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Treatment persistence to tolvaptan in patients with autosomal dominant polycystic kidney disease: a secondary use of data analysis of patients in the IMADJIN® dataset

Safety and efficacy of Tolvaptan in real-world patients with autosomal dominant polycystic kidney disease- interim results of SLOW-PKD surveillance

Genes, Vol. 12, Pages 1401: Whole Exome Sequencing in a Series of Patients with a Clinical Diagnosis of Tuberous Sclerosis Not Confirmed by Targeted TSC1/TSC2 Sequencing

Polycystic liver and kidney diseases.

Polycystic liver and kidney diseases.

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-

Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-

A Human Multi-Lineage Hepatic Organoid Model for Liver Fibrosis

Biomedicines, Vol. 10, Pages 290: Quantitative Proteomic Study Unmasks Fibrinogen Pathway in Polycystic Liver Disease

IJMS, Vol. 22, Pages 6523: Molecular Pathophysiology of Autosomal Recessive Polycystic Kidney Disease

Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells Running title: Cystin deficiency reduces FPC levels through enhanced autophagic degradation.

IJMS, Vol. 21, Pages 6093: Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic Treatment

Genetic and Sporadic Renal Cystic Diseases During the Perinatal and Neonatal Period: Core Curriculum 2021.

Liver Disease in Autosomal Recessive Polycystic Kidney Disease - Clinical Characteristics and Management in Relation to Renal Failure.

Prevalence, risk factors and disease knowledge of polycystic kidney disease in Pakistan.

Mutations in PMM2 gene in four unrelated Spanish families with polycystic kidney disease and hyperinsulinemic hypoglycemia.

Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 alleles

Detection of <em>PKD1</em> and <em>PKD2</em> Somatic Variants in Autosomal Dominant Polycystic Kidney Cyst Epithelial Cells by Whole-Genome Sequencing

Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes

Long-term pulmonary function in children with recessive polycystic kidney disease.

Long-term pulmonary function in children with recessive polycystic kidney disease.

Long-term pulmonary function in children with recessive polycystic kidney disease

Long-term pulmonary function in children with recessive polycystic kidney disease

Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis.

Genes, Vol. 12, Pages 1762: Nephronophthisis-Pathobiology and Molecular Pathogenesis of a Rare Kidney Genetic Disease

Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic Treatment.

Preimplantation Genetic Testing for Monogenic Kidney Disease

Type IV choledochal cyst with polycystic kidney disease: a case report

Combined liver and kidney transplantation in children.

Molecular genetics of renal ciliopathies

The genetics of Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Brucella Peritonitis in a Patient on Peritoneal Dialysis: A Case Report and Review of Literature

Identification of Two Novel Mutations in <em>PKHD1</em> Gene from Two Families with Polycystic Kidney Disease by Whole Exome Sequencing

Autosomal-rezessive polyzystische Nierenerkrankung (ARPKD)

Long-Term Outcomes and Health Perceptions in Pediatric-Onset Portal Hypertension Complicated by Varices.

Long-term Outcomes and Health Perceptions in Pediatric-onset Portal Hypertension Complicated by Varices

Multiple cerebral aneurysms in an adult patient with autosomal recessive polycystic kidney disease

Autosomal recessive polycystic kidney disease

Nonsense-associated alternative splicing as a putative reno-protective mechanism in Pkhd1cyli/Pkhd1cyli mutant mice

VP32.07: Prenatal diagnosis of Caroli's syndrome in association with autosomal recessive polycystic kidney disease

Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres.

The carboxy‐terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC‐activation

Giant Bilateral Adrenal Myelolipoma: Case Report

Genes, Vol. 13, Pages 394: Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes

Genes, Vol. 13, Pages 394: Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes

Caroli's Syndrome: An Early Presentation.

#18: Brincidofovir for the Treatment of Disseminated Human Adenovirus Infection in Pediatric Solid-organ Transplant Recipients