نتایج جستجو برای: long qt سندرم

تعداد نتایج: 790950  

Journal: :JACC: Clinical Electrophysiology 2018

Journal: :Health Education and Care 2019

Journal: :European Heart Journal 2000

Journal: :Medicina Universitaria 2015

2011
Kinge van der Heide Ann de Haes Götz JK Wietasch Ans CP Wiesfeld Herman GD Hendriks

INTRODUCTION Torsades de pointes is a rare but potentially lethal arrhythmia. The amount of literature available on Torsades de pointes occurring in patients with pheochromocytoma is limited, and we found no literature describing this dysrhythmia in a patient with pheochromocytoma under anesthesia. CASE PRESENTATION We describe the case of a 42-year-old Caucasian woman without QT prolongation...

Journal: :Circulation journal : official journal of the Japanese Circulation Society 2003
Masaru Inoue Masami Shimizu Hidekazu Ino Masato Yamaguchi Hidenobu Terai Kenshi Hayashi Masaru Kiyama Kenji Sakata Tatsumi Hayashi Hiroshi Mabuchi

Congenital long QT syndrome (LQTS) is caused by mutations in various cardiac potassium or sodium channel genes, with 6 different genotypes thus far identified. However, it is unknown whether these genotypes can be differentiated by QT variables. The electrocardiograms obtained from 16 patients with a mutation in KCNQ1 (LQT1), 7 patients with a mutation in HERG (LQT2) and 20 control subjects wer...

Journal: :Circulation 2007
Mohan N Viswanathan Richard L Page

For half a century, the relationship between the QT interval and cardiac arrhythmias has been recognized,1 although attention has focused primarily on prolongation of the QT. The congenital long-QT syndrome (LQTS) was first identified in patients with syncope, aborted sudden death, or family history of cardiac arrest as an association between a prolonged QT interval and development of potential...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید