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Michael H. Smolensky

Researcher at University of Texas at Austin

Publications -  134
Citations -  6076

Michael H. Smolensky is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Ambulatory blood pressure & Blood pressure. The author has an hindex of 37, co-authored 127 publications receiving 5389 citations. Previous affiliations of Michael H. Smolensky include University of Vigo & University of Texas Health Science Center at Houston.

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Ethics and methods for biological rhythm research on animals and human beings

TL;DR: The ethical standards and methods for the conduct of high-quality animal and human biological rhythm research are updated, which should be especially useful for new investigators of the rhythms of life.
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Shift work and cancer risk: potential mechanistic roles of circadian disruption, light at night, and sleep deprivation.

TL;DR: The possible multiple and interconnected cancer-promoting mechanisms as a consequence of shift work are examined, i.e., repeated disruption of the circadian system, pineal hormone melatonin suppression by exposure to light at night, sleep-deprivation-caused impairment of the immune system, plus metabolic changes favoring obesity and generation of proinflammatory reactive oxygen species.
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Circadian rhythms and cardiovascular health.

TL;DR: Knowing of 24-h patterns in the risk of cardiac arrhythmias and cardiovascular disease morbidity and mortality plus circadian rhythm-dependencies of underlying pathophysiologic mechanisms suggests the requirement for preventive and therapeutic interventions is not the same throughout the day and night, and should be tailored accordingly to improve outcomes.
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2013 Ambulatory Blood Pressure Monitoring Recommendations for the Diagnosis of Adult Hypertension, Assessment of Cardiovascular and other Hypertension-associated Risk, and Attainment of Therapeutic Goals

TL;DR: ABPM should be viewed as the new gold standard to diagnose true hypertension, accurately assess consequent tissue/organ, maternal/fetal, and CVD risk, and individualize hypertension chronotherapy.