The long QT syndrome
AJ Moss, W Zarebra, JL Robinson - Cardiology in Review, 1995 - journals.lww.com
The primary form of long QT syndrome (LQTS) is an infrequently occuring familial disorder in
which affected members have electrocardiographic QT interval prolongation and a …
which affected members have electrocardiographic QT interval prolongation and a …
[引用][C] Clinical Aspects of the Idiopathic Long QT Syndrome a
AJ Moss, JL Robinson - Annals of the New York Academy of …, 1992 - Wiley Online Library
The idiopathic Long QI' Syndrome (LWS) is an infrequently occurring disorder in which
affected family members have an unusual electrocardiographic repolarization abnormality …
affected family members have an unusual electrocardiographic repolarization abnormality …
Clinical and therapeutic aspects of congenital and acquired long QT syndrome
IA Khan - The American journal of medicine, 2002 - Elsevier
The long QT syndrome is characterized by prolongation of the corrected QT (QTc) interval on
the surface electrocardiogram. It is associated with precipitation of a polymorphic ventricular …
the surface electrocardiogram. It is associated with precipitation of a polymorphic ventricular …
Clinical features of the idiopathic long QT syndrome.
AJ Moss, J Robinson - Circulation, 1992 - europepmc.org
Long QT syndrome (LQTS) is an infrequently occurring familial disorder in which affected
members have electrocardiographic QT interval prolongation and a propensity to syncope …
members have electrocardiographic QT interval prolongation and a propensity to syncope …
[引用][C] The long QT syndrome revisited: current understanding and implications for treatment
AJ Moss - Pacing and clinical electrophysiology, 1997 - Wiley Online Library
The hereditary long QT syndrome (LQTS] is an uncommon disorder in which affected
individuals have QT prolongation and a propensity to syncope, polymorphous ventricular …
individuals have QT prolongation and a propensity to syncope, polymorphous ventricular …
Ventricular tachyarrhythmias in the long QT syndromes
WM Jackman, M Clark, KJ Friday, EM Aliot… - Medical Clinics of North …, 1984 - Elsevier
Marked prolongation of the electrocardiographic QT (or QTU) interval often is associated
with a distinctive form of ventricular tachycardia characterized by the gradual oscillation …
with a distinctive form of ventricular tachycardia characterized by the gradual oscillation …
The long QT syndrome. Prospective longitudinal study of 328 families.
AJ Moss, PJ Schwartz, RS Crampton, D Tzivoni… - Circulation, 1991 - Am Heart Assoc
BACKGROUND The Long QT Syndrome (LQTS) is an infrequently occurring familial
disorder in which affected individuals have electrocardiographic QT interval prolongation …
disorder in which affected individuals have electrocardiographic QT interval prolongation …
Congenital long QT syndrome.
N Ahmed, K Riaz, R Rai, M Osman… - Reviews in …, 2006 - europepmc.org
Long QT syndrome (LQTS) can be asymptomatic-identifiable as an incidental finding on
electrocardiogram-or it can present with palpitation, syncope, seizures, or sudden cardiac …
electrocardiogram-or it can present with palpitation, syncope, seizures, or sudden cardiac …
Long QT syndrome: first and fatal events provoked by hemodialysis
RF Miller, MW Haley, L Littmann - Pacing and clinical …, 2003 - Wiley Online Library
MILLER, RF, et al.: Long QT Syndrome: First and Fatal Events Provoked by Hemodialysis.
Long QT syndrome (LQTS) involves both congenital and acquired predispositions toward …
Long QT syndrome (LQTS) involves both congenital and acquired predispositions toward …
[引用][C] Congenital long QT syndrome
GM Vincent, K Timothy, L Zhang - Cardiac Electrophysiology Review, 1997 - Springer
The inherited long QT syndrome (LQTS) has been identified in essentially all races and
ethnic groups. It is unknown if there are differences in prevalence in specific races or ethnic …
ethnic groups. It is unknown if there are differences in prevalence in specific races or ethnic …