Results 151 to 160 of about 169,795 (221)

Apparent Ventricular Bigeminy in the Congenital Long QT Syndrome: What is the Mechanism? [PDF]

, 2000
Yen‐Bin Liu, Wen‐Jone Chen, Yuan‐Teh Lee   +2 more
openalex   +1 more source

Integration of validated functional evidence to support the pathogenicity of KCNH2 variants

Genetics in Medicine Open
Functional investigation of genetic variants found in long QT syndrome can provide evidence that is needed to confirm the genetic diagnosis and establish the cause of the condition.
Reema W. Aljassar, Qianyi Shen, Buthaina Albash, Jamie I. Vandenberg, Mohammad A. Ebrahim, Chai-Ann Ng   +5 more
doaj  

Acute Hypokalemia May Not Be an Effective Way to Sensitize the In Situ Canine Heart for Sparfloxacin-Induced Long QT Syndrome

Journal of Pharmacological Sciences, 2006
.: Extents of the sparfloxacin (3 – 10 mg/kg, i.v.)-induced QT interval prolongation under normokalemic and hypokalemic conditions were assessed in halothane-anesthetized beagle dogs (n = 5).
Katsuyoshi Chiba, Atsushi Sugiyama, Kazuo Watanabe, Kiyoshi Takasuna, Keitaro Hashimoto   +4 more
doaj  

Effectiveness and Limitations of β-Blocker Therapy in Congenital Long-QT Syndrome [PDF]

, 2000
Arthur J. Moss, Wojciech Zaręba, William J. Hall, Peter J. Schwartz, Richard S. Crampton, Jesaia Benhorin, G. Michael Vincent, Emanuela H. Locati, Silvia G. Priori, Carlo Napolitano, Aharon Medina, Li Zhang, Jennifer L. Robinson, Katherine W. Timothy, Jeffrey A. Towbin, Mark Andrews   +15 more
openalex   +1 more source

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.

, 1997
John Burn, A. John Camm, Melanie J. Davies, L. Peltonen, Peter J. Schwartz, Hugh Watkins   +5 more
openalex   +1 more source

A structural basis for drug-induced long QT syndrome [PDF]

, 2000
John S. Mitcheson, Jun Chen, Monica Lin, Chris Culberson, Michael C. Sanguinetti   +4 more
openalex   +1 more source

Mutation of the Gene for I sK Associated With Both Jervell and Lange-Nielsen and Romano-Ward Forms of Long-QT Syndrome

, 1998
Priya Duggal, Mark R. Vesely, Duangrurdee Wattanasirichaigoon, Juan Villafañe, Vineet Kaushik, Alan H. Beggs   +5 more
openalex   +1 more source

Arrhythmias in the congenital long QT syndrome: how often is torsade de pointes pause dependent? [PDF]

, 2000
Sami Viskin
openalex   +1 more source

Electrocardiographic parameter profiles for differentiating hypertrophic cardiomyopathy stages

Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
Our findings revealed that ST‐T segment parameters were especially significant for diagnosing HCM, with similar weight across the basal and apical subtypes. In contrast, QRS complex parameters were more pertinent for diagnosing dHCM, suggesting a shift in diagnostic emphasis as the disease progresses.
Naomi Hirota, Shinya Suzuki, Takuto Arita, Naoharu Yagi, Mikio Kishi, Hiroaki Semba, Hiroto Kano, Shunsuke Matsuno, Yuko Kato, Takayuki Otsuka, Junji Yajima, Tokuhisa Uejima, Yuji Oikawa, Takeshi Yamashita   +13 more
wiley   +1 more source

Observations on the onset of Torsade de Pointes arrhythmias in the acquired long QT syndrome [PDF]

, 2000
Marc A. Vos
openalex   +1 more source