Polycystic liver diseases (PLDs) are inherited genetic disorders characterized by
progressive development of intrahepatic, fluid-filled biliary cysts (more than ten), which …

Polycystic liver disease (PLD) is a rare hereditary disease that independently exists in
isolated PLD, or as an accompanying symptom of autosomal dominant polycystic kidney …

Polycystic liver disease (PLD) is a clinical condition characterized by the presence of more
than 10 cysts in the liver. It is a rare disease Of genetic etiology that presents as an isolated …

Objectives: Although a number of genetic forms of cholestasis have been identified, the
genetic etiology of disease remains unidentified in a subset of cholestasis patients. Methods …

Liver transplantation (LT) is currently considered the gold standard treatment for end-stage
liver failure. Compared to the first decades of its use, LT is associated with lower comorbidity …

Benign liver lesions are increasingly diagnosed in daily clinical practice due to the growing
use of imaging techniques for the study of the abdomen in patients who have non-specific …

Originating from ectodermal epithelium, radial glial cells (RGCs) retain apico-basolateral
polarity and comprise a pseudostratified epithelial layer in the developing cerebral cortex …

Cystic lesions of the liver may be classified as parasitic and nonparasitic. The main parasitic
cystic lesion of the liver is hydatid disease. Nonparasitic lesions are again divided into …

Background & aims Loss of primary cilia in epithelial cells is known to cause cystic diseases
of the liver and kidney. We have previously shown that during experimental and human …

OBJECTIVE To characterize the association between peritoneopericardial diaphragmatic
hernia (PPDH) or congenital central diaphragmatic hernia (CCDH) and ductal plate …