Add to ORKGThe experience of combined liver-kidney transplantation (CLKT) is limited in pediatric populations. This strategy is, however, required in specific diseases such as metabolic diseases (namely primary hyperoxaluria type one and methylmalonic acidemia), autosomal recessive polycystic kidney disease, miscellaneous ciliopathies and atypical hemolytic uremic syndrome.status: publishe
BACKGROUND/AIM: The main indications for combined liver and kidney transplantation (CLKT) are as fo...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...
Background. Renal insufficiency is increasingly common in end-stage liver disease and allocation of ...
Background Experience in combined liver-kidney transplantation (CLKT) in children is limited. Method...
Combined liver-kidney transplantation (CLKT) in children is uncommon and outcomes have not been well...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
Introduction. Primary hyperoxaluria type-1 (PHI) is an autosomal recessive disorder caused by impair...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
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...
OBJECTIVES: MMA is associated with chronic tubulointerstitial nephritis and a progressive decline in...
The main indications for combined liver and kidney transplantation (CLKT) are as follows: (1) cirrho...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
BACKGROUND/AIM: The main indications for combined liver and kidney transplantation (CLKT) are as fo...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...
Background. Renal insufficiency is increasingly common in end-stage liver disease and allocation of ...
Background Experience in combined liver-kidney transplantation (CLKT) in children is limited. Method...
Combined liver-kidney transplantation (CLKT) in children is uncommon and outcomes have not been well...
The choice for either kidney or combined liver-kidney transplantation in young people with kidney fa...
Introduction. Primary hyperoxaluria type-1 (PHI) is an autosomal recessive disorder caused by impair...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
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...
OBJECTIVES: MMA is associated with chronic tubulointerstitial nephritis and a progressive decline in...
The main indications for combined liver and kidney transplantation (CLKT) are as follows: (1) cirrho...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
Objective Adult Polycystic liver disease (PLD) is frequently associated with autosomal dominant poly...
BACKGROUND/AIM: The main indications for combined liver and kidney transplantation (CLKT) are as fo...
Several metabolic monogenic diseases may be cured by liver transplantation alone (LTA) or by combine...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...