Pathophysiology, epidemiology, classification and treatment options for polycystic liver diseases
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Polycystic liver diseases: advanced insights into the molecular mechanismsCombined liver and kidney transplant in a patient with budd-Chiari syndrome secondary to autosomal dominant polycystic kidney disease associated with polycystic liver disease: report of a case with a 9-year follow-up.Functional Budd-Chiari Syndrome Associated With Severe Polycystic Liver Disease.Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.Fenestration of liver cysts in polycystic liver disease to improve quality of life: a case report and literature reviewAutomatic total kidney volume measurement on follow-up magnetic resonance images to facilitate monitoring of autosomal dominant polycystic kidney disease progression.Spontaneous rupture of non-parasitic or non-neoplastic multiple and giant liver cysts: report of a case.Laparoscopic surgery and polycystic liver disease: Clinicopathological features and new trends in management.Therapeutic Targets in Polycystic Liver Disease.Transarterial Embolization for Treatment of Symptomatic Polycystic Liver Disease: More than 2-year Follow-up.An update on the pathophysiology and management of polycystic liver disease.Center is an important indicator for choice of invasive therapy in polycystic liver disease.Diagnosis and treatment of benign liver nodules: Brazilian Society of Hepatology (SBH) recommendations.Survival after arterial embolization therapy in patients with polycystic kidney and liver disease.Effect of tolvaptan in a patient with autosomal dominant polycystic kidney disease after living donor liver transplantation.Liver Transplant for Unusually Large Polycystic Liver Disease: Challenges and Pitfalls.Prediction of hepatic cyst recurrence after minocycline hydrochloride aspiration sclerotherapy using cyst computed tomography values.Infectious Hepatic Cyst: An Underestimated Complication.Differentiating Cystic Liver Lesions: A Review of Imaging Modalities, Diagnosis and Management.Bile Acids as Potential Biomarkers to Assess Liver Impairment in Polycystic Kidney Disease
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P2860
Pathophysiology, epidemiology, classification and treatment options for polycystic liver diseases
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on September 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Pathophysiology, epidemiology, ...... for polycystic liver diseases
@en
Pathophysiology, epidemiology, ...... for polycystic liver diseases.
@nl
type
label
Pathophysiology, epidemiology, ...... for polycystic liver diseases
@en
Pathophysiology, epidemiology, ...... for polycystic liver diseases.
@nl
prefLabel
Pathophysiology, epidemiology, ...... for polycystic liver diseases
@en
Pathophysiology, epidemiology, ...... for polycystic liver diseases.
@nl
P2093
P2860
P356
P1476
Pathophysiology, epidemiology, ...... for polycystic liver diseases
@en
P2093
Bassam Abu-Wasel
Caolan Walsh
Michele Molinari
Valerie Keough
P2860
P304
P356
10.3748/WJG.V19.I35.5775
P407
P577
2013-09-01T00:00:00Z