ReviewClinical and translational science2011
Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease.
Review in Clinical and translational science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
15 citing papers in PubMed, 42 citations in OpenAlex.
- ZFYVE19 deficiency: a ciliopathy involving failure of cell division, with cell death.Journal of medical genetics · 2024Article
- Evaluation of galectin-3 and intestinal fatty acid binding protein as serum biomarkers in autosomal recessive polycystic kidney disease.Journal of nephrology · 2023Article
- Macroscopic hematuria in a child with portal hypertension: Answers.Pediatric nephrology (Berlin, Germany) · 2021Article
- Autosomal Recessive Polycystic Kidney Disease-The Clinical Aspects and Diagnostic Challenges.Journal of pediatric genetics · 2021Review
- Congenital Hepatic Fibrosis Presenting With Pancytopenia.JPGN reports · 2021Article
- Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease.Radiology case reports · 2019Article
- Increased YAP Activation Is Associated With Hepatic Cyst Epithelial Cell Proliferation in ARPKD/CHF.Gene expression · 2017Article
- Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease.Frontiers in pediatrics · 2017Review
- Evidence for a "Pathogenic Triumvirate" in Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney Disease.BioMed research international · 2016Review
- Magnetic resonance microscopy of renal and biliary abnormalities in excised tissues from a mouse model of autosomal recessive polycystic kidney disease.Physiological reports · 2015Article
- [Congenital hepatic fibrosis with polycystic kidney diseases: case report].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2015Article
- Caroli's disease misdiagnosed as intraductal papillary neoplasm of the bile duct.Clinical and molecular hepatology · 2015Article
- Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects.Pediatrics · 2014Review
- MALDI imaging MS reveals candidate lipid markers of polycystic kidney disease.Journal of lipid research · 2013Article
- New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications.Pediatric transplantation · 2013Review
Corrections and comments
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Authors and funding
1 author at 1 institution in 1 country.
Funding
Abstract
Autosomal recessive polycystic kidney disease (ARPKD) is a developmental disorder that mainly affects the kidneys and the biliary tract. Affected patients often have massively enlarged cystic kidneys as well as congenital hepatic fibrosis (CHF) characterized by dilated bile ducts and associated peribiliary fibrosis. This review will examine what is known about ARPKD-associated liver disease and will highlight areas of ongoing research into its pathogenesis and potential treatment.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.