Results 11 to 20 of about 54,042 (201)
Polycystic Kidney Disease [PDF]
The Polycystic Kidney Disease (PKD) is a genetic disease which is characterized by the gradual emergence of cystic lesions in the kidneys, which replace the renal parenchyma causing deterioration of its function to stage 5. The PKD is one of the causes of Chronic Kidney Disease on renal replacement therapy (RRT).
Lavie, C.J. +3 more
openaire +3 more sources
Predictors and outcomes of laparoscopic nephrectomy in autosomal dominant polycystic kidney disease [PDF]
Purpose: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, and 20% of patients eventually require nephrectomies due to compressive symptoms or renal-related complications. Traditionally, nephrectomies were
Kenneth Chen +5 more
doaj +1 more source
Polycystic Kidney Disease Drug Development: A Conference Report
Autosomal dominant polycystic kidney disease (ADPKD) is part of a spectrum of inherited diseases that also includes autosomal recessive polycystic kidney disease, autosomal dominant polycystic liver disease, and an expanding group of recessively ...
Max C. Liebau +4 more
doaj +1 more source
Feline Polycystic Kidney Disease: An Update
Polycystic kidney disease (PKD) is a disease that affects felines and other mammals, such as humans. The common name is autosomal dominant polycystic kidney disease (ADPKD) and causes a progressive development of fluid-filled cysts in the kidney and ...
Lorie Schirrer +2 more
doaj +1 more source
Radiological Imaging Diagnosis of Adult Renal Cystic Diseases and Management
Background: Renal cysts are a heterogonous group of cystic renal diseases that present in approximately 40% of the patients undergoing imaging. Objective: To describe the role of the radiological imaging methods for the diagnosis of adult renal ...
Saleh Akares, Ahmed Bahomil
doaj +1 more source
Phase Separation in Kidney Diseases: Autosomal Dominant Polycystic Kidney Disease and Beyond
Background: The formation of biomolecular condensates via phase separation has emerged as a fundamental principle underlying the spatiotemporal coordination of biological activities in cells.
Lirong Zhang +4 more
doaj +1 more source
Femoral Neuropathy Secondary to Autosomal Dominant Polycystic Kidney Disease: A Case Report [PDF]
Compressive femoral neuropathy is a disabling condition accompanied by difficulty in hip flexion and knee extension. It may result from retroperitoneal hematoma or bleeding, or from complications associated with pelvic, hip surgery, and renal transplants.
Jeehyun Yoo +5 more
doaj +1 more source
Beyond polycystic kidney disease [PDF]
Tuberous sclerosis(TS) is an autosomal dominant disease caused by mutations inTSC1andTSC2genes.TSC2gene is located in chromosome 16p13.3, adjacent toPKD1gene, responsible for the autosomal dominant polycystic kidney disease. In a rare subgroup of patients, the presence of a deletion which simultaneously affects theTSC2andPKD1genes has been confirmed ...
Santos, SF +3 more
openaire +3 more sources
Gene therapy for pediatric genetic kidney diseases
Genetic kidney disease is the main cause of chronic kidney disease in children. While the pathogenic genes associated with most genetic kidney diseases have been identified, the underlying mechanisms of disease initiation remain ambiguous, and effective ...
Yi Lu +4 more
doaj +1 more source
Fetal polycystic kidney disease: Pathological overview
Polycystic kidney disease is a rare developmental anomaly inherited as autosomal dominant or autosomal recessive. It is characterized by cystic dilatation of the collecting ducts frequently associated with hepatic involvement and progression to renal ...
Sunita B Patil +3 more
doaj +1 more source

