Disease: Polycystic kidney disease- type 2
- A case of late-onset organizing pneumonia following COVID-19 infection in a post-kidney transplant patient
- A de novo PKD1 mutation in a Chinese family with autosomal dominant polycystic kidney disease
- Additional renoprotective effect of the SGLT2 inhibitor dapagliflozin in a patient with ADPKD receiving tolvaptan treatment
- An Artificial Intelligence Generated Automated Algorithm to Measure Total Kidney Volume in ADPKD
- Approach to simple kidney cysts in children
- Asymmetric synthesis of P-stereogenic phosphindane oxides via kinetic resolution and their biological activity
- Atypical Manifestation of Adult Polycystic Kidney Disease in an Elderly Individual
- Autosomal dominant polycystic kidney disease and pericardial effusion: coincidence? I think not! Case report and review of the literature
- Autosomal Dominant Polycystic Kidney Disease: Extrarenal Involvement
- Benzothiazole derivatives as histone deacetylase inhibitors for the treatment of autosomal dominant polycystic kidney disease
- Can Additional Water a Day Keep the Cysts Away, in Patients with Polycystic Kidney Disease?
- Caroli's Disease Associated with Autosomal Dominant Polycystic Kidney Disease with Acute Pancreatitis: A Case Report
- Case Report: Autosomal dominant polycystic kidney disease and Wilms' tumor in infancy and childhood
- Case report: Rare genetic liver disease - a case of congenital hepatic fibrosis in adults with autosomal dominant polycystic kidney disease
- CD74 Promotes Cyst Growth and Renal Fibrosis in Autosomal Dominant Polycystic Kidney Disease
- CFAP47 is a novel causative gene implicated in X-linked polycystic kidney disease
- Characteristics and clinical outcomes of patients with kidney failure of unknown aetiology from ANZDATA registry
- Clinical Characteristics and Kidney Outcomes in Chinese Patients with Autosomal Dominant Polycystic Kidney Disease
- Clinical manifestation, epidemiology, genetic basis, potential molecular targets, and current treatment of polycystic liver disease
- Clinical Significance of the Cystic Phenotype in Alport Syndrome
- Compassionate use of tolvaptan in acquired megacolon secondary to autosomal dominant polycystic kidney disease (ADPKD)
- Comprehensive Analysis of PKD1 and PKD2 by Long-Read Sequencing in Autosomal Dominant Polycystic Kidney Disease
- Deciphering interleukin 37's therapeutic potential: insights into alleviating inflammation in autosomal dominant polycystic kidney disease
- Dual-task kidney MR segmentation with transformers in autosomal-dominant polycystic kidney disease
- Editorial: Cystic kidney diseases in children and adults: from diagnosis to etiology and back
- Elevated hemoglobin levels in renal transplant recipients with polycystic kidney disease versus other etiologies: exploring mechanisms and implications for outcomes
- End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy
- Evaluation of the Renal and Cardiovascular Effects of Long-Term Tolvaptan Treatment in Autosomal Dominant Polycystic Kidney Disease
- Evolving Diagnostic Interpretation: How Automated Algorithms for Autosomal Dominant Polycystic Kidney Disease (ADPKD) Address Inter-Reader Variability and Physician Burnout
- Exploring Adiponectin in Autosomal Dominant Kidney Disease: Insight and Implications
- Familial Variability of Disease Severity in Adult Patients With ADPKD
- Feasibility of Water Therapy for Slowing Autosomal Dominant Polycystic Kidney Disease Progression
- Genetic Analysis of Severe Polycystic Liver Disease in Japan
- Genetics of cystogenesis in base-edited human organoids reveal therapeutic strategies for polycystic kidney disease
- Genomics in the kidney clinic
- Genotype-phenotype of autosomal dominant polycystic kidney disease in Malta
- Glis2 is an early effector of polycystin signaling and a target for therapy in polycystic kidney disease
- Global analysis of urinary extracellular vesicle small RNAs in autosomal dominant polycystic kidney disease
- Grainyhead-like 2 Deficiency and Kidney Cyst Growth in a Mouse Model
- Human <em>PKD1</em> sequences form R-loop structures <em>in vitro</em>
- HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial
- Inhibiting centrosome clustering reduces cystogenesis and improves kidney function in autosomal dominant polycystic kidney disease
- Inhibition of pannexin-1 does not restore electrolyte balance in precystic Pkd1 knockout mice
- Initial eGFR Changes Predict Response to Tolvaptan in ADPKD
- Interleukin-37: a new therapeutic target in autosomal dominant polycystic kidney disease
- Investigation of Basolateral Targeting Micelles for Drug Delivery Applications in Polycystic Kidney Disease
- Investigational agents for autosomal dominant polycystic kidney disease: preclinical and early phase study insights
- Kidney Cysts in Children With Alport Syndrome: A Report of 3 Cases
- Kidney Disease and Proteomics: A Recent Overview of a Useful Tool for Improving Early Diagnosis
- Kidney Energetics and Cyst Burden in Autosomal Dominant Polycystic Kidney Disease: A Pilot Study
- Kidney Stones Account for Increased Imaging Studies in Autosomal Dominant Polycystic Kidney Disease
- Laparoscopic Nephrectomy Via the Retroperitoneal Approach for Autosomal Dominant Polycystic Kidney Disease After Renal Transplant: A Case Report
- Large Kidney Cysts in <em>HNF1B</em> Nephropathy Mimicking Autosomal Dominant Polycystic Kidney Disease
- Large Kidney Cysts in HNF1B Nephropathy Mimicking Autosomal Dominant Polycystic Kidney Disease
- Leucine-Rich Repeat in Polycystin-1 Suppresses Cystogenesis in a Zebrafish (Danio rerio) Model of Autosomal-Dominant Polycystic Kidney Disease
- Long-Residence Time Peptide Antagonist for the Vasopressin V(2) Receptor to Treat Autosomal Dominant Polycystic Kidney Disease
- Long-term effectiveness and safety of tolvaptan in autosomal dominant polycystic kidney disease
- Long-Term Effects of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease: Predictors of Treatment Response and Safety over 6 Years of Continuous Therapy
- Long-term expandable mouse and human-induced nephron progenitor cells enable kidney organoid maturation and modeling of plasticity and disease
- Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease
- Mechanistic complement of autosomal dominant polycystic kidney disease: the role of aquaporins
- Molecular and structural basis of the dual regulation of the polycystin-2 ion channel by small-molecule ligands
- Monoallelic pathogenic IFT140 variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotype
- Mortality risk in patients with autosomal dominant polycystic kidney disease
- Multidisciplinary management improves the genetic diagnosis of hereditary kidney diseases in the next generation sequencing (NGS) era
- Native nephrectomy in polycystic kidney disease patients on transplant lists: how and when?
- Nephronophthisis-associated FBW7 mediates cyst-dependent decline of renal function in ADPKD
- nnUNet for Automatic Kidney and Cyst Segmentation in Autosomal Dominant Polycystic Kidney Disease
- Notch3 as a novel therapeutic target for the treatment of ADPKD by regulating cell proliferation and renal cyst development
- Novel Potential Therapeutic Targets in Autosomal Dominant Polycystic Kidney Disease from the Perspective of Cell Polarity and Fibrosis
- Overexpression of SMYD3 Promotes Autosomal Dominant Polycystic Kidney Disease by Mediating Cell Proliferation and Genome Instability
- Pain and Health-Related Quality of Life in Autosomal Dominant Polycystic Kidney Disease: Results from a National Patient-Powered Registry
- Polycystin-2 Mediated Calcium Signalling in the Dictyostelium Model for Autosomal Dominant Polycystic Kidney Disease
- Quantitative susceptibility mapping for detection of kidney stones, hemorrhage differentiation, and cyst classification in ADPKD
- Renal Hemodynamic and Functional Changes in ADPKD Patients
- Renal Pathology of Ciliopathies
- Role of Female Sex Hormones in ADPKD Progression and a Personalized Approach to Contraception and Hormonal Therapy
- Safety and efficacy of transcatheter arterial embolization in autosomal dominant polycystic kidney patients with gross hematuria: Six case reports
- Safety of Docetaxel in a Patient with Metastatic Castration-Resistant Prostate Cancer After Kidney Transplantation: A Case Report
- Secondary infertility due to necrospermia in men with autosomal-dominant polycystic kidney disease: a report of two cases
- Single-Center Experience of Pediatric Cystic Kidney Disease and Literature Review
- Structural basis for CFTR inhibition by CFTR<sub>inh</sub>-172
- Symptomatic polycystic liver disease: a rare indication of hepatectomy
- The effect of primary renal disease upon outcomes after renal transplant
- The Han:SPRD Rat: A Preclinical Model of Polycystic Kidney Disease
- The Importance of Recognizing Pain in Patients With Autosomal Dominant Polycystic Kidney Disease
- The Link between Autosomal Dominant Polycystic Kidney Disease and Chromosomal Instability: Exploring the Relationship
- The pathophysiology of polycystic liver disease
- The Role of the L-Arginine-Nitric Oxide Molecular Pathway in Autosomal Dominant Polycystic Kidney Disease
- The screening, diagnosis, and management of patients with autosomal dominant polycystic kidney disease: A national consensus statement from Taiwan
- Tolvaptan and Number Needed to Harm in Autosomal Dominant Polycystic Kidney Disease
- Tolvaptan Treatment and Long-Term Impact on Quality of Life in Autosomal Dominant Polycystic Kidney Disease Patients: A Pilot Study
- Treatment for patients with autosomal dominant polycystic kidney disease in the chronic kidney disease without kidney replacement therapy in real-world clinical practice: a descriptive retrospective cohort study
- Ultra high frequency ultrasound enables real-time visualization of blood supply from chorioallantoic membrane to human autosomal dominant polycystic kidney tissue
- Ultrasound features of a bilineal inheritance of autosomal dominant polycystic kidney disease
- US Veterans Administration Autosomal Dominant Polycystic Kidney Disease Cohort: Demographic, Comorbidity and Key Laboratory Data Characteristics
- Validation of the Mayo Imaging Classification System for Predicting Kidney Outcomes in ADPKD
- Vascular Access Outcomes in Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- Visceral Adiposity and Progression of ADPKD: A Cohort Study of Patients From the TEMPO 3:4 Trial
- YouTube(TM) as a source of information on autosomal dominant polycystic kidney disease: A quality analysis