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minority diseases

A project for research into Prader-Willi syndrome, winner of the Pau Massana Grant
 A project for research into Prader-Willi syndrome, winner of the Pau Massana Grant 1080 608 Oriol Capell
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For three editions, the I3PT has collaborated with Cellers Maset for the research and development of projects that improve the quality of life of people with rare diseases. read more
A project for the research of Angelman syndrome, winner of the Pau Massana Grant
 A project for the research of Angelman syndrome, winner of the Pau Massana Grant 1080 608 Oriol Capell
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The study, led by researchers Marta Moraleda and Débora Itzep, will investigate the sleep and circadian rhythm disorders of children and adolescents with this pathology read more
Investigating Fragile X syndrome in girls and adolescents
 Investigating Fragile X syndrome in girls and adolescents 1080 608 Oriol Capell
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As part of World Minority Disease Day, we are publishing the second installment of the 'Presenta la teva tesi' series. Lorena Joga, child and youth neuropsychologist at Parc Taulí and researcher at the I3PT explains what Fragile X Syndrome is and how it affects girls and teenagers. read more
I3PT, CONNECTA Therapeutics, CRG and IMIM receive 2,7 million from the Ministry of Science and Innovation to start Phase IIa of the drug CTH120 for fragile X syndrome
 I3PT, CONNECTA Therapeutics, CRG and IMIM receive 2,7 million from the Ministry of Science and Innovation to start Phase IIa of the drug CTH120 for fragile X syndrome 1080 608 Mireia Córcoles
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The Phase IIa study will evaluate the efficacy of CTH120 as an innovative therapy in adult patients with FXS, the most common form of inherited intellectual disability without a specific treatment read more
The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros
 The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros 1080 608 Oriol Capell
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The endowment will serve to finance the clinical trial of an innovative therapy for patients with Fragile X Syndrome and the discovery and clinical development of new PDE-10 inhibitors for the treatment of Prader-Willi syndrome read more
Parc Taulí organizes the first European Workshop on Angelman Syndrome in Catalonia
 Parc Taulí organizes the first European Workshop on Angelman Syndrome in Catalonia 1080 608 Mireia Córcoles
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The aim of the first edition of the EWAS was to improve the clinical approach and research of this minority disease read more
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