Caroli disease: an update on pathogenesis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine,General Medicine
Reference10 articles.
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2. Caroli's disease: a report of 14 patients and review of the literature;Zhang;J Dig Dis,2012
3. Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD);Adeva;Medicine (Baltimore),2006
4. The cAMP effectors Epac and protein kinase a (PKA) are involved in the hepatic cystogenesis of an animal model of autosomal recessive polycystic kidney disease (ARPKD);Banales;Hepatology (Baltimore, MD),2009
5. Activation of the MEK5/ERK5 cascade is responsible for biliary dysgenesis in a rat model of Caroli's disease;Sato;Am J Pathol,2005
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1. Caroli's disease misdiagnosed as bile duct cystadenoma: A case report;Journal of Clinical Ultrasound;2024-04-02
2. Histopathology and molecular pathology confirmed a diagnosis of atypical Caroli’s syndrome: a case report;Diagnostic Pathology;2024-02-22
3. Caroli disease combined with Banti syndrome in a woman: a case report;Journal of International Medical Research;2024-01
4. Early onset Caroli’s disease with associated renal cystic disease presented with recurrent fever and epigastric pain: a case report;Egyptian Pediatric Association Gazette;2023-10-19
5. Maternal choledochal cysts in pregnancy: A systematic review of case reports and case series;World Journal of Gastrointestinal Surgery;2023-08-27
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