Proteinuria in children with autosomal dominant polycystic kidney disease
Author:
Publisher
Edizioni Minerva Medica
Subject
Pediatrics, Perinatology, and Child Health
Link
https://www.minervamedica.it/pdf.php?cod=R15Y2018N05A0413
Reference24 articles.
1. Overt proteinuria and microalbuminuria in autosomal dominant polycystic kidney disease;Chapman AB;J Am Soc Nephrol,1994
2. Factors relating to urinary protein excretion in children with autosomal dominant polycystic kidney disease;Sharp C;J Am Soc Nephrol,1998
3. Predictors of Autosomal Dominant Polycystic Kidney Disease Progression
4. Autosomal Dominant Polycystic Kidney Disease – Clinical and Genetic Aspects
5. Association of Urinary Biomarkers With Disease Severity in Patients With Autosomal Dominant Polycystic Kidney Disease: A Cross-sectional Analysis
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1. The Impact of Autosomal Dominant Polycystic Kidney Disease in Children: A Nephrological, Nutritional, and Psychological Point of View;Biomedicines;2024-08-12
2. Clinical findings, underlying pathogenetic processes and treatment of vascular dysfunction in autosomal dominant polycystic kidney disease;Renal Failure;2023-11-16
3. Tolvaptan for Children and Adolescents with Autosomal Dominant Polycystic Kidney Disease;Clinical Journal of the American Society of Nephrology;2023-01
4. Autosomal dominant polycystic kidney disease in young adults;Clinical Kidney Journal;2022-11-29
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