Clínic Barcelona
Clínic Barcelona
January 30 2012
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Clínic Barcelona
Clínic Barcelona
January 26 2012
The last IDIBAPS seminar focused on the advancement in cirrhosis classification
The diagnosis of cirrhosis has experienced important progresses in recent years. In addition to improved techniques for a good diagnose, this diag1
Clínic Barcelona
Clínic Barcelona
January 26 2012
A multimedia application for schools to learn about biomedicine and how does a laboratory work
Multimedia applications are an ideal tool to stimulate learning and explaining complex concepts. That is the reason Institut d’Investigacions Biomèdi1
Clínic Barcelona
Clínic Barcelona
January 24 2012
The meetinc Challenges and risks of Research on Advanced Therapies brings together more than a hundred scientists, companies and professionals
Clínic Barcelona
Clínic Barcelona
January 24 2012
Histocell will develop a cell therapy against lung fibrosis based on a patent from the CSIC and the Hospital Clínic
Histocell, Hospital Clínic de Barcelona and the Higher Council for Scientific Research (CSIC) have signed a licensing agreement
Clínic Barcelona
Clínic Barcelona
January 20 2012
Can dogs detect hypoglycaemia and assist a patient during one of these episodes?
Dogs often show an altered behaviour when a crisis of hypoglycaemia is about to occur to one of his owners
Clínic Barcelona
Clínic Barcelona
January 18 2012
IDIBAPS joins an ambitious project to find a cure for Huntington's disease
By now Huntington\'s disease has no effective treatment, and there are no appropriate experimental models to study potential drugs. The Cure of Hunti1
Clínic Barcelona
Clínic Barcelona
January 16 2012
The AIDS research team launches a new website
Some IDIBAPS´ research teams have specific online needs. A recent example is the AIDS research team, led by Dr. Josep Maria Gatell, which introduces1
Clínic Barcelona
Clínic Barcelona
January 9 2012
New gene identified whose mutations cause a fatal mitochondrial encephalopathy
An article in the American Journal of Human Genetics identifies a new gene whose mutations cause a fatal childhood disease with encephalopathy and pu1