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Polycystic kidney disease

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Search Period All yearsLast 12 monthsLast 5 years Topic All topicsGeneralNutrition and dietAlternative treatment methods Type of research Any type of researchHighest level of evidence only (48)Meta-analysis (12)Treatment guideline (1)Randomized trial (17)Phase 3 study (10)Systematic review (8)Clinical trial (242)Review article (250)Early study (phase 1 or 2) (14)Case report (185)Laboratory or animal research (38)Commentary or editorial (45)Retracted publication (1) Studies currently recruiting participants only (33)

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Publications and studies (1435)

• All Patients with ADPKD Should Undergo Screening for Intracranial Aneurysms: PRO. (2024/04/01) ♡
• All Patients with ADPKD Should Undergo Screening for Intracranial Aneurysms: CON. (2024/04/01) ♡
• Serum bile acids associate with liver volume in polycystic liver disease and decrease upon treatment with lanreotide. (2024/04/01) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Modulating inflammation with interleukin 37 treatment ameliorates murine Autosomal Dominant Polycystic Kidney Disease. (2024/04/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Autosomal dominant polycystic kidney disease (ADPKD) with multiple complications: Management challenges. (2024/04/01) ♡
• Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. Effects of salt and protein intake on polyuria in V2RA-treated ADPKD patients. (2024/03/27) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Tubular changes in autosomal dominant polycystic kidney disease patients: observational study. (2024/03/01) ♡
• Repurposing calcium-sensing receptor activator drug cinacalcet for ADPKD treatment. (2024/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Splicing variant of WDR37 in a case of Neurooculocardiogenitourinary syndrome. (2024/03/01) ♡
• Matrix Metalloproteinase-7 in Urinary Extracellular Vesicles Identifies Rapid Disease Progression in Autosomal Dominant Polycystic Kidney Disease. (2024/03/01) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. A combination of β-hydroxybutyrate and citrate ameliorates disease progression in a rat model of polycystic kidney disease. (2024/03/01) ♡
• Potassium levels in women with polycystic ovary syndrome using spironolactone for long-term. (2024/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Novel homozygous mutations in TXNDC15 causing Meckel syndrome. (2024/03/01) ♡
• Joubert syndrome causing mutation in C2 domain of CC2D2A affects structural integrity of cilia and cellular signaling molecules. (2024/03/01) ♡
• Survival of Infants With Severe Congenital Kidney Disease After ECMO and Kidney Support Therapy. (2024/03/01) ♡
• PKD1 gene mutation and ultrasonographic characterization in cats with renal cysts. (2024/02/23) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Inspiring Tactics with the Improvement of Mitophagy and Redox Balance for the Development of Innovative Treatment against Polycystic Kidney Disease. (2024/02/09) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. How Does ADPKD Severity Differ Between Family Members? (2024/02/05) ♡
• Meta-analysisiAll studies on one question combined and calculated together. This is the strongest form of research that exists: a single loose study can be coincidence, dozens together much less so. The label says something about the design, not about the outcome — which can also be that something does NOT work. When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta-analysis. (2024/02/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Combined liver-kidney transplantation in pediatric patients. (2024/02/01) ♡
• Transcriptomic profiling of Polycystic Kidney Disease identifies paracrine factors in the early cyst microenvironment. (2024/02/01) ♡
• Deep learning-based automated kidney and cyst segmentation of autosomal dominant polycystic kidney disease using single vs. multi-institutional data. (2024/02/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Statin therapy in patients with early-stage autosomal dominant polycystic kidney disease: Design and baseline characteristics. (2024/02/01) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Clinical-grade human skin-derived ABCB5+ mesenchymal stromal cells exert anti-apoptotic and anti-inflammatory effects in vitro and modulate mRNA expression in a cisplatin-induced kidney injury murine model. (2024/01/11) ♡
• Mapping the landscape of research on insulin resistance: a visualization analysis of randomized clinical trials. (2024/01/09) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Role of MCP-1 as an inflammatory biomarker in nephropathy. (2024/01/04) ♡
• Ablation of Long Noncoding RNA Hoxb3os Exacerbates Cystogenesis in Mouse Polycystic Kidney Disease. (2024/01/01) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Basigin Deficiency Induces Spontaneous Polycystic Kidney in Mice. (2024/01/01) ♡
• The VUS Challenge in Cystic Kidney Disease: A Case-Based Review. (2024/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations. (2024/01/01) ♡
• First preimplantation genetic testing case of Meckel syndrome with a novel homozygous TXNDC15 variant in a non-consanguineous Chinese family. (2024/01/01) ♡
• Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Cardiovascular Involvement in Patients with Autosomal Dominant Polycystic Kidney Disease: A Review. (2024/01/01) ♡
• Familial cerebral cavernous malformation presenting with cerebellopontine angle syndrome in a patient with autosomal dominant polycystic kidney disease. (2024/01/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study. (2024/01/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Specific Nutritional Strategy Is Needed for Good Nutritional Status in Autosomal Dominant Polycystic Kidney Disease. (2024/01/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Individualized Nutritional Prescription Is Necessary for Patients With Autosomal Dominant Polycystic Kidney Disease. (2024/01/01) ♡
• Correction to: Public support for patients with intractable diseases in Japan: impact on clinical indicators from nationwide registries in patients with autosomal dominant polycystic kidney disease. (2024/01/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Amnioinfusion for Fetal Renal Failure (2024-12-20) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Genetic Testing in Autosomal Dominant Polycystic Kidney Disease (2024-12-16) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Artificial Intelligence-based Image Processing Methods to Advance the Characterization of Polycystic Kidney Disease (2024-11-14) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Shared Decision Making for Choosing Autosomal Dominant Polycystic Kidney Disease Treatment (2024-11-07) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. KidneYou - Innovative Digital Therapy (2024-11-06) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Study to Evaluate the Drug-drug Interaction of JMKX003142 in Healthy Subjects (2024-10-26) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Congenital Hepatic Fibrosis and Autosomal Recessive Polycystic Kidney Disease in Children at Sohag University Hospital (2024-09-19) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Development and Assessment of The Polycystic Liver Disease Questionnaire (PLD-Q). (2024-09-19) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. A Study to Evaluate the Effects of GLPG2737 in Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD) (2024-08-22) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Study and Management of Cystic Complications in Autosomal Dominant Polycystic Kidney Disease (2024-08-09) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Genetics in the Progression of Nephropathies (2024-05-16) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Assessment of Longitudinal Changes in Endothelial Function and Oxidative Stress in Normotensive Patients With ADPKD (2024-05-06) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions (2024-04-18) ♡

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