A small team of physical education scientists in China has conducted a meta-analysis of multiple studies that shows that dancing is an effective weight loss intervention. In their study, reported in the open-access journal ...
University of Alberta researchers have identified a neurochemical marker related to the loss of motor function and communication breakdown between the primary motor cortex—the part of the brain that controls our muscles—and ...
May 4, 2023
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A gene variant that affects skeletal muscle function may have protected humans against lower temperatures as they migrated from Africa to Europe more than 50,000 years ago, suggests a study appearing February 17 in the American ...
Feb 17, 2021
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When we dream, our brains are filled with noisy electrical activity that looks nearly identical to that of the awake brain.
Aug 7, 2020
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At 19 months old, Elijah Jack, born with no femur bone in one leg and a short femur in the other, is unable to walk on his own like most toddlers his age. Another 19-month-old, Freya Baudoin, born prematurely at 28 weeks ...
Dec 21, 2023
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Jeffrey Raskin, MS, MD, a neurosurgeon at Ann & Robert H. Lurie Children's Hospital of Chicago, performed the first ever computer-guided radiofrequency ablation to decrease excessive muscle tone (called hypertonia) in a child ...
Sep 21, 2023
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Researchers at Ruhr University Bochum, Germany, have successfully implemented a special form of classical conditioning. They showed on a group of 75 people that effects of transcranial magnetic stimulation (TMS) can be triggered ...
Apr 24, 2023
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An experimental wrist-worn device was found to predict troponin-I and obstructed arteries with 90% accuracy in five minutes, according to research presented at the American College of Cardiology's Annual Scientific Session ...
Mar 7, 2023
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Brief resolved unexplained events (BRUEs) are episodes marked by concerning changes in breathing, consciousness, muscle tone, and skin color (cyanosis or paleness). They tend to occur in previously healthy infants and send ...
Jan 4, 2023
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Glutaric aciduria type I (GA-I) is an inherited disease caused by a mutation of the glutaryl-CoA dehydrogenase (GCDH) gene. The global incidence of GA-I is estimated to be 1/100,000, with around 75,000 cases worldwide.
Nov 29, 2022
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