Abstract The 2020 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice
Guideline on the Evaluation and Management of Candidates for Kidney Transplantation is …

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary
kidney disease and one of the most common causes of end-stage kidney disease. Multiple …

Abstract The 2017 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice
Guideline on the Evaluation and Care of Living Kidney Donors is intended to assist medical …

Genetic diseases cause numerous complex and intractable pathologies. DNA sequences
encoding each human's complexity and many disease risks are contained in the …

Autosomal dominant polycystic kidney disease (ADPKD) is an inherited multisystem
disorder, characterized by renal and extra-renal fluid-filled cyst formation and increased …

Autosomal dominant polycystic kidney disease (ADPKD), the most frequent cause of genetic
renal disease affecting approximately 4 to 7 million individuals worldwide and accounting for …

ADPKD patients benefit from specialized care over their lifetimes, starting with diagnosis of
the condition with ongoing discussion of both the renal course and extra-renal issues. Both …

Objectives New-onset diabetes after kidney transplantation (NODAT) is associated with both
renal allograft failure and increased rates of mortality. The objective of this meta-analysis …

Polycystic kidney disease is cilia-related kidney disorder and a common cause of endstage
kidney disease (ESKD) both in children and adults. Autosomal dominant polycystic kidney …

Introduction To evaluate the feasibility of simultaneous unilateral nephrectomy with kidney
transplantation and to determine the effect of this procedure on perioperative morbidity and …