Tag: minority diseases I3PT Parc Taulí

A cystic fibrosis project of the I3PT, winner of the Pau Massana Grant

A cystic fibrosis project of the I3PT, winner of the Pau Massana Grant https://www.tauli.cat/institut/wp-content/uploads/2023/04/beca-pau-massana-i3pt-1200x675.jpg 1080 608 Mireia Córcoles Mireia Córcoles https://www.tauli.cat/institut/wp-content/uploads/2022/11/Tezza-0184-150x150.jpg April 26, 2023 May 31, 2023

By: Mireia Córcoles

April 26, 2023

The Cellers Maset scholarship is endowed with €25.000, and will allow funding each year for a research project on minority diseases read more

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 https://www.tauli.cat/institut/wp-content/uploads/2022/11/Plantilla-Imatges-169-Web-1200x675.png 1080 608 Mireia Córcoles Mireia Córcoles https://www.tauli.cat/institut/wp-content/uploads/2022/11/Tezza-0184-150x150.jpg November 18, 2022 November 18, 2022

By: Mireia Córcoles

November 18, 2022

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…

Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome

Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome https://www.tauli.cat/institut/wp-content/uploads/2020/04/8559-min-min_opt-1200x750.jpg 1080 675 Guillem Cebrian Guillem Cebrian https://www.tauli.cat/institut/wp-content/uploads/2020/02/IMG-1030-150x150.png April 16, 2020 March 25, 2021

By: Guillem Cebrian

April 16, 2020

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.…