Results 151 to 160 of about 20,847 (184)
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Coexistent manifestations of the Andersen-Tawil and Brugada syndromes

Journal of Electrocardiology, 2008
The Andersen-Tawil syndrome (ATS) is a rare inherited disorder characterized by periodic paralysis, ventricular arrhythmias, skeletal developmental abnormalities, and in most cases, prolongation of the QT interval (or more correctly, the QU interval).
Adrian H, Shandling, Michael, Safani
openaire   +2 more sources

Andersen–Tawil Syndrome With Early Fixed Myopathy

Journal of Clinical Neuromuscular Disease, 2014
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant potassium channelopathy characterized by a triad of periodic paralysis, ventricular arrhythmias, and distinctive dysmorphic abnormalities. We present a 19-year-old man with characteristic skeletal dysmorphic features of ATS, early nonfluctuating proximal lower limb weakness from childhood, and ...
Stela, Lefter   +6 more
openaire   +2 more sources

Clinical and neurophysiological variability in Andersen‐Tawil syndrome

Muscle & Nerve, 2019
AbstractIntroductionAndersen‐Tawil syndrome (ATS) is characterized by a triad of periodic paralysis, ventricular arrhythmias, and dysmorphism. However, patients often lack one or more of these features.MethodsClinical and neurophysiological features were reviewed of five members in two families with heterozygous mutations in KCNJ2 (R218Q and R67W ...
Norito, Kokubun   +6 more
openaire   +2 more sources

Kir 2.1 channelopathies: the Andersen–Tawil syndrome

Pflügers Archiv - European Journal of Physiology, 2010
As a multisystem disorder, Andersen-Tawil syndrome (ATS) is rather unique in the family of channelopathies. The full spectrum of the disease is characterized by ventricular arrhythmias, dysmorphic features, and periodic paralysis. Most ATS patients have a mutation in the ion channel gene, KCNJ2, which encodes the inward rectifier K+ channel Kir2.1, a ...
Martin, Tristani-Firouzi   +1 more
openaire   +2 more sources

Andersen-Tawil syndrome

Drugs of the Future, 2008
null Dulsat, C., null Mealy, N.
openaire   +1 more source

Andersen Syndrome

2009
Hubert Scharnagl   +199 more
openaire   +1 more source

Efficacy of flecainide in bidirectional ventricular tachycardia and tachycardia-induced cardiomyopathy with Andersen-Tawil syndrome

European Journal of Medical Genetics, 2022
Gülen Eda Utine   +2 more
exaly  

Obstetric management of a patient with Andersen–Tawil syndrome: A case report

Journal of Obstetrics and Gynaecology Research, 2021
Naoyuki Miyasaka   +2 more
exaly  

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