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Towards Clinical Molecular Diagnosis of Inherited Cardiac Conditions: A Comparison of Bench-Top Genome DNA Sequencers
TLDR
MiSeq and Ion Torrent PGM both provide accurate variant detection as part of a PCR-based molecular diagnostic workflow, and provide alternative platforms for molecular diagnosis of inherited cardiac conditions.
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Subject-specific profiles of QT/RR hysteresis.
TLDR
The speed with which the QT interval adapts to heart rate changes is highly individual with intrasubject stability and intersubject variability, which is likely to lead to substantial improvements of cardiac repolarization studies.
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Right ventricular myocardial infarction: From pathophysiology to prognosis.
TLDR
Right ventricular involvement appears to be an independent prognostic factor that dramatically increases in-hospital mortality, due, in part, to a significantly higher risk of hemodynamically compromising arrhythmias.
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Pseudoaneurysm of the Dorsalis Pedis Artery: Case Report and Literature Review.
TLDR
The case of a 57-year-old male with an idiopathic pseudoaneurysm of the dorsalis pedis artery, a rare vascular entity usually caused by traumatic injury or iatrogenic intervention, which recovered well after surgery and remained free of symptoms 18 months postoperatively is reported.
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The learning curve of robot-assisted laparoscopic aortofemoral bypass grafting for aortoiliac occlusive disease.
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Data analysis of diagnostic accuracies in 12-lead electrocardiogram interpretation by junior medical fellows.
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The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano–Ward Syndrome
TLDR
The clinical relevance of these findings is that apparently normal individuals may have a latent reduction of repolarizing currents, a “reduced repolarization reserve,” because they are carriers of latent ion channel genes mutations.
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Dynamic properties of selected repolarization descriptors.
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Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease
TLDR
Test the hypothesis that ion channel genes mutations are more common in ventricular fibrillation survivors with coronary artery disease compared to controls to demonstrate a strong genetic component of sudden cardiac death.
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Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome.
TLDR
A hypothesis that other candidate genes could be involved in LQTS pathophysiology is tested by screening coding regions of genes SCN1B, KCND3, and 10 exons of ANK2 and finding five polymorphisms found in screened candidate genes.
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