Results 131 to 140 of about 4,944 (184)

Different responses to exercise between Andersen–Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia

Europace, 2018
Y. Inoue, T. Aiba, H. Kawata, T. Sakaguchi, W. Mitsuma, H. Morita, T. Noda, H. Takaki, K. Toyohara, Yoshiaki Kanaya, T. Itoi, T. Mitsuhashi, N. Sumitomo, Yongkeun Cho, S. Yasuda, S. Kamakura, K. Kusano, Y. Miyamoto, M. Horie, W. Shimizu   +19 more
semanticscholar   +1 more source

Andersen-Tawil Syndrome and Hypothyroidism: A Case Report with an Unusual Association.

Int J Appl Basic Med Res, 2019
Saalim M, Karjodkar FR, Sansare KP, Sharma SR.   +3 more
europepmc   +1 more source

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

Arch Med Sci, 2018
Bienias P, Kostera-Pruszczyk A, Miszczak-Knecht M, Ciurzyński M, Pruszczyk P.   +4 more
europepmc   +1 more source

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

Ann Noninvasive Electrocardiol, 2014
Hayashi H, Kawaguchi T, Horie M.
europepmc   +1 more source

Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene. [PDF]

J Cardiol, 2017
Krych M, Biernacka EK, Ponińska J, Kukla P, Filipecki A, Gajda R, Hasdemir C, Antzelevitch C, Kosiec A, Szperl M, Płoski R, Trusz-Gluza M, Mizia-Stec K, Hoffman P.   +13 more
europepmc   +1 more source

Andersen-Tawil syndrome (ATS) – Case report and literature review

Journal of Pre-Clinical and Clinical Research, 2015
Katarzyna Olszewska, Jerzy Błaszczak, Maria Mielnik-Błaszczak   +2 more
openaire   +1 more source

Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family. [PDF]

Ann Noninvasive Electrocardiol, 2016
Jagodzińska M, Szperl M, Ponińska J, Kosiec A, Gajda R, Kukla P, Biernacka EK.   +6 more
europepmc   +1 more source

Novel mutation in the KCNJ2 gene is associated with a malignant arrhythmic phenotype of Andersen-Tawil syndrome. [PDF]

Ann Noninvasive Electrocardiol, 2013
Fernlund E, Lundin C, Hertervig E, Kongstad O, Alders M, Platonov P.   +5 more
europepmc   +1 more source

Clinical and genetic analysis of rare ion channel diseases [PDF]

Borbás János
core  

Signature ECG part 4: A 6 year-old with an irregular pulse. [PDF]

Indian Pacing Electrophysiol J
Wilde AA, Chockalingam P.
europepmc   +1 more source