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Netherlands Journal of Medicine, ISSN 0300-2977, 07/2018, Volume 76, Issue 5, pp. 226 - 234
Background: Cyst infection may occur in autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver disease (ADPLD).... 
ADPLD | Cyst infection | ADPKD | REGRESSION | MEDICINE, GENERAL & INTERNAL | IMPUTATION | IMPACT | IMMUNOSUPPRESSION | cyst infection | DIAGNOSTIC-CRITERIA | COMPUTED-TOMOGRAPHY | TRANSPLANTATION
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2018, Volume 102, Issue 5, pp. 832 - 844
Journal Article
Liver International, ISSN 1478-3223, 03/2019, Volume 39, Issue 3, pp. 575 - 582
Background & Aims Polycystic liver disease (PLD) occurs in two genetic disorders, autosomal-dominant polycystic kidney disease (ADPKD) and autosomal-dominant... 
ADPLD | ADPKD | risk factors | polycystic liver disease | KIDNEY-DISEASE | EFFICACY | VOLUME | VALIDATION | SYMPTOMS | WOMEN | POOLED ANALYSIS | WEIGHT | GASTROENTEROLOGY & HEPATOLOGY | LANREOTIDE | PROGRESSION | Diagnostic imaging | Liver diseases | Kidney diseases | Risk factors | Beer | Phenotypes | Polycystic kidney | Liver | Regression analysis | Males | Risk analysis | Patients | Subgroups | Magnetic resonance imaging | Computed tomography | Cysts | Diagnosis | Females | Age
Journal Article
Clinical and Experimental Nephrology, ISSN 1342-1751, 6/2019, Volume 23, Issue 6, pp. 825 - 833
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2012, Volume 56, Issue 5, pp. 1201 - 1203
Autosomal dominant polycystic liver disease results from mutations in PRKCSH or SEC63. The respective gene products, glucosidase IIβ and SEC63p, function in... 
PRKCSH | Dosage theory | PKD1/PKD2 | Fibrocystin/polyductin | Polycystic liver disease (ADPLD) | PKHD1 | Polycystic kidney disease (ADPKD, ARPKD) | Variable disease expression | Dosage-sensitive network | Polycystin-1/-2 | Modifier | Cilia | SEC63 | OVEREXPRESSION | CYST FORMATION | AUTOSOMAL-DOMINANT | MUTATIONS | GASTROENTEROLOGY & HEPATOLOGY
Journal Article
United European Gastroenterology Journal, ISSN 2050-6406, 2/2018, Volume 6, Issue 1, pp. 81 - 88
Background Symptoms in polycystic liver disease (PLD) are thought to be caused by compression of organs and structures by the enlarged liver. Aim The aim of... 
symptoms | hepatomegaly | quality of life | autosomal dominant polycystic liver disease (ADPLD) | Autosomal dominant polycystic kidney disease (ADPKD) | KIDNEY-DISEASE | VALIDATION | GASTROENTEROLOGY & HEPATOLOGY | Original
Journal Article
Journal Article
World Journal of Gastroenterology, ISSN 1007-9327, 2005, Volume 11, Issue 48, pp. 7690 - 7693
Journal Article
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, ISSN 2542-4548, 06/2019, Volume 3, Issue 2, pp. 149 - 159
To describe first episodes of bacterial cholangitis complicating autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver... 
Journal Article
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