Membrane physiology and biophysics—Another milestone
Christoph Fahlke
doaj +1 more source
The Short QT Syndrome is a recently described new genetic disorder, characterized by abnormally short QT interval, paroxysmal atrial fibrillation and life threatening ventricular arrhythmias. This autosomal dominant syndrome can afflict infants, children,
Lia Crotti +3 more
doaj
Correction: Impact of social factors and health campaigns on the burden of idiopathic epilepsy: an inequality, decomposition, generalized and synthetic difference-in-differences study. [PDF]
Rong X +7 more
europepmc +1 more source
Editorial: Emerging perspectives in sodium channelopathies
J. R. Groome +3 more
doaj +1 more source
Hidden Cardiac Channelopathies in Children Presenting with Syncope and Seizure-like Events. [PDF]
Aytekin Güvenir F, Özgür S.
europepmc +1 more source
Estimation of Incidence and Prevalence of Pediatric Channelopathies in a Mediterranean Population Based on a Single-Center, Retrospective Analysis. [PDF]
Bagkaki A +6 more
europepmc +1 more source
Cardiac channelopathies in the context of hereditary arrhythmia syndromes
Hereditäre Arrhythmiesyndrome sind seltene Erkrankungen, die allerdings im Kindes‑, Jugend- und jungen Erwachsenenalter eine häufige Ursache des plötzlichen Herztods darstellen.
Huttelmaier, Moritz T. +1 more
core +1 more source
SCN4A Channelopathies: From Disease Mechanisms to Variant Interpretation. [PDF]
D'Ambrosio P +7 more
europepmc +1 more source
Electrocardiographic Dynamism in Arrhythmia Practice: From Channelopathies to Drug Toxicity. [PDF]
Özalp TA.
europepmc +1 more source

