A group of Japanese scientists from the University of Tokyo managed to visually capture the aura of a person, thus proving its existence!
With the assistance of highly sensitive cameras the scientists were able to photograph a person’s special glow.
Notably, the glow appears brightest in the morning and seems to “fade” in the evening. It is most visible around the face, mouth, cheeks and neck.
Experts believe that this technique could become a new tool for use in the diagnosis and treatment of many diseases. A faint glow around certain body parts may indicate the presence of a disease or disorder.
La majorité des français semble prête à faire confiance aux outils numériques connectés pour la gestion partagée de leurs données de santé, ainsi que pour leur participation active au fonctionnement de leur DMP.
3-D printing used to construct everything from art to toys to spare parts for the space station may one day produce human organs at a hospital near you.
The 20-year-old technology uses liquid materials that become hard as they print out three-dimensional objects in layers, based on a digital model. Current medical uses are in dentistry, for hard-material crowns, caps and bridges, as well as prosthetics. Last year, a 3-D printer was used to create a structure from moldable polymer that replaced more than 75 percent of a patient’s skull.
Now, Organovo Holdings Inc. is using 3-D printers to create living tissue that may one day look and act like a human liver, able to cleanse the body of toxins. Drugmakers and cosmetic companies already plan to use 3-D printed human tissue to test new products. Eventually, the technology may help reduce organ shortages and cut transplant rejections as patients receive new organs constructed from their own cells.
La France est en retard sur l'open data en matière de santé. L'explication tient au conservatisme des professions médicales et de l'assurance maladie malgré l'intérêt économique et sanitaire non négligeable de la question.
Face aux demandes répétées des investisseurs et entrepreneurs, la FDA définit les catégories d’applications concernées par son autorité sans pour autant clarifier la mise en application de ses recommandations.
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