Risk factors for progression in ADPKD
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Nephrology,Internal Medicine
Reference36 articles.
1. Comparison of phenotypes of polycystic kidney disease types 1 and 2
2. Volume Progression in Autosomal Dominant Polycystic Kidney Disease: The Major Factor Determining Clinical Outcomes
3. Health-Related Quality of Life in Patients With Autosomal Dominant Polycystic Kidney Disease and CKD Stages 1-4: A Cross-sectional Study
4. Type of PKD1 Mutation Influences Renal Outcome in ADPKD
5. Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease
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1. Acyl-CoA thioesterase 13 (ACOT13) attenuates the progression of autosomal dominant polycystic kidney disease in vitro via triggering mitochondrial-related cell apoptosis;Aging;2024-08-21
2. Autosomal Dominant Polycystic Kidney Disease: Epidemiological, Clinical Aspects and Predictive Factors of Poor Renal Prognosis (About 300 Cases);Open Journal of Nephrology;2024
3. CLINICAL AND PROGNOSTIC VALUE OF PROTEOLYSIS FACTORS IN CHILDREN WITH AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE;Nephrology (Saint-Petersburg);2019-02-21
4. Total kidney volume: the most valuable predictor of autosomal dominant polycystic kidney disease progression;Kidney International;2018-03
5. Assessing Risk of Disease Progression and Pharmacological Management of Autosomal Dominant Polycystic Kidney Disease;Canadian Journal of Kidney Health and Disease;2017-01
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