Mass effect from polycystic kidney and liver enlargement can result in significant clinical com-plications and symptoms in autosomal dominant polycystic kidney disease (ADPKD). In this single-center study, we examined the correlation of height-adjusted total liver volume (htTLV) and total kidney volume (htTKV) by CT imaging with hepatic complications (n = 461) and abdominal symptoms (n = 253) in patients with ADPKD. “Mass-effect ” complications were assessed by review of medical records and abdominal symptoms, by a standardized research questionnaire. Overall, 91.8 % of patients had 4 or more liver cysts on CT scans. Polycystic liver disease (PLD) was classified as none or mild (htTLV < 1,600 mL/m); moder-ate (1,600 htTLV <3,200mL/m)...
OBJECTIVE: Autosomal dominant polycystic kidney disease (ADPKD) is a relentlessly progressing form o...
Contains fulltext : 47573.pdf (publisher's version ) (Open Access)Polycystic liver...
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the deve...
Item does not contain fulltextBACKGROUND: There is an ongoing debate if and how kidney and liver vol...
Although polycystic liver disease (PCLD) is one of the extrarenal complications in patients with aut...
Background: There is an ongoing debate if and how kidney and liver volume are associated with pain a...
This article is distributed under the terms of the Creative Commons Attribution 4.0 International Li...
IntroductionAlthough polycystic liver disease (PCLD) is one of the extrarenal complications in patie...
BACKGROUND & AIMS: Polycystic liver disease (PLD) occurs in two genetic disorders, autosomal-dominan...
Autosomal dominant polycystic kidney disease (ADPKD) in humans is characterized by a chronic, slowly...
Contains fulltext : 136540.pdf (publisher's version ) (Open Access)Polycystic live...
Autosomal dominant polycystic kidney disease (ADPKD) in humans is characterized by a chronic, slowly...
Autosomal dominant polycystic kidney disease (PKD) is a hereditary condition characterized by the pr...
HALT PKD consists of two ongoing randomized trials with the largest cohort of systematically studied...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney...
OBJECTIVE: Autosomal dominant polycystic kidney disease (ADPKD) is a relentlessly progressing form o...
Contains fulltext : 47573.pdf (publisher's version ) (Open Access)Polycystic liver...
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the deve...
Item does not contain fulltextBACKGROUND: There is an ongoing debate if and how kidney and liver vol...
Although polycystic liver disease (PCLD) is one of the extrarenal complications in patients with aut...
Background: There is an ongoing debate if and how kidney and liver volume are associated with pain a...
This article is distributed under the terms of the Creative Commons Attribution 4.0 International Li...
IntroductionAlthough polycystic liver disease (PCLD) is one of the extrarenal complications in patie...
BACKGROUND & AIMS: Polycystic liver disease (PLD) occurs in two genetic disorders, autosomal-dominan...
Autosomal dominant polycystic kidney disease (ADPKD) in humans is characterized by a chronic, slowly...
Contains fulltext : 136540.pdf (publisher's version ) (Open Access)Polycystic live...
Autosomal dominant polycystic kidney disease (ADPKD) in humans is characterized by a chronic, slowly...
Autosomal dominant polycystic kidney disease (PKD) is a hereditary condition characterized by the pr...
HALT PKD consists of two ongoing randomized trials with the largest cohort of systematically studied...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney...
OBJECTIVE: Autosomal dominant polycystic kidney disease (ADPKD) is a relentlessly progressing form o...
Contains fulltext : 47573.pdf (publisher's version ) (Open Access)Polycystic liver...
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the deve...