Add to ORKGThe choice for either kidney or combined liver-kidney transplantation in young people with kidney failure and liver fibrosis due to autosomal recessive polycystic kidney disease (ARPKD) can be challenging. We aimed to analyze the characteristics and outcomes of transplantation type in these children, adolescents, and young adults.status: publishe
Background: Thailand has a population of 65 million. The estimated incidence of chronic kidney disea...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
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...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
BACKGROUND: The choice for either kidney or combined liver-kidney transplantation in young people wi...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
International audienceBackground and objectives. In contrast to the improvement in our understanding...
Autosomal recessive polycystic kidney disease (ARPKD) is a rare but frequently severe disorder that ...
Autosomal recessive polycystic kidney disease (ARPKD) is a severe pediatric hepatorenal disorder wit...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
The experience of combined liver-kidney transplantation (CLKT) is limited in pediatric populations. ...
Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phen...
BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) shows a great phenotypic variabili...
Background: Thailand has a population of 65 million. The estimated incidence of chronic kidney disea...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
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...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
BACKGROUND: The choice for either kidney or combined liver-kidney transplantation in young people wi...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
International audienceBackground and objectives. In contrast to the improvement in our understanding...
Autosomal recessive polycystic kidney disease (ARPKD) is a rare but frequently severe disorder that ...
Autosomal recessive polycystic kidney disease (ARPKD) is a severe pediatric hepatorenal disorder wit...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple m...
The experience of combined liver-kidney transplantation (CLKT) is limited in pediatric populations. ...
Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phen...
BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) shows a great phenotypic variabili...
Background: Thailand has a population of 65 million. The estimated incidence of chronic kidney disea...
In patients with autosomal dominant polycystic kidney disease (ADPKD) evaluated for kidney transplan...
Polycystic disease causes a progressive decrease in renal function and liver degeneration. The progr...