Results 131 to 140 of about 9,985 (188)

Channelopathy linking <i>KCNH2</i> mutation and primary aldosteronism: a case of life-threatening torsades de pointes. [PDF]

open access: yesJCEM Case Rep
Dejprapasorn S   +5 more
europepmc   +1 more source

Familial Short QT Syndrome: Phenotypic Variability and Challenges in Risk Stratification. [PDF]

open access: yesJ Clin Med
Bouzón P   +10 more
europepmc   +1 more source

Atypical Andersen-Tawil Syndrome in an Asymptomatic Child With Bidirectional Ventricular Tachycardia and Incipient Tachycardiomyopathy. [PDF]

open access: yesJACC Case Rep
Assunção MELSM   +5 more
europepmc   +1 more source

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