalies of the kidney and urinary tract

, , , , &
Pages 113-114 | Received 28 Nov 2023, Accepted 11 Dec 2023, Published online: 18 Dec 2023

References

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  • Rivetti G, Gizzone P, Di Sessa A, et al. Renin angiotensin aldosterone inhibitors in the treatment of proteinuria in children with congenital anomalies of the kidney and urinary tract: more evidence needed. Expert Rev Clin Pharmacol. 2023;16(9):791–798. doi: 10.1080/17512433.2023.2247985
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  • Simões Silva A C, Lanza K, Andrade Palmeira V, et al. 2020 update on the renin–angiotensin–aldosterone system in pediatric kidney disease and its interactions with coronavirus. Pediatr Nephrol. 2021;36(6):1407–1426. doi: 10.1007/s00467-020-04759-1/Published
  • Mastrangelo A, Brambilla M, Romano G, et al. Single, double and triple blockade of RAAS in Alport syndrome: different tools to freeze the evolution of the disease. J Clin Med. 2021;10(21):4946. doi: 10.3390/JCM10214946
  • Lubrano R, Soscia F, Elli M, et al. Renal and cardiovascular effects of angiotensin-converting enzyme inhibitor plus angiotensin II receptor antagonist therapy in children with proteinuria. Pediatrics. 2006;118(3):e833–e838. doi: 10.1542/PEDS.2005-2053

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