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Polycystic Kidney, Autosomal Dominant

Known as: Polycystic Kidney Disease, Autosomal Dominant, ADPKD, Polycystic Kidney, Autosomal Dominant [Disease/Finding] 
Polycystic kidney disease inherited in an autosomal dominant pattern. Symptoms usually appear at middle age and include abdominal pain, hematuria and… 
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Genetic testing of PKD1 and PKD2 is useful for diagnosis and prognosis of autosomal dominant polycystic kidney disease (ADPKD… 
2007
2007
Background: In young ADPKD patients, we have previously found an impaired endothelium-dependent relaxation in small resistance… 
Review
2006
Review
2006
Autosomal recessive polycystic kidney disease (ARPKD) belongs to a group of congenital hepatorenal fibrocystic syndromes… 
Review
2006
Review
2006
For more than three decades, autosomal dominant polycytic kidney disease (ADPKD) researchers around the globe, spurned by… 
Review
2006
Review
2006
Autosomal dominant polycystic kidney disease (ADPKD) is one of the commonest inherited human disorders yet remains relatively… 
Review
2001
Review
2001
Data from animal and human studies suggest that the rate of progression of renal insufficiency can be retarded with careful… 
Highly Cited
1999
Highly Cited
1999
ABSTRACT Autosomal dominant polycystic kidney disease (ADPKD) is caused by germ line mutations in at least three ADPKD genes. Two… 
Highly Cited
1999
Highly Cited
1999
It is estimated that approximately 15% of families with autosomal dominant polycystic kidney disease (ADPKD) have mutations in… 
1990
1990
High resolution computed tomography or magnetic resonance imaging of the head with 3-mm sections through the circle of Willis was…