Autosomal dominant polycystic kidney disease (ADPKD) is generally a late-onset
multisystem disorder characterized by bilateral kidney cysts, liver cysts, and an increased …

AB CHAPMAN, and PA GABOW,“HYPERTENSION IN AUTOSOMAL DOMINANT
POLYCYSTIC KIDNEY DISEASE,” KIDNEY INTERNATIONAL (SUPPLEMENT), vol. 61, no …

Linkage analysis was performed on 49 Catalan families with autosomal dominant polycystic
kidney disease obtained via the Nephrology Department and related nephrology centers. A …

The clinical features of 55 cases of autosomal recessive polycystic kidney disease
(ARPCKD) have been reviewed. Each had evidence of ARPCKD. The outcomes of 87 …

▪ Abstract Autosomal dominant polycystic kidney disease (ADPKD) is a common and
systemic disease characterized by formation of focal cysts. Of the three potential causes of …

Collated in this highly personal commentary are the most important research findings of the
past 10 years that deal primarily with the renal manifestations of inherited polycystic kidney …

Although asymptomatic in most patients, extrarenal manifestations of ADPKD may become
more clinically relevant with the increasing life expectancy of affected patients. They mainly …

Results TKV increased from year to year, whereas GFR uncorrected for body surface area
(BSA) decreased only at year 6. Higher lnTKV and urine sodium excretion (U Na V), lower …

It has been suggested that the clinical expression of autosomal dominant polycystic kidney
disease (ADPKD) is uniform among individuals of a given family. To test this hypothesis …

Autosomal dominant polycystic kidney disease has been shown to be closely linked to the
alpha-hemoglobin complex on the short arm of chromosome 16. We describe a five …