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 …

Autosomal-dominant polycystic kidney disease (ADPKD) affects up to 12 million individuals
and is the fourth most common cause for renal replacement therapy worldwide. There have …

Microbial contamination of the liver parenchyma leading to hepatic abscess (HA) can occur
via the bile ducts or vessels (arterial or portal) or directly, by contiguity. Infection is usually …

Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the
intrahepatic biliary tree. The phenotype consists of numerous cysts spread throughout the …

Complicated Urinary Tract Infections - Abstract - Europe PMC Sign in | Create an account
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Autosomal-dominant polycystic kidney disease (ADPKD) is a systemic disease, marked by
progressive increase of bilateral renal cysts, resulting in chronic kidney disease (CKD) and …

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent cause of
genetic renal disease and accounts for 6–10% of patients on renal replacement therapy …

In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for
kidney transplantation, issues related to native nephrectomy, cystic liver involvement …

Cyst infection is a severe complication of renal and hepatic cystic disease that frequently
leads to hospitalization. In most cases the diagnosis of cyst infection is made empirically as …

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