ADPKD
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A post hoc analysis of TEMPO 3:4 results examined longer-term effects of tolvaptan on TKV and eGFR in patients with ADPKD.
Data regarding mortality specific to patients with autosomal dominant polycystic kidney disease (ADPKD) are limited.
A team evaluated the Mayo imaging classification system's ability to predict kidney outcomes in an ADPKD cohort.
Researchers compared factors associated with intracranial aneurysm in patients with ADPKD.
The FDA granted orphan drug designation to AP303 for the treatment of autosomal dominant polycystic kidney disease (ADPKD).
Nephrologist Ronald Perrone, MD, has joined the clinical advisory board of XORTX Therapeutics, Inc.
The FDA approved a clinical trial of VX-407 to treat autosomal dominant polycystic kidney disease.
Researchers examined the association between good nutritional status and preservation of kidney function in ADPKD.
Unilateral nephrectomy resulted in a decrease of 46.4% in urinary EGF excretion, and a decrease of 35.2% in eGFR.
Patients with autosomal dominant polycystic kidney disease commonly progress to ESRD in the fifth decade of life.
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the accumulation of fluid-filled cysts in the kidney
Results of a study evaluating the prevalence of common comorbid conditions in patients with ADPKD.
Clinical development models for polycystic kidney disease remain challenging.
Tolvaptan showed real-world effectiveness in slowing decline in eGFR when compared with matched historical controls.
Patients with autosomal dominant polycystic kidney disease commonly develop end-stage kidney disease.
First, an automated kidney volume segmentation model is used to accurately calculate htTKV.
A literature review of possible nonpharmacological therapeutic strategies to slow enlargement of cysts in ADPKD.
The CKiD equation was associated with the highest prevalence of hyperfiltration (35%).
Disease acceptance among patients with autosomal dominant polycystic kidney disease.
Health-related quality of life (HRQoL) is adversely affected in patients with autosomal dominant polycystic kidney ...
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