Results 61 to 70 of about 182,456 (375)

Sources of Measurement Error in an ECG Examination: Implications for Performance-Based Assessments [PDF]

open access: yes, 2004
Objective: To assess the sources of measurement error in an electrocardiogram (ECG) interpretation examination given in a third-year internal medicine clerkship. Design: Three successive generalizability studies were conducted.
Frerenchick, Gary, Solomon, David J
core   +1 more source

Potentiating Cerebral Perfusion Normalizes Glymphatic Dynamics in Systemic Inflammation

open access: yesAdvanced Science, EarlyView.
LPS‐induced systemic inflammation increases glymphatic influx but delays cervical lymphatic drainage, accompanied by AQP4 depolarization and impaired glymphatic clearance. Enhancing cerebral blood flow via the inotropic agent levosimendan effectively restored AQP4 polarization, improving glymphatic flux and amyloid‐β clearance.
Ruoyu Zhao   +9 more
wiley   +1 more source

Analysis of the success rate of conversion using ibutilide administration in radiofrequency catheter ablation of persistent atrial fibrillation and its effects on postoperative recurrence

open access: yesBMC Cardiovascular Disorders
Objective To assess the efficacy of ibutilide administration during radiofrequency catheter ablation of persistent atrial fibrillation (AF), to explore the success rate of conversion and related influential factors, and to analyze the effects of ...
Meijuan Li   +6 more
doaj   +1 more source

Assessing Cardiac Sympatho-Vagal Balance Through Wavelet Transform Analysis of Heart Rate Variability

open access: yesApplied Sciences
Heart rate variability (HRV), which is the variation between consecutive heartbeats, reflects the electrical activity of the heart and provides insight into the autonomic nervous system (ANS) function.
A.M. Nelushi   +3 more
doaj   +1 more source

Decreased RYR2 Cluster Size and Abnormal SR Ca2+ Release Contribute to Arrhythmogenesis in TMEM43‐Related ARVC

open access: yesAdvanced Science, EarlyView.
The TMEM43 ‐ P386S mutation causes arrhythmogenic right ventricular cardiomyopathy (ARVC) by mislocalizing itself from nuclear envelope (NE) to cytoplasm, disrupting lamin B2 (a novel TMEM43 interactor) localization, NE integrity and chromatin accessibility, causing hyper ‐ phosphorylation and reduced expression/clustering of ryanodine receptor type 2 (
Jiaxi Shen   +23 more
wiley   +1 more source

Acupuncture Treatment of a Patient with Bradycardia and Idioventricular Rhythm

open access: yesJournal of Acupuncture & Meridian Studies, 2022
A patient with bradycardia and an idioventricular rhythm was observed. According to cardiologists, there is no reliable drug treatment for bradycardia with an idioventricular rhythm; instead, the sole treatment is a pacemaker. In the course of this case,
Oksana Strakhova, Alexey Ryzhov
doaj   +1 more source

Electrocardiography in horses, part 2: how to read the equine ECG [PDF]

open access: yes, 2010
The equine practitioner is faced with a wide variety of dysrhythmias, of which some are physiological. The recording of an exercise electrocardiogram (ECG) can help distinguish between physiological and pathological dysrhythmias, underlining the ...
De Clercq, Dominique   +5 more
core  

Advances in Organic In‐Sensor Neuromorphic Computing: from Material Mechanisms to Applications

open access: yesAdvanced Intelligent Discovery, EarlyView.
This review discusses organic in‐sensor neuromorphic computing for wearable and bioelectronic systems, with a focus on memory‐based and OECT‐based synaptic devices. It highlights key design principles, recent advances, and existing challenges. By integrating sensing and processing within organic materials, the approach enables real‐time, low‐power, and
Dong Hyun Lee   +3 more
wiley   +1 more source

Resistance to thyroid hormone accompanied by atrial fibrillation

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2018
Resistance to thyroid hormone (RTH), which is primarily caused by mutations in the thyroid hormone (TH) receptor beta (THRB) gene, is dominantly inherited syndrome of variable tissue hyposensitivity to TH.
Haruhiro Sato, Yuichiro Tomita
doaj   +1 more source

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil   +8 more
wiley   +1 more source

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