Results 101 to 110 of about 860 (142)

Propafenone is not effective for severe ventricular arrhythmias in Andersen-Tawil syndrome. [PDF]

open access: yesArch Med Sci, 2018
Bienias P   +4 more
europepmc   +1 more source

Effect of flecainide on T-wave alternans in Andersen-Tawil syndrome. [PDF]

open access: yesAnn Noninvasive Electrocardiol, 2014
Hayashi H, Kawaguchi T, Horie M.
europepmc   +1 more source

Extreme prolongation of QTU in a patient with Andersen–Tawil syndrome

open access: yesPolish Heart Journal
Elżbieta Katarzyna, Biernacka   +2 more
openaire   +2 more sources

Andersen-Tawil syndrome

International Journal of Cardiology, 2011
Advances in the understanding of genetic aspects of cardiovascular diseases, together with an increase in the availability of genetic analysis, have resulted in not only increased diagnosis of known inherited conditions, but also the identification of novel syndromes.
Robin A P Weir, Victoria Murday
exaly   +2 more sources

Andersen–Tawil syndrome: Clinical and molecular aspects

International Journal of Cardiology, 2013
Andersen–Tawil syndrome (ATS) is a rare hereditary multisystem disorder. Ventricular arrhythmias, periodic paralysis and dysmorphic features constitute the classic triad of ATS symptoms. The expressivity of these symptoms is, however, extremely variable, even within single ATS affected families, and not all ATS patients present with the full triad of ...
Ronald Wilders
exaly   +3 more sources

Cardiac Surgery for a Patient With Andersen-Tawil Syndrome

The Annals of Thoracic Surgery, 2010
Andersen-Tawil syndrome is an uncommon inherited autosomal disorder characterized by a prolonged QT interval, periodic paralysis, and dysmorphic features. The deleterious effects of cardioplegia on periodic paralysis and cardiac arrhythmia are unknown, and no studies have reported the performance of cardiac surgery in patients with Andersen-Tawil ...
Mitsugi, Nagashima   +3 more
openaire   +2 more sources

Andersen-Tawil syndrome

Andersen-Tawil syndrome (ATS) is one of the periodic paralyses, a set of skeletal muscle disorders that cause transient weakness of the arms and legs lasting minutes to many hours. Distinguishing features of ATS include facial and limb dysmorphisms, cardiac arrhythmia, difficulties with executive function, and association with dominant mutations in the
Jill A, Goslinga   +3 more
openaire   +2 more sources

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