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American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 11/2009, Volume 151C, Issue 4, pp. 296 - 306
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 1/2016, Volume 31, Issue 1, pp. 113 - 119
Hepatorenal fibrocystic diseases (HRFCDs) are a group of monogenic disorders characterized by developmental abnormalities involving the liver and kidney. In... 
Pediatrics | Autosomal-recessive polycystic kidney disease | Ciliopathy | Nephrology | Nephronophthisis 13 | Medicine & Public Health | Congenital hepatic fibrosis | Caroli disease | Urology | Hepatorenal fibrocystic disease | GENOTYPE-PHENOTYPE CORRELATION | DIAGNOSIS | MANAGEMENT | CILIOPATHIES | POLYCYSTIC KIDNEY-DISEASE | DISORDERS | MECHANISMS | LIVER-DISEASE | CILIA | PATHOGENESIS | UROLOGY & NEPHROLOGY | PEDIATRICS | Polycystic Kidney Diseases - genetics | Predictive Value of Tests | Polycystic Kidney Diseases - diagnosis | Genetic Testing | Prognosis | Age Factors | Encephalocele - epidemiology | Humans | Genetic Diseases, Inborn - genetics | Child, Preschool | Caroli Disease - diagnosis | Infant | Male | Genetic Diseases, Inborn - epidemiology | Polycystic Kidney, Autosomal Recessive - diagnosis | Caroli Disease - genetics | Polycystic Kidney, Autosomal Recessive - genetics | Liver Cirrhosis - epidemiology | Renal Insufficiency, Chronic - epidemiology | Young Adult | Caroli Disease - epidemiology | Adult | Female | Republic of Korea - epidemiology | Child | Genetic Diseases, Inborn - diagnosis | Liver Cirrhosis - genetics | Encephalocele - genetics | Ciliary Motility Disorders - epidemiology | Encephalocele - diagnosis | Genetic Predisposition to Disease | Liver Cirrhosis - diagnosis | Risk Factors | Polycystic Kidney, Autosomal Recessive - epidemiology | Phenotype | Kidney Failure, Chronic - epidemiology | Adolescent | Ciliary Motility Disorders - diagnosis | Polycystic Kidney Diseases - epidemiology | Ciliary Motility Disorders - genetics
Journal Article
Journal of Obstetrics and Gynaecology Canada, ISSN 1701-2163, 12/2017, Volume 39, Issue 12, pp. 1176 - 1179
Caroli disease is a very rare congenital anomaly characterized by non-obstructive saccular or fusiform dilatation of the intrahepatic bile ducts. It is... 
autosomal recessive polycystic kidney disease | 3-D ultrasound | MRI | Caroli disease | Pregnancy | Magnetic Resonance Imaging | Ultrasonography, Prenatal | Humans | Caroli Disease - diagnostic imaging | Adult | Female | Imaging, Three-Dimensional | Polycystic Kidney, Autosomal Recessive - diagnostic imaging
Journal Article
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, ISSN 0254-8860, 09/2014, Volume 33, Issue 5, p. 500
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s12664-013-0403-5 
Young Adult | Cholangiography | Humans | Diffusion Magnetic Resonance Imaging | Caroli Disease - diagnosis | Male | Biomarkers - blood | Caroli Disease - pathology
Journal Article
Alimentary Pharmacology & Therapeutics, ISSN 0269-2813, 10/2008, Volume 28, Issue 8, pp. 953 - 965
Summary Background  The increasing use of imaging modalities has led to the detection of more liver masses. The differential diagnosis of a focal liver mass... 
Cystadenoma - diagnosis | Diagnosis, Differential | Liver Neoplasms - diagnosis | Adenoma, Liver Cell - diagnosis | Humans | Focal Nodular Hyperplasia - diagnosis | Magnetic Resonance Imaging - methods | Tomography, X-Ray Computed - methods | Caroli Disease - diagnosis | Cysts - diagnosis | Hemangioma - diagnosis | Liver
Journal Article
Journal Article