AbstractBackgroundThe purpose of this study was to determine peri‐operative mortality and long‐term outcomes in patients undergoing liver transplantation in the US using the United Network for Organ Sharing (UNOS) database.MethodsThis study is a retrospective review of liver transplantations (LT) recorded in the UNOS database performed between 1988 and 2010. In total, 107 411 LT were performed in the US, 357 (0.3%) were for adult polycystic liver disease (PLD). A random group of 9416 adult patients transplanted for other diagnoses was created for comparison (10% of the adult non‐PLD database).ResultsTwo hundred and seventy‐one patients in the adult PLD group were females (75.9%), the mean age was 52.3 ± 8.2 [standard deviation (SD)] years. ...
ObjectiveTo analyze a 28-year single-center experience with orthotopic liver transplantation (OLT) f...
AbstractBackgroundThe Model for End‐stage Liver Disease (MELD) has been used as a prognostic tool si...
Introduction: Massive handicapping hepatomegaly due to PLD is accepted as indication for LT. In the ...
AbstractBackgroundThe purpose of this study was to determine peri‐operative mortality and long‐term ...
Polycystic liver disease (PLD) is a celiopathy characterized by progressive growth of multiple hepat...
Introduction Liver transplantation is the only curative option for patients with polycystic liver...
Introduction: Polycystic liver disease (PCLD) occurs either in an isolated form (Autosomal Dominant ...
OBJECTIVE: In an attempt to refine the indications for liver resection (LR) for highly symptomatic p...
AbstractBackground: Liver transplantation (LT) for polycystic liver disease (PLD) has evolved to be ...
Polycystic liver disease (PLD) may provoke massive hepatomegaly and severe physical and social handi...
Background: Liver transplantation (LT) for polycystic liver disease (PLD) has evolved to be an optio...
Patients with end-stage isolated polycystic liver disease (PCLD) suffer from incapacitating symptoms...
Item does not contain fulltextPatients with end-stage isolated polycystic liver disease (PCLD) suffe...
BACKGROUND: Polycystic liver disease (PLD) is due to a genetic disorder and frequently coexists wit...
Introduction: Massive handicapping hepatomegaly due to adult polycystic liver disease (PLD) is accep...
ObjectiveTo analyze a 28-year single-center experience with orthotopic liver transplantation (OLT) f...
AbstractBackgroundThe Model for End‐stage Liver Disease (MELD) has been used as a prognostic tool si...
Introduction: Massive handicapping hepatomegaly due to PLD is accepted as indication for LT. In the ...
AbstractBackgroundThe purpose of this study was to determine peri‐operative mortality and long‐term ...
Polycystic liver disease (PLD) is a celiopathy characterized by progressive growth of multiple hepat...
Introduction Liver transplantation is the only curative option for patients with polycystic liver...
Introduction: Polycystic liver disease (PCLD) occurs either in an isolated form (Autosomal Dominant ...
OBJECTIVE: In an attempt to refine the indications for liver resection (LR) for highly symptomatic p...
AbstractBackground: Liver transplantation (LT) for polycystic liver disease (PLD) has evolved to be ...
Polycystic liver disease (PLD) may provoke massive hepatomegaly and severe physical and social handi...
Background: Liver transplantation (LT) for polycystic liver disease (PLD) has evolved to be an optio...
Patients with end-stage isolated polycystic liver disease (PCLD) suffer from incapacitating symptoms...
Item does not contain fulltextPatients with end-stage isolated polycystic liver disease (PCLD) suffe...
BACKGROUND: Polycystic liver disease (PLD) is due to a genetic disorder and frequently coexists wit...
Introduction: Massive handicapping hepatomegaly due to adult polycystic liver disease (PLD) is accep...
ObjectiveTo analyze a 28-year single-center experience with orthotopic liver transplantation (OLT) f...
AbstractBackgroundThe Model for End‐stage Liver Disease (MELD) has been used as a prognostic tool si...
Introduction: Massive handicapping hepatomegaly due to PLD is accepted as indication for LT. In the ...