Add to ORKGAutosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple macroscopic liver and kidney cysts. Isolated Liver transplantation or combined with kidney is a treatment option for these patients with regards to complications arising in hepatic and kidney cysts that are not controlled by other procedure
Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepa...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney...
Polycystic liver disease (PLD) is arbitrarily defined as a liver that contains >20 cysts. The condit...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
Polycystic disease causes a progressive decrease in renal function and liver degeneration. The progr...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Polycystic liver disease (PLD) is a hereditary disease inherited by autosomal dominant trait that oc...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
International audienceBackground and objectives. In contrast to the improvement in our understanding...
Liver cysts are a commonly encountered phenomenon and may represent a broad cluster of disorders of ...
These guidelines address management of patients with autosomal dominant polycystic kidney disease wh...
Acute or chronic liver failure is commonly associated with some degree of renal dysfunction. In sele...
These guidelines address the management of patients with autosomal dominant polycystic kidney diseas...
Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepa...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney...
Polycystic liver disease (PLD) is arbitrarily defined as a liver that contains >20 cysts. The condit...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
Polycystic disease causes a progressive decrease in renal function and liver degeneration. The progr...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Polycystic liver disease (PLD) is a hereditary disease inherited by autosomal dominant trait that oc...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
International audienceBackground and objectives. In contrast to the improvement in our understanding...
Liver cysts are a commonly encountered phenomenon and may represent a broad cluster of disorders of ...
These guidelines address management of patients with autosomal dominant polycystic kidney disease wh...
Acute or chronic liver failure is commonly associated with some degree of renal dysfunction. In sele...
These guidelines address the management of patients with autosomal dominant polycystic kidney diseas...
Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the intrahepa...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney...
Polycystic liver disease (PLD) is arbitrarily defined as a liver that contains >20 cysts. The condit...