Results 61 to 70 of about 8,116 (160)
Clinical Case Reports, Volume 13, Issue 6, June 2025.ABSTRACT Polycystic liver disease is a hereditary disease, which is characterized by the presence of multiple cysts within the liver. In this case, we report a patient with multiple cysts in the kidneys and liver, who underwent kidney transplantation in 2019 and then liver transplantation 4 years later.
Chengjun Sun +4 more
wiley +1 more source
Management of Pain in Autosomal Dominant Polycystic Kidney Disease and Anatomy of Renal Innervation [PDF]
, 2015 Purpose Chronic pain is a prominent feature of autosomal dominant polycystic kidney disease that is difficult to treat and manage, often resulting in a decrease in quality of life.
Bacallao, Robert L. +4 more
core +1 more source
Determinants of Renal Disease Variability in ADPKD [PDF]
Advances in Chronic Kidney Disease, 2010 In common with other Mendelian diseases, the presentation and progression of autosomal dominant polycystic kidney disease (ADPKD) vary widely in the population. The typical course is of adult-onset disease with ESRD in the 6th decade. However, a small proportion has adequate renal function into the 9th decade, whereas others present with enlarged ...
Sandro Rossetti, Peter C. Harris
openaire +3 more sources
A Rare Diagnosis of Caroli Syndrome in a Young Patient
Clinical Case Reports, Volume 13, Issue 6, June 2025.ABSTRACT Caroli syndrome is a rare but serious congenital disorder associated with portal hypertension and polycystic kidney disease. Early diagnosis via imaging, particularly MRCP, is crucial to prevent life‐threatening complications such as cholangitis and biliary cirrhosis.
Elaheh Karimzadeh‐Soureshjani +4 more
wiley +1 more source
From the Cover: Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel [PDF]
, 2000 Silvia González‐Perrett
openalex +2 more sources
Chronic subdural haematoma and arachnoid cyst in autosomal dominant polycystic kidney disease (ADPKD) [PDF]
, 2005 We present the unusual association between chronic subdural haematoma (CSDH), intracranial arachnoid cyst and autosomal dominant polycystic kidney disease (ADPKD) in a 27-year-old man. CSDH is a documented complication of intracranial arachnoid cyst, the
Leung, GKK, Yiu, WF
core +1 more source
Computational Drug Repositioning in Cardiorenal Disease: Opportunities, Challenges, and Approaches
PROTEOMICS, EarlyView.
Paul Perco +7 more
wiley +1 more source
Contemporary Perspectives on Chronic Renal Disorders
Chronic Diseases and Translational Medicine, Volume 11, Issue 2, Page 89-104, June 2025.ABSTRACT The prevalence of renal diseases and its associated burden on healthcare have tremendously risen in the past few years. From simple markers assessing kidney function, current renal research delves into understanding the diseases at the cellular and molecular levels and not just at treating, but at improving quality of life, arresting ...
Deenadhayalan Ashok +5 more
wiley +1 more source
Urine Fetuin-A is a biomarker of autosomal dominant polycystic kidney disease progression. [PDF]
, 2015 BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by numerous fluid-filled cysts that frequently result in end-stage renal disease. While promising treatment options are in advanced clinical development,
Bernet, F. +11 more
core +2 more sources
Psychiatry and Clinical Neurosciences Reports, Volume 4, Issue 2, June 2025.Table 3 shows the results of the multiple logistic regression analysis. The relationship between Stanford Integrated Psychosocial Assessment for Transplantation (SIPAT) and medication nonadherence (MNA) was examined, controlling for age, sex, and employment status.
Kosuke Takano +7 more
wiley +1 more source