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

Minoru Horie

Showing results (351-360 of 428) with videos related to

Pageof 43
Sort By:
The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.
Circulation. Cardiovascular Genetics|May 17, 2012
Phenotype variability in patients carrying KCNJ2 mutationsHiromi Kimura, Jun Zhou, Mihoko Kawamura, et al.
Circulation. Arrhythmia and Electrophysiology|September 16, 2014
Electrical storm in patients with brugada syndrome is associated with early repolarizationYoshiaki Kaneko, Minoru Horie, Shinichi Niwano, et al.
European Heart Journal|December 31, 2015
The genetics underlying acquired long QT syndrome: impact for genetic screeningHideki Itoh, Lia Crotti, Takeshi Aiba, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|April 19, 2013
Genetic background of catecholaminergic polymorphic ventricular tachycardia in JapanMihoko Kawamura, Seiko Ohno, Nobu Naiki, et al.
Heart (British Cardiac Society)|February 9, 2022
Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1Keiko Shimamoto, Seiko Ohno, Koichi Kato, et al.
Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Long-term prognosis of probands with Brugada-pattern ST-elevation in leads V1-V3Shiro Kamakura, Tohru Ohe, Kiyoshi Nakazawa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2022
Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathiesMatthew J O'Neill, Luca Sala, Isabelle Denjoy, et al.
Circulation. Arrhythmia and Electrophysiology|December 10, 2009
Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in JapanHitoshi Horigome, Masami Nagashima, Naokata Sumitomo, et al.
Plos One|October 21, 2016
Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular TachycardiaKenichi Sasaki, Takeru Makiyama, Yoshinori Yoshida, et al.
Pageof 43

Showing results (351-360 of 428) with videos related to

Sort By:
Pageof 43
The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.
Circulation. Cardiovascular Genetics|May 17, 2012
Phenotype variability in patients carrying KCNJ2 mutationsHiromi Kimura, Jun Zhou, Mihoko Kawamura, et al.
Circulation. Arrhythmia and Electrophysiology|September 16, 2014
Electrical storm in patients with brugada syndrome is associated with early repolarizationYoshiaki Kaneko, Minoru Horie, Shinichi Niwano, et al.
European Heart Journal|December 31, 2015
The genetics underlying acquired long QT syndrome: impact for genetic screeningHideki Itoh, Lia Crotti, Takeshi Aiba, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|April 19, 2013
Genetic background of catecholaminergic polymorphic ventricular tachycardia in JapanMihoko Kawamura, Seiko Ohno, Nobu Naiki, et al.
Heart (British Cardiac Society)|February 9, 2022
Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1Keiko Shimamoto, Seiko Ohno, Koichi Kato, et al.
Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Long-term prognosis of probands with Brugada-pattern ST-elevation in leads V1-V3Shiro Kamakura, Tohru Ohe, Kiyoshi Nakazawa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2022
Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathiesMatthew J O'Neill, Luca Sala, Isabelle Denjoy, et al.
Circulation. Arrhythmia and Electrophysiology|December 10, 2009
Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in JapanHitoshi Horigome, Masami Nagashima, Naokata Sumitomo, et al.
Plos One|October 21, 2016
Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular TachycardiaKenichi Sasaki, Takeru Makiyama, Yoshinori Yoshida, et al.
Pageof 43