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Showing 1827 results
February 2014
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Parenting a child with a rare disease
Raising a child with a rare disease can feel overwhelming and isolating, but many parents end up being extremely proud of their children’s achievements.
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Creative ways to help kids understand rare diseases
Parents and doctors can help children understand rare diseases like TSC and SJIA with the help of cartoon dogs and comic book superheroes.
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Text messages in Africa help to fight malaria
After 40 years of working in information technology, Jim Barrington took a partial retirement from his job as Novartis’ chief information officer and started looking for new ways to apply his skills.
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Talking to: Ann Aerts, Head of the Novartis Foundation
With extensive experience in public health management, having worked for the International Red Cross, among others, and as a doctor in emergency situations on the ground in Africa and Asia— Ann Aerts discusses the Novartis Foundation's new leprosy strategy.
November 2013
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Telemedicine: Taking health care to the world's far corners
Ann Aerts has stared death in the eye. The head of the non-profit Novartis Foundation lost colleagues when she was serving as an emergency medicine physician on a medical mission in a dangerously unstable country.
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Fighting malaria in Africa
The head of Public Affairs for the Novartis Malaria Initiative has a malaria story of her own to tell.
October 2013
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Young talent & emerging technologies come together at BioCamp
University students majoring in the life sciences or business often have trouble imagining the direction of their careers.
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Protecting our tomorrows: Portraits of Meningococcal Disease
To raise awareness of the sudden and profound impact of meningococcal disease on families across the globe, world-renowned photographer Anne Geddes has joined forces with the Confederation of Meningitis Organizations (CoMO) and Novartis Vaccines and Diagnostics for the Protecting Our Tomorrows: Portraits of Meningococcal Disease project.
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Disease pathways: A key to new drug discovery
Using new technologies, researchers have developed a deeper understanding of how cells function, changing conceptions of disease.
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Tackling a rare disease: Working toward a treatment for SMA
Most people have never heard of spinal muscular atrophy (SMA), a rare genetic disease that affects approximately 1 in 6,000 babies born worldwide each year. Innovative research may produce treatments for patients suffering from SMA and other rare diseases.
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