minority diseases

Cellers Maset creates the Pau Massana Scholarship for the research of minority diseases of the I3PT
Cellers Maset creates the Pau Massana Scholarship for the research of minority diseases of the I3PT 1080 608 Mireia Córcoles

The entity has signed a collaboration agreement with the Parc Taulí Research and Innovation Institute to raise funds through a solidarity wine initiative, and to contribute €25.000 annually for research into minority diseases Cellers Maset and the Parc Taulí Research and Innovation Institute (I3PT) have signed a collaboration agreement for the creation of the first Pau Massana Scholarship for Rare Diseases. This scholarship is an initiative of the winery for…

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Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome
Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome 1080 675 Guillem Cebrian

Prader-Willi syndrome (PWS) is a disease of uncommon genetic origin considered, however, the most common cause of genetic obesity. According to data extracted from the web portal of the Spanish SPW Association, this disease affects one in 15.000 newborns. A scientific article on this disease was recently published in The Journal of Clinical Endocrinology & Metabolism with the participation of several international researchers who are experts in this syndrome. Among them is Dr.…

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