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Cardiac Electrophysiology Clinics, 2010
The short QT syndrome is a recently described genetic arrhythmogenic disorder, characterized by abnormally short QT intervals and a high incidence of sudden death and atrial fibrillation. Clinical manifestations may also be present in infants; a family history of cardiac sudden death is often present.
GAITA, Fiorenzo +2 more
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The short QT syndrome is a recently described genetic arrhythmogenic disorder, characterized by abnormally short QT intervals and a high incidence of sudden death and atrial fibrillation. Clinical manifestations may also be present in infants; a family history of cardiac sudden death is often present.
GAITA, Fiorenzo +2 more
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2021
The short QT syndrome (SQTS) is a rare cardiac ion channel disease predisposing to ventricular arrhythmias (VAs) and sudden cardiac death (SCD) in the young [1]. The signature feature of SQTS is the presence of a constantly short QT interval at ECG in the absence of structural cardiac abnormalities. First described in 2000 [2], SQTS was recognised as a
Chiara Scrocco +2 more
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The short QT syndrome (SQTS) is a rare cardiac ion channel disease predisposing to ventricular arrhythmias (VAs) and sudden cardiac death (SCD) in the young [1]. The signature feature of SQTS is the presence of a constantly short QT interval at ECG in the absence of structural cardiac abnormalities. First described in 2000 [2], SQTS was recognised as a
Chiara Scrocco +2 more
openaire +1 more source
2019
The short QT syndrome (SQTS) is a rare inherited ion channel disease associated with life-threatening arrhythmias and familiar sudden death (SD) in the absence of cardiac structural abnormalities. The diagnosis is based on the detection of constantly short QTc values at ECG (≤ 340 ms) and the presence of previous aborted CA (aCA) or syncope, a family ...
Chiara Scrocco +2 more
openaire +2 more sources
The short QT syndrome (SQTS) is a rare inherited ion channel disease associated with life-threatening arrhythmias and familiar sudden death (SD) in the absence of cardiac structural abnormalities. The diagnosis is based on the detection of constantly short QTc values at ECG (≤ 340 ms) and the presence of previous aborted CA (aCA) or syncope, a family ...
Chiara Scrocco +2 more
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2016
The short QT syndrome is defined, and recommendations for management of these patients are provided.
Demosthenes G. Katritsis +2 more
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The short QT syndrome is defined, and recommendations for management of these patients are provided.
Demosthenes G. Katritsis +2 more
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Herzschrittmachertherapie & Elektrophysiologie, 2006
In the past decade molecular genetic analysis has greatly expanded our knowledge about inherited arrhythmogenic syndromes. The congenital long QT syndrome (LQTS) and the recently described short QT syndrome (SQTS), with the defining characteristic of abnormal prolongation or shortening of the QTc interval on the surface electrocardiogram, are caused by
B, Borchert, T, Lawrenz, C, Stellbrink
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In the past decade molecular genetic analysis has greatly expanded our knowledge about inherited arrhythmogenic syndromes. The congenital long QT syndrome (LQTS) and the recently described short QT syndrome (SQTS), with the defining characteristic of abnormal prolongation or shortening of the QTc interval on the surface electrocardiogram, are caused by
B, Borchert, T, Lawrenz, C, Stellbrink
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Channelopathies: Brugada syndrome, long QT syndrome, short QT syndrome, and CPVT
Herz, 2009In approximately 10-20% of all sudden deaths, no structural cardiac abnormalities can be identified. Important potential causes of sudden cardiac deaths in the absence of heart disease are primary electrical diseases such as Brugada syndrome, long QT syndrome (LQTS), short QT syndrome (SQTS), and catecholaminergic polymorphic ventricular ...
Rainer, Schimpf +3 more
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2018
The long and short QT syndromes are genetically transmitted arrhythmogenic diseases characterized by an abnormal QTc on the basal ECG and by an increased risk of life-threatening arrhythmias. While in the long QT syndrome well-established diagnostic criteria are available as well as effective treatments, in the short QT syndrome, much less is known in ...
Crotti, L, Kotta, MK, Castelletti, S.
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The long and short QT syndromes are genetically transmitted arrhythmogenic diseases characterized by an abnormal QTc on the basal ECG and by an increased risk of life-threatening arrhythmias. While in the long QT syndrome well-established diagnostic criteria are available as well as effective treatments, in the short QT syndrome, much less is known in ...
Crotti, L, Kotta, MK, Castelletti, S.
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Brugada and Short QT Syndromes
Pacing and Clinical Electrophysiology, 2009Brugada syndrome and short QT syndrome are among the rarer cardiac channelopathies that may result in sudden cardiac arrest. The genetics and molecular mechanisms of these diseases provide insight into the mechanisms of more common channelopathies, and may dictate special therapeutic approaches with respect to drug therapy and risk stratification.
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Targeted therapy for short QT syndrome
Expert Opinion on Therapeutic Targets, 2006Identified in 2000, short QT syndrome is an electrical disease of the heart characterised as a channelopathy. At first considered extremely rare, families with this disease have been found in Brazil, Finland, Germany, Spain, the Netherlands, France, Turkey, Italy and the US. The focus of the paper is to present a current review of short QT syndrome, as
Preben, Bjerregaard +2 more
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