Liver cysts were found in 46 (29 per cent) of 158 patients over 10 years of age with documented
autosomal dominant-type polycystic kidney disease (PKD) from 62 unrelated families. …

Methods Simultaneous renal clearance of inulin, en-dogenous creatinine, urea nitrogen,'251-iothalamate
and'69YB-DTPA were performed in stable, uremic adult patients in the age …

The improvement of a patient’s facial appearance is one of the main goals of contemporary
orthodontic treatment. The aim of this investigation was to evaluate the difference in facial …

In 259 subjects at risk to have inherited autosomal dominant polycystic kidney disease (PKD),
the frequency of symptoms consistent with urinary tract infection, haematuria, back and …

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, …

The purpose of this study was to define manifestations of autosomal dominant polycystic kidney
disease (ADPKD) in older patients with the disease. Fifty-seven subjects age 50 years or …

Fertility and pregnancy complications were assessed in 137 women at risk of having inherited
the gene for autosomal dominant polycystic kidney disease. Seventy-six (55%) of these …

Percutaneous renal biopsy was performed in a surface coal miner with radiographic and
histopathologic pulmonary changes consistent with acute silicolipoproteinosis who developed …

Orofaciodigital syndrome type I (OFD I) includes striking orodental, facial, digital, renal, and
central nervous system (CNS) abnormalities. Frequently associated with mental retardation, …

BACKGROUND AND PURPOSE: On the basis of limited available data, brain MR imaging
abnormalities in kidney transplant recipients (KTRs) have been predominantly attributed to …