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Clinical Kidney Journal|November 10, 2021
Developing a patient-centred tool for pain measurement and evaluation in autosomal dominant polycystic kidney diseaseRagada El-Damanawi, Michael Lee, Tess Harris, et al.
Gastroenterology|December 19, 2012
Sex and age are determinants of the clinical phenotype of primary biliary cirrhosis and response to ursodeoxycholic acidMarco Carbone, George F Mells, Greta Pells, et al.
Hepatology (Baltimore, Md.)|March 9, 2013
Impact of primary biliary cirrhosis on perceived quality of life: the UK-PBC national studyGeorge F Mells, Greta Pells, Julia L Newton, et al.
Biochimica Et Biophysica Acta|December 4, 2010
Receptor protein tyrosine phosphatases are novel components of a polycystin complexCatherine A Boucher, Heather H Ward, Ruth L Case, et al.
Journal of Hepatology|March 8, 2013
The impact of liver transplantation on the phenotype of primary biliary cirrhosis patients in the UK-PBC cohortGreta Pells, George F Mells, Marco Carbone, et al.
Hepatology Communications|April 7, 2023
Regulation of immune responses in primary biliary cholangitis: a transcriptomic analysis of peripheral immune cellsVictoria Mulcahy, Evaggelia Liaskou, Jose-Ezequiel Martin, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 21, 2020
Effects of Primary Biliary Cholangitis on Quality of Life and Health Care Costs in the United KingdomStephen Rice, Viviana Albani, Dimitrios Minos, et al.
BMJ Open|June 15, 2022
Research priorities for autosomal dominant polycystic kidney disease: a UK priority setting partnershipTess Harris, Hannah R Bridges, Wendy D Brown, et al.
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