Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Bathen

Showing results (21-30 of 26) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 26 results.
Journal of Electrocardiology|January 10, 2002
T-wave morphology differences between patients with and without arrhythmic complication of ischemic heart diseaseK Hnatkova, S J Ryan, J Bathen, et al.
Clinical Chemistry|July 27, 2001
Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndromeL A Larsen, P S Andersen, J Kanters, et al.
Circulation|October 1, 1984
Evolution of infarct size during the early use of nifedipine in patients with acute myocardial infarction: the Norwegian Nifedipine Multicenter TrialP A Sirnes, K Overskeid, T R Pedersen, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Acta Neurologica Scandinavica. Supplementum|January 5, 2001
Familial mydriasis, cardiac arrhythmia, respiratory failure, muscular weakness and hypohidrosisO Sjaastad, C F Lindboe, J Schaanning, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Journal of Electrocardiology|January 10, 2002
T-wave morphology differences between patients with and without arrhythmic complication of ischemic heart diseaseK Hnatkova, S J Ryan, J Bathen, et al.
Clinical Chemistry|July 27, 2001
Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndromeL A Larsen, P S Andersen, J Kanters, et al.
Circulation|October 1, 1984
Evolution of infarct size during the early use of nifedipine in patients with acute myocardial infarction: the Norwegian Nifedipine Multicenter TrialP A Sirnes, K Overskeid, T R Pedersen, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Acta Neurologica Scandinavica. Supplementum|January 5, 2001
Familial mydriasis, cardiac arrhythmia, respiratory failure, muscular weakness and hypohidrosisO Sjaastad, C F Lindboe, J Schaanning, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Pageof 3