Results 131 to 140 of about 266,382 (322)

Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction

Basic Research in Cardiology, 2016
Long QT syndrome is a potentially life-threatening disease characterized by delayed repolarization of cardiomyocytes, QT interval prolongation in the electrocardiogram, and a high risk for sudden cardiac death caused by ventricular arrhythmia.
D. Malan, Miao Zhang, B. Stallmeyer, J. Müller, B. Fleischmann, E. Schulze-Bahr, P. Sasse, B. Greber   +7 more
semanticscholar   +1 more source

Repotrectinib in a Patient With NTRK Fusion-Positive Pancreatic Carcinoma and Congenital Long QT Syndrome. [PDF]

Repotrectinib in a patient with NTRK fusion-positive pancreatic carcinoma and congenital long QT ...
Bazhenova, Lyudmila, Narezkina, Anna, Redfern, Charles, Velasco, Katherine, Yun, Karen, Yun, Karen   +5 more
core   +1 more source

Incidence of sudden unexpected death in epilepsy in New Zealand: A prospective population‐wide, 2‐year study

Epilepsia, EarlyView.
Abstract Objective This study was undertaken to determine the incidence of sudden unexpected death in epilepsy (SUDEP) in New Zealand. Methods We attempted to prospectively identify all people with epilepsy (PWE) in New Zealand who died from SUDEP after August 1, 2019.
Peter S. Bergin, Sunayana Sasikumar, Erica Beilharz, Charley Glenn, Robert Scragg   +4 more
wiley   +1 more source

Locus heterogeneity of autosomal dominant long QT syndrome. [PDF]

, 1993
Michael A. Curran, Donald L. Atkinson, K Timothy, G. Michael Vincent, Arthur J. Moss, M. Leppert, Mark Keating   +6 more
openalex   +1 more source

Measurement and interpretation of electrocardiographic QT intervals in murine hearts. [PDF]

, 2014
Alterations in ECG QT intervals correlate with the risk of potentially fatal arrhythmias, for which transgenic murine hearts are becoming increasingly useful experimental models. However, QT intervals are poorly defined in murine ECGs.
Fraser, James A, Huang, Christopher L-H, King, James H, Wu, JingJing, Zhang, Yanmin   +4 more
core   +2 more sources

The UMPIRE study: A first‐in‐human multicenter trial of bilateral subscalp monitoring for epileptic seizure detection

Epilepsia, EarlyView.
Abstract Objective Patient self‐report is known to be an inaccurate reflection of true seizure frequency in persons with epilepsy. The current study aimed to assess the safety and performance of the Minder system, a bilateral subscalp electroencephalographic (EEG) acquisition system for continuous long‐term EEG recording.
Amy J. Halliday, Lisa Gillinder, Alan Lai, Udaya Seneviratne, Holly Fontenot, Tracy Cameron, Karen McLean, Andrew Niemiec, Ramya Raghupathi, Taneeta M. Ganguly, Colin Ellis, Erin C. Conrad, Robert Briggs, Kristian Bulluss, Patrick Kwan, Piero Perucca, Terence J. O'Brien, Aileen McGonigal, Matthew Gutman, Jason Papacostas, Michael W. K. Fong, Andrew Lee, Douglas E. Crompton, Joshua Laing, Manori Wijayath, Andrew P. Morokoff, Michael Murphy, Wendyl J. D'Souza, Mark J. Cook   +28 more
wiley   +1 more source

Torsade de pointes and long QT syndrome following major blood transfusion [PDF]

, 1992
Padmakar M Kulkarni, Shoumo Bhattacharya, Andy Petros   +2 more
openalex   +1 more source

Long-QT Syndrome and Competitive Sports.

Arrhythmia & Electrophysiology Review, 2018
Long QT syndrome (LQTS) is an inherited channelopathy which exposes athletes to a risk of sudden cardiac death. Diagnosis is more difficult in this population because: the QT interval is prolonged by training; and the extreme bradycardia frequently ...
F. Schnell, N. Béhar, F. Carré
semanticscholar   +1 more source

Clinical Features of Brugada Syndrome Patients With SCN5A Variants

Journal of Cardiovascular Electrophysiology, EarlyView.
Longer r‐J interval in lead V1, fragmented QRS and carrying SCN5A variants other than benign variants are independently associated with the cardiac events in BrS patients. LAS40 and RMS40 are useful for the risk stratification in BrS patients with SCN5A VUS or pathogenic variants.
Sho Okamura, Hidenori Ochi, Mika Nakashima, Rie Akiyama, Takehito Tokuyama, Yousaku Okubo, Shunsuke Miyauchi, Shogo Miyamoto, Naoto Oguri, Yukimi Uotani, Takumi Sakai, Motoki Furutani, Yasuki Kihara, Yukiko Nakano   +13 more
wiley   +1 more source

Hereditary long qt syndrome in the postoperative cardiac patient [PDF]

, 1990
Thomas S. Klitzner
openalex   +1 more source