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Polycystic Liver Diseases

2020
Polycystic liver disease is a rare disease, manifesting with progressive bile duct enlargement and development of multiple cysts of various sizes in the liver. While it can be regarded as a hereditary disease, with either autosomal dominant transmission or autosomal recessive transmission, only about 20% of patients have been identified to have genetic
Carmen Fierbinteanu-Braticevici   +1 more
openaire   +1 more source

Polycystic Disease of the Liver

JAMA: The Journal of the American Medical Association, 1971
Polycystic liver disease usually presents as a benign progressive hepatomegaly, the true characteristic of which is found during surgical exploration or at postmortem examination. Liver function tests, biopsies, and scans are of little value diagnostically.
openaire   +1 more source

POLYCYSTIC DISEASE OF THE LIVER

Australian and New Zealand Journal of Surgery, 1953
N, WADDLE, R, RODDA
openaire   +2 more sources

Polycystic Liver and Kidney Disease

Clinical Gastroenterology and Hepatology, 2022
Kwabena Oware, Adu-Gyamfi   +2 more
openaire   +2 more sources

Polycystic liver disease

Journal of Clinical Ultrasound, 1978
C C, Kuni, M L, Johnson, J H, Holmes
openaire   +2 more sources

Liver Transplantation for Polycystic Liver Disease

Journal of the American College of Surgeons, 2014
Daniel, Zamora-Valdés   +2 more
openaire   +2 more sources

Predicting liver cyst severity by mutations in patients with autosomal-dominant polycystic kidney disease

Hepatology International, 2021
Hiroshi Kataoka   +2 more
exaly  

Disparities in liver cancer occurrence in the United States by race/ethnicity and state

Ca-A Cancer Journal for Clinicians, 2017
Rebecca L. Siegel   +2 more
exaly  

Novel causative genes for polycystic liver disease

Nature Reviews Gastroenterology and Hepatology, 2017
Jesus M Banales, María J Perugorria
exaly  

New insights into targeting hepatic cystogenesis in autosomal dominant polycystic liver and kidney disease

Expert Opinion on Therapeutic Targets, 2020
Tom J G Gevers, Lucas H P Bernts
exaly  

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