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Heart Rhythm
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March 23, 2011
Nonsense-mediated mRNA decay caused by a frameshift mutation in a large kindred of type 2 long QT syndrome
Ignatius Gerardo Zarraga, Li Zhang, Matthew R Stump, et al.
BMC Medical Genetics
|
September 24, 2008
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations
Xianqin Zhang, Shenghan Chen, Li Zhang, et al.
Journal of Molecular and Cellular Cardiology
|
February 15, 2008
A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome
Qiuming Gong, Li Zhang, Arthur J Moss, et al.
Journal of the American College of Cardiology
|
September 5, 2006
Corrected QT variability in serial electrocardiograms in long QT syndrome: the importance of the maximum corrected QT for risk stratification
Ilan Goldenberg, Jehu Mathew, Arthur J Moss, et al.
Circulation
|
January 2, 2009
High efficacy of beta-blockers in long-QT syndrome type 1: contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment "failures"
G Michael Vincent, Peter J Schwartz, Isabelle Denjoy, et al.
Journal of the American College of Cardiology
|
September 15, 2004
An intronic mutation causes long QT syndrome
Li Zhang, G Michael Vincent, Marco Baralle, et al.
American Heart Journal
|
August 9, 2005
Improved long-term survival associated with stent deployment during percutaneous coronary interventions: results from a registry of 3399 patients
Joseph B Muhlestein, Jeffrey L Anderson, ChangZong Cui, et al.
Circulation
|
May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype
Li Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Circulation. Cardiovascular Genetics
|
August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation
Alon Barsheshet, Arthur J Moss, Scott McNitt, et al.
Journal of Cardiovascular Electrophysiology
|
December 18, 2003
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome
Wojciech Zareba, Arthur J Moss, Gloria Sheu, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Heart Rhythm
|
March 23, 2011
Nonsense-mediated mRNA decay caused by a frameshift mutation in a large kindred of type 2 long QT syndrome
Ignatius Gerardo Zarraga, Li Zhang, Matthew R Stump, et al.
BMC Medical Genetics
|
September 24, 2008
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations
Xianqin Zhang, Shenghan Chen, Li Zhang, et al.
Journal of Molecular and Cellular Cardiology
|
February 15, 2008
A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome
Qiuming Gong, Li Zhang, Arthur J Moss, et al.
Journal of the American College of Cardiology
|
September 5, 2006
Corrected QT variability in serial electrocardiograms in long QT syndrome: the importance of the maximum corrected QT for risk stratification
Ilan Goldenberg, Jehu Mathew, Arthur J Moss, et al.
Circulation
|
January 2, 2009
High efficacy of beta-blockers in long-QT syndrome type 1: contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment "failures"
G Michael Vincent, Peter J Schwartz, Isabelle Denjoy, et al.
Journal of the American College of Cardiology
|
September 15, 2004
An intronic mutation causes long QT syndrome
Li Zhang, G Michael Vincent, Marco Baralle, et al.
American Heart Journal
|
August 9, 2005
Improved long-term survival associated with stent deployment during percutaneous coronary interventions: results from a registry of 3399 patients
Joseph B Muhlestein, Jeffrey L Anderson, ChangZong Cui, et al.
Circulation
|
May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype
Li Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Circulation. Cardiovascular Genetics
|
August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation
Alon Barsheshet, Arthur J Moss, Scott McNitt, et al.
Journal of Cardiovascular Electrophysiology
|
December 18, 2003
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome
Wojciech Zareba, Arthur J Moss, Gloria Sheu, et al.
Page
of 4