Showing results (11-20 of 14) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.Journal of Hepatology|March 20, 2004
The impact of peginterferon alfa-2a plus ribavirin combination therapy on health-related quality of life in chronic hepatitis CTarek Hassanein, Graham Cooksley, Mark Sulkowski, et al.Journal of Medical Genetics|January 1, 1995
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysisR H Boerman, R A Ophoff, T P Links, et al.United European Gastroenterology Journal|June 8, 2021
Predictors for incomplete response to ursodeoxycholic acid in primary biliary cholangitis. Data from a national registry of liver diseaseHelena Cortez-Pinto, Rodrigo Liberal, Susana Lopes, et al.Pageof 2