Collaboration agreement between Telethon Foundation and Rare Partners

Telethon has renewed the agreement with Rare Partners for the development of diagnostic tools and therapeutic approaches based on the results of research projects funded by the Telethon Foundation.

From Research


Possible culprits in congenital heart defects identified

Researchers at Washington University School of Medicine in St. Louis and the University of Padua-Dulbecco Telethon Institute in Italy have shown that mitochondria remarkably also orchestrate events that determine a cell's future, at least in the embryonic mouse heart

From Research


New "muscle-saver" molecular strategy discovered

A new molecular strategy is described for enhancement of muscle growth and for consequent containment of the adverse effects of degenerative diseases such as muscular dystrophy and atrophy

From Research


Research: correlation discovered between neurological deficits and ferritin deficiency

A study conducted by researchers at IRCCS Ospedale San Raffaele Milano, funded by Telethon and coordinated by Prof. Sonia Levi was published in The Journal of Experimental Medicine.

From Research


Mitochondrial diseases: here's the metabolism-helper gene

A case of malfunctioning mitochondria? Considerable help may be provided by OPA1 – a gene which, when altered, is known to be responsible for a hereditary disease of the eye, dominant optic atrophy.

From Research


The Hiv virus used to cure two severe genetic diseases

The AIDS virus can be used to treat two severe hereditary diseases.

From Research


The Dulbecco Telethon Institute International Postdoctoral Programme: DTI-IMPORT, 10 January first call open!

DTI-IMPORT (co-funded by the European Community within the Marie Curie Actions of the 7FWP) is intended to provide an excellent training to experienced researchers and, at the same time, enhance the internationalization in the Dulbecco Telethon Institute (DTI).

From Research


Alliance between Fondazione Telethon and biopharmaceutical company Shire for research and development of new therapies for rare genetic diseases

Fondazione Telethon has signed an important agreement to collaborate with the international pharma company Shire plc.

From Research


Molecular bullets on the way for cystic fibrosis, Sma and haemophilia

Researchers at the ICGEB in Trieste and at Ferrara University have created a therapeutic strategy based on small RNAs in order to bypass the genetic defect responsible for these serious diseases still without a permanent cure.

From Research

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