Publications by authors named "R E McClellan"

The electromagnetic form factors of the proton and neutron encode information on the spatial structure of their charge and magnetization distributions. While measurements of the proton are relatively straightforward, the lack of a free neutron target makes measurements of the neutron's electromagnetic structure more challenging and more sensitive to experimental or model-dependent uncertainties. Various experiments have attempted to extract the neutron form factors from scattering from the neutron in deuterium, with different techniques providing different, and sometimes large, systematic uncertainties.

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Study Design: Prospective cross-sectional survey.

Objective: To identify timelines for when athletes may be considered safe to return to varying athletic activities after sustaining cervical spine fractures.

Background: While acute management and detection of cervical spine fractures have been areas of comprehensive investigation, insight into timelines for when athletes may return to different athletic activities after sustaining such fractures is limited.

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Background: The mechanisms of AF development and progression are still not completely understood. Despite the relative efficacy of ablation, the risk of AF recurrence is substantial, particularly in patients with persistent AF (perAF). At present we do not have any reliable intra-procedural electrophysiologic predictors of long-term success of AF ablation other than pulmonary vein isolation.

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Article Synopsis
  • Genetic testing is essential for diagnosing long QT syndrome (LQTS) and can provide valuable information for patients and their families, but about 25% of patients show no identifiable genetic variants despite having significant symptoms.
  • The prognosis for these patients mirrors that of those with known genetic variants, highlighting the need to investigate various potential causes of QT interval prolongation beyond genetic factors, including environmental influences and exercise-related issues.
  • Continuous advancements in genetics may reveal new risk factors and causal genes for LQTS, emphasizing the importance of expert cardiogenetic clinics in effectively managing and counseling affected patients, especially those with unclear genetic test results.
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