Macropuncture study of polycystic disease in adult human kidneys. Solute composition, volume, and hydrostatic pressure were measured in cysts from eight patients with the adult form of polycystic kidney disease (PCKD). Five azotemic patients had elective nephrectomies in preparation for renal transplantation, two nonazotemic patients had their polycystic kidneys removed several weeks after a successful renal allograft, and one nonazotemic cadaver was inadvertently nephrectomized as a potential kidney donor. In all patients, the pattern of solute concentrations in cyst fluid segregated into two principal groups: Proximal cysts had sodium, potassium, chloride, hydrogen ion, creatinine, and urea values virtually equal to their respective sera,...
Rate of functional deterioration in polycystic kidney disease. Renal function was evaluated in 44 pa...
Renal structure in early autosomal-dominant polycystic kidney disease (ADPKD): The Consortium for Ra...
Background and objectives In autosomal dominant polycystic kidney disease, progressive renal enlarge...
Ultrastructure and function of cysts from human adult polycystic kidneys. Twenty cysts from five pat...
Adult polycystic kidney disease: Studies of the defect in urine concentration. Patients with adult p...
Renal cyst epithelial transport in non-uremic polycystic kidney disease. Renal cyst epithelial trans...
poster abstractAutosomal dominant polycystic kidney disease (ADPKD) is characterized by the slow gro...
Renal excretion and cyst accumulation of β2microglobulin in polycystic kidney disease. To determine ...
Polycystic kidney disease (PKD) is characterized by the slow growth of fluid-filled cysts in kidney ...
The clinical utility of renal concentrating capacity in polycystic kidney disease. We studied 177 ad...
On the probability that kidneys are different in autosomal dominant polycystic disease. We hypothesi...
Polycystic kidney diseases (PKD) are genetic disorders characterized by fluid filled cysts in the ki...
Polypoid and papillary epithelial hyperplasia: A potential cause of ductal obstruction in adult poly...
Macropuncture study of polycystic disease in adult human kidneys. Solute composition, volume, and hy...
The progressive formation of single or multiple cysts accompanies several renal diseases. Specifical...
Rate of functional deterioration in polycystic kidney disease. Renal function was evaluated in 44 pa...
Renal structure in early autosomal-dominant polycystic kidney disease (ADPKD): The Consortium for Ra...
Background and objectives In autosomal dominant polycystic kidney disease, progressive renal enlarge...
Ultrastructure and function of cysts from human adult polycystic kidneys. Twenty cysts from five pat...
Adult polycystic kidney disease: Studies of the defect in urine concentration. Patients with adult p...
Renal cyst epithelial transport in non-uremic polycystic kidney disease. Renal cyst epithelial trans...
poster abstractAutosomal dominant polycystic kidney disease (ADPKD) is characterized by the slow gro...
Renal excretion and cyst accumulation of β2microglobulin in polycystic kidney disease. To determine ...
Polycystic kidney disease (PKD) is characterized by the slow growth of fluid-filled cysts in kidney ...
The clinical utility of renal concentrating capacity in polycystic kidney disease. We studied 177 ad...
On the probability that kidneys are different in autosomal dominant polycystic disease. We hypothesi...
Polycystic kidney diseases (PKD) are genetic disorders characterized by fluid filled cysts in the ki...
Polypoid and papillary epithelial hyperplasia: A potential cause of ductal obstruction in adult poly...
Macropuncture study of polycystic disease in adult human kidneys. Solute composition, volume, and hy...
The progressive formation of single or multiple cysts accompanies several renal diseases. Specifical...
Rate of functional deterioration in polycystic kidney disease. Renal function was evaluated in 44 pa...
Renal structure in early autosomal-dominant polycystic kidney disease (ADPKD): The Consortium for Ra...
Background and objectives In autosomal dominant polycystic kidney disease, progressive renal enlarge...