These guidelines address management of patients with autosomal dominant polycystic kidney disease who are candidates for kidney and/or liver transplantation. The guidelines include such issues as qualifying for transplantation, indications for nephrectomy, indications for simultaneous kidney and liver transplantation, qualification of a living donor, and qualification for renal replacement therapy in patients with a failing transplanted kidney
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Autosomal dominant polycystic kidney disease (ADPKD) is the reported etiology in 10% of end-stage ki...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
These guidelines address the management of patients with autosomal dominant polycystic kidney diseas...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent cause of genetic renal dis...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Autosomal dominant polycystic kidney disease (ADPKD) is the first genetic cause of end-stage renal d...
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited nephropathy. Initi...
International audienceOBJECTIVES:To perform a state of the art about autosomal dominant polykystic k...
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early onset...
Aim. To investigate the renal transplantation results for patients with end-stage renal disease (ESR...
BACKGROUND: The choice for either kidney or combined liver-kidney transplantation in young people wi...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Autosomal dominant polycystic kidney disease (ADPKD) is the reported etiology in 10% of end-stage ki...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
These guidelines address the management of patients with autosomal dominant polycystic kidney diseas...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent cause of genetic renal dis...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Autosomal dominant polycystic kidney disease (ADPKD) is the first genetic cause of end-stage renal d...
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited nephropathy. Initi...
International audienceOBJECTIVES:To perform a state of the art about autosomal dominant polykystic k...
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early onset...
Aim. To investigate the renal transplantation results for patients with end-stage renal disease (ESR...
BACKGROUND: The choice for either kidney or combined liver-kidney transplantation in young people wi...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Autosomal dominant polycystic kidney disease (ADPKD) is the reported etiology in 10% of end-stage ki...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...