Cystic kidneys are common causes of end-stage renal disease, both in children and in
adults. Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive …

These recommendations were systematically developed on behalf of the Network for Early
Onset Cystic Kidney Disease (NEOCYST) by an international group of experts in autosomal …

The natural history of autosomal dominant polycystic kidney disease (ADPKD) is
characterized by a variable rate of cyst development and increase in total kidney volume …

Purpose of review: Infections are a major contributor to morbidity and mortality in end-stage
renal disease (ESRD) patients. A better understanding of the interplay between infectious …

Context This paper provides a brief overview of urinary tract infections (UTIs) in
immunocompromised patients from the perspective of a practicing urologist. Objective The …

Positron emission tomography combined with computed tomography (PET/CT) is a nuclear
imaging technique which is increasingly being used in infectious diseases. Because …

Autosomal dominant polycystic kidney disease (ADPKD) is a chronic, progressive condition
characterized by the development and growth of cysts in the kidneys and other organs and …

Cyst infection is a frequent and serious complication of autosomal dominant polycystic
kidney disease (ADPKD) that is often difficult to treat and can be fatal. However, much is still …

Introduction Cyst infection is a known complication of autosomal dominant polycystic kidney
disease (ADPKD). Here, we describe incidence, risk factors, clinical presentation, and …

Autosomal dominant polycystic kidney disease (ADPKD) affects up to 1 in 1000 people. The
disease is characterized by the progressive development of cysts throughout the renal …