Results 201 to 210 of about 138,611 (238)
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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

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 syndrome autosomal dominant in three generations

American Journal of Medical Genetics, 1999
Andersen syndrome is a rare entity and comprises potassium sensitive periodic paralysis, ventricular arrhythmia, and an unusual facial appearance; syncope and sudden death have also been reported. The recognition of the characteristic face permits an early diagnosis in order to detect the severe systemic manifestations that are associated with this ...
S, Canún, N, Pérez, L G, Beirana
openaire   +2 more sources

Andersen-Tawil and Timothy Syndromes

2013
This chapter summarizes two relatively new ion channelopathies, Andersen-Tawil and Timothy syndromes. Both disorders are pleiotropic in nature, with multiple clinical manifestations outside the cardiovascular system. While both Andersen-Tawil and Timothy syndromes are disorders of ventricular repolarization, their unique clinical phenotype ...
Martin Tristani-Firouzi   +1 more
openaire   +1 more source

Andersen–Tawil syndrome. A diagnostic challenge

International Journal of Cardiology, 2016
Article history: Received 14 November 2015 Accepted 22 November 2015 Available online 26 November 2015 heart sounds by premature beats with compensatory pause. Holter monitoring reported corrected QT interval of 515 ms, and very frequent VPB (32,231/24 h), with multiple morphologies, couplets, bigeminy, and trigeminy.
Martha Abigaíl Reyes Villatoro   +5 more
openaire   +1 more source

Andersen-Tawil syndrome

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

Andersen–Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity

Brain, 2022
Vinojini Vivekanandam   +2 more
exaly  

Andersen Syndrome

2009
Hubert Scharnagl   +199 more
openaire   +1 more source

Clinical heterogeneity in Andersen-Tawil syndrome

Neuromuscular Disorders, 2017
Armando, Totomoch-Serra   +2 more
openaire   +2 more sources

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