Results 11 to 20 of about 20,149 (199)

Short QT syndrome [PDF]

open access: yesCardiogenetics, 2011
The short QT syndrome (SQTS) is a recently described genetic arrhythmogenic disorder, characterized by abnormally short QT intervals on surface electrocardiogram (ECG) and a high incidence of sudden death (SD) during life, including the first months of ...
Fiorenzo Gaita   +4 more
doaj   +10 more sources

Congenital Short QT Syndrome

open access: yesIndian Pacing and Electrophysiology Journal, 2004
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital long QT syndrome was first described in individuals with structurally normal hearts in 1957.1 Little was known about the significance of a short QT ...
Charles Antzelevitch, Johnson Francis
doaj   +2 more sources

Short QT syndrome [PDF]

open access: yesCanadian Medical Association Journal, 2005
The QT interval on an electrocardiogram signifies the time required for the heart to repolarize after depolarization. It has long been appreciated that a long QT interval predisposes patients to life-threatening ventricular arrhythmia. Short QT syndrome is a newly described disease characterized by a shortened QT interval and by episodes of syncope ...
Ramon, Brugada   +3 more
  +12 more sources

Short QT interval syndrome

open access: yesКардиоваскулярная терапия и профилактика, 1970
Every year, sudden cardiac death (SCD) takes lives of 400 000 American citizens, and in 10-20% ofthe cases, fatal outcome is explained by hereditary pathology.
I. G. Fomina   +2 more
doaj   +1 more source

Phase Ib study of anlotinib combined with TQB2450 in pretreated advanced biliary tract cancer and biomarker analysis

open access: yesHepatology, EarlyView., 2022
Phase 1b study of anlotinib combined with TQB2450 in pretreated advanced biliary tract cancer and biomarker analysis. Abstract Background and Aims We evaluated the efficacy and safety of the antiangiogenic tyrosine kinase inhibitor anlotinib plus TQB2450, a programmed death‐ligand 1 inhibitor in pretreated advanced biliary tract cancers (BTCs ...
Jun Zhou   +13 more
wiley   +1 more source

Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population

open access: yesBiomedicines, 2022
Sudden death is a rare event in the pediatric population but with a social shock due to its presentation as the first symptom in previously healthy children. Comprehensive autopsy in pediatric cases identify an inconclusive cause in 40–50% of cases.
Estefanía Martínez-Barrios   +9 more
doaj   +1 more source

Long QT syndrome - causes and risk factors

open access: yesJournal of Education, Health and Sport, 2018
Sudden cardiac death is a major public health challenge, which can be caused by genetic or acquired structural or electrophysiological abnormalities. These abnormalities include channelopathies such as long QT, short QT and Brugada syndromes.
Erwin Ciechański   +3 more
doaj   +3 more sources

The dark side of the QT interval. The Short QT Syndrome: pathophysiology, clinical presentation and management

open access: yesEmergency Care Journal, 2012
A large number of studies has been carried out to investigate the pathophysiology and the clinical implications of QT interval prolongation in the ECG over recent years (1, 2, 3, 4, 5, 6). It was only in the last decade, however, that the scientists have
I. Comelli   +6 more
doaj   +1 more source

Mechanisms, Risk Factors, and Management of Acquired Long QT Syndrome: A Comprehensive Review

open access: yesThe Scientific World Journal, 2012
Long QT syndrome is characterized by prolongation of the corrected QT (QTc) interval on the surface electrocardiogram and is associated with precipitation of torsade de pointes (TdP), a polymorphic ventricular tachycardia that may cause sudden death ...
Eleftherios M. Kallergis   +4 more
doaj   +1 more source

Short QT syndrome presenting as syncope: How short is too short?

open access: yesRevista Portuguesa de Cardiologia, 2014
We report the case of a 52-year-old man who presented to our emergency department (ED) after three episodes of syncope in the seven hours before admission.
Guilherme Portugal   +7 more
doaj   +1 more source

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