Call for admission - Food, Nutrition and Health - EU or EU-equated citizens - (int. 2026-27) -

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“I LUOGHI DI PROVA DEL DIPARTIMENTO ICEA”. Esposizione fotografica dal 20 dicembre 2025 al 15 gennaio 2026

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Bando di ammissione - Food, Nutrition and Health - EU or EU-equated citizens - (int. 2026-27) -

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Call for admission - AnimalCare - EU or EU-equated citizens - (int. 2026-27) -

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Bando di ammissione - AnimalCare - EU or EU-equated citizens - (int. 2026-27) -

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Seduta del 4 novembre 2025

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Erdera selects two projects from the University of Padua

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

[summary] => [format] => 2 [safe_value] =>

Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

[summary] => [format] => 2 [safe_value] =>

Two projects from the University of Padua have been selected as part of the transnational Erdera (European Rare Diseases Research Alliance) call for proposals and funded by the Telethon Foundation. These include Tania Zaglia's study on arrhythmogenic cardiomyopathy and Stefano Comai's research on Fragile X syndrome and Phelan-McDermid syndrome.

The TREATYNG project, coordinated by Tania Zaglia (Department of Biomedical Sciences), investigates arrhythmogenic cardiomyopathy as a multicellular disease and evaluates neuropeptide-Y as a potential therapeutic target to slow disease progression, also developing new prognostic biomarkers.

The MT2ASD project, led by Stefano Comai (Department of Pharmaceutical Sciences), focuses on evaluating selective agonist drugs for the MT2 melatonin receptor as a new therapeutic approach for Fragile X syndrome and Phelan-McDermid syndrome, with the aim of preparing future clinical studies.

The projects selected by Erdera cover numerous rare and severe diseases and aim to produce solid preclinical evidence for the development of safer and more effective therapies. In the 2025 edition of the call, 18 transnational projects were funded out of 161 initial proposals, with a total budget of approximately 29 million euros, supported by 29 funding bodies from 23 countries and co-financed by the European Commission.

For Italy, participants included, among others, the Telethon Foundation, the Ministry of Health, and the Ministry of University and Research.

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CONSEGNATI OGGI I PREMI DI STUDIO GIULIA CECCHETTIN

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Erdera seleziona due progetti dell’Università di Padova

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Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

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Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

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Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

[summary] => [format] => 2 [safe_value] =>

Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

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Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

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Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

[summary] => [format] => 2 [safe_value] =>

Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

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Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

[summary] => [format] => 2 [safe_value] =>

Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

[safe_summary] => ) ) ) [field_date_box_lancio_news] => Array ( [und] => Array ( [0] => Array ( [value] => 2025-12-18T00:00:00 [timezone] => Europe/Paris [timezone_db] => Europe/Paris [date_type] => date ) ) ) [field_etichetta_box_lancio_news] => Array ( ) [field_img_box_lancio_news] => Array ( [und] => Array ( [0] => Array ( [fid] => 144885 [uid] => 26499 [filename] => n_microscopio_0.jpg [uri] => public://n_microscopio_0_0.jpg [filemime] => image/jpeg [filesize] => 43729 [status] => 1 [timestamp] => 1766066462 [type] => image [field_file_image_alt_text] => Array ( ) [field_file_image_title_text] => Array ( ) [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2048 ) ) ) [metadata] => Array ( [height] => 302 [width] => 677 ) [height] => 302 [width] => 677 [alt] => microscopio [title] => ) ) ) [field_link_alla_news] => Array ( ) [field_link_esterno_news] => Array ( ) [field_pagina_associata] => Array ( ) [field_link_etichetta] => Array ( ) [field_abstract_news] => Array ( [und] => Array ( [0] => Array ( [value] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid [format] => [safe_value] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid ) ) ) [field_allegato_news] => Array ( ) [field_categorie_news] => Array ( [und] => Array ( [0] => Array ( [tid] => 2264 ) [1] => Array ( [tid] => 2266 ) [2] => Array ( [tid] => 2267 ) [3] => Array ( [tid] => 2462 ) ) ) [field_pub_date] => Array ( [und] => Array ( [0] => Array ( [value] => 2025-12-18T00:00:00 [value2] => 2026-12-18T00:00:00 [timezone] => Europe/Paris [timezone_db] => Europe/Paris [date_type] => date ) ) ) [field_layout_news] => Array ( [und] => Array ( [0] => Array ( [value] => single ) ) ) [field_testo_opzionale_news] => Array ( ) [field_url_en_page] => Array ( [und] => Array ( [0] => Array ( [value] => https://www.unipd.it/news/erdera-selects-two-projects-university-padua [format] => [safe_value] => https://www.unipd.it/news/erdera-selects-two-projects-university-padua ) ) ) [field_url_en_page_label] => Array ( [und] => Array ( [0] => Array ( [value] => English version [format] => [safe_value] => English version ) ) ) [path] => Array ( [pathauto] => 1 ) [name] => rossella.vezzosi [picture] => 0 [data] => b:0; [num_revisions] => 2 [current_revision_id] => 513756 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) [#items] => Array ( [0] => Array ( [value] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid [format] => [safe_value] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid ) ) [#formatter] => text_default [0] => Array ( [#markup] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid ) ) [links] => Array ( [#theme] => links__node [#pre_render] => Array ( [0] => drupal_pre_render_links ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) [node] => Array ( [#theme] => links__node__node [#links] => Array ( [node-readmore] => Array ( [title] => Read more about Erdera seleziona due progetti dell’Università di Padova [href] => node/126510 [html] => 1 [attributes] => Array ( [rel] => tag [title] => Erdera seleziona due progetti dell’Università di Padova ) ) ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) ) ) [field_date_box_lancio_news] => Array ( [#theme] => field [#weight] => 1 [#title] => Data [#access] => 1 [#label_display] => above [#view_mode] => teaser [#language] => und [#field_name] => field_date_box_lancio_news [#field_type] => date [#field_translatable] => 0 [#entity_type] => node [#bundle] => box_lancio_news [#object] => stdClass Object ( [vid] => 513756 [uid] => 26499 [title] => Erdera seleziona due progetti dell’Università di Padova [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 126510 [type] => box_lancio_news [language] => it [created] => 1766066462 [changed] => 1766067085 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1766067085 [revision_uid] => 26499 [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

[summary] => [format] => 2 [safe_value] =>

Due progetti dell'Università di Padova sono stati selezionati nell'ambito del bando transnazionale Erdera (European Rare Diseases Research Alliance) e finanziati dalla Fondazione Telethon. Si tratta dello studio di Tania Zaglia sulla cardiomiopatia aritmogena e di quello di Stefano Comai sulla sindrome del cromosoma X fragile e la sindrome di Phelan-McDermid.

Il progetto TREATYNG, coordinato da Tania Zaglia (Dipartimento di Scienze biomediche), indaga la cardiomiopatia aritmogena come patologia multicellulare e valuta il neuropeptide-Y come possibile bersaglio terapeutico per rallentare la progressione della malattia, sviluppando anche nuovi biomarcatori prognostici.

Il progetto MT2ASD, guidato da Stefano Comai (Dipartimento di Scienze del farmaco), è invece dedicato alla valutazione di farmaci agonisti selettivi del recettore MT2 della melatonina come nuovo approccio terapeutico per la sindrome dell'X fragile e la sindrome di Phelan-McDermid, con l'obiettivo di preparare futuri studi clinici.

I progetti selezionati da Erdera coprono numerose malattie rare e gravi e mirano a produrre solide evidenze precliniche per lo sviluppo di terapie più sicure ed efficaci. Nell'edizione 2025 del bando sono stati finanziati 18 progetti transnazionali su 161 proposte iniziali, per un budget complessivo di circa 29 milioni di euro, con il sostegno di 29 enti finanziatori di 23 Paesi e il co-finanziamento della Commissione europea.

Per l'Italia hanno partecipato, tra gli altri, la Fondazione Telethon, il Ministero della Salute e il Ministero dell'Università e della Ricerca.

[safe_summary] => ) ) ) [field_date_box_lancio_news] => Array ( [und] => Array ( [0] => Array ( [value] => 2025-12-18T00:00:00 [timezone] => Europe/Paris [timezone_db] => Europe/Paris [date_type] => date ) ) ) [field_etichetta_box_lancio_news] => Array ( ) [field_img_box_lancio_news] => Array ( [und] => Array ( [0] => Array ( [fid] => 144885 [uid] => 26499 [filename] => n_microscopio_0.jpg [uri] => public://n_microscopio_0_0.jpg [filemime] => image/jpeg [filesize] => 43729 [status] => 1 [timestamp] => 1766066462 [type] => image [field_file_image_alt_text] => Array ( ) [field_file_image_title_text] => Array ( ) [field_folder] => Array ( [und] => Array ( [0] => Array ( [tid] => 2048 ) ) ) [metadata] => Array ( [height] => 302 [width] => 677 ) [height] => 302 [width] => 677 [alt] => microscopio [title] => ) ) ) [field_link_alla_news] => Array ( ) [field_link_esterno_news] => Array ( ) [field_pagina_associata] => Array ( ) [field_link_etichetta] => Array ( ) [field_abstract_news] => Array ( [und] => Array ( [0] => Array ( [value] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid [format] => [safe_value] => Finanziati da Fondazione Telethon gli studi di Tania Zaglia sulla cardiomiopatia aritmogena e quelli di Stefano Comai sulla sindrome del cromosoma X fragile e sindrome di Phelan McDermid ) ) ) [field_allegato_news] => Array ( ) [field_categorie_news] => Array ( [und] => Array ( [0] => Array ( [tid] => 2264 ) [1] => Array ( [tid] => 2266 ) [2] => Array ( [tid] => 2267 ) [3] => Array ( [tid] => 2462 ) ) ) [field_pub_date] => Array ( [und] => Array ( [0] => Array ( [value] => 2025-12-18T00:00:00 [value2] => 2026-12-18T00:00:00 [timezone] => Europe/Paris [timezone_db] => Europe/Paris [date_type] => date ) ) ) [field_layout_news] => Array ( [und] => Array ( [0] => Array ( [value] => single ) ) ) [field_testo_opzionale_news] => Array ( ) [field_url_en_page] => Array ( [und] => Array ( [0] => Array ( [value] => https://www.unipd.it/news/erdera-selects-two-projects-university-padua [format] => [safe_value] => https://www.unipd.it/news/erdera-selects-two-projects-university-padua ) ) ) [field_url_en_page_label] => Array ( [und] => Array ( [0] => Array ( [value] => English version [format] => [safe_value] => English version ) ) ) [path] => Array ( [pathauto] => 1 ) [name] => rossella.vezzosi [picture] => 0 [data] => b:0; [num_revisions] => 2 [current_revision_id] => 513756 [is_current] => 1 [is_pending] => [revision_moderation] => [entity_view_prepared] => 1 ) [#items] => Array ( [0] => Array ( [value] => 2025-12-18T00:00:00 [timezone] => Europe/Paris [timezone_db] => Europe/Paris [date_type] => date ) ) [#formatter] => date_default [0] => Array ( [#markup] => Gio, 18/12/2025 ) ) )

Documenti - selezione 2025N64

Array ( [body] => Array ( [#theme] => field [#weight] => 0 [#title] => Body [#access] => 1 [#label_display] => hidden [#view_mode] => teaser [#language] => und [#field_name] => body [#field_type] => text_with_summary [#field_translatable] => 0 [#entity_type] => node [#bundle] => tab [#object] => stdClass Object ( [vid] => 513750 [uid] => 29556 [title] => Documenti - selezione 2025N64 [log] => [status] => 1 [comment] => 0 [promote] => 1 [sticky] => 0 [nid] => 126509 [type] => tab [language] => it [created] => 1766065814 [changed] => 1768552969 [tnid] => 0 [translate] => 0 [revision_timestamp] => 1768552969 [revision_uid] => 32 [body] => Array ( [und] => Array ( [0] => Array ( [value] =>

Per partecipare alla selezione è necessario compilare e presentare la domanda attraverso la procedura online.

Leggere attentamente le istruzioni.

Procedura telematica di compilazione e presentazione della domanda 

La procedura di compilazione e l’invio telematico della domanda dovranno essere completati entro la data di scadenza del Bando.

[summary] => [format] => 2 [safe_value] =>

Per partecipare alla selezione è necessario compilare e presentare la domanda attraverso la procedura online.

Leggere attentamente le istruzioni.

Procedura telematica di compilazione e presentazione della domanda 

La procedura di compilazione e l’invio telematico della domanda dovranno essere completati entro la data di scadenza del Bando.

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Per partecipare alla selezione è necessario compilare e presentare la domanda attraverso la procedura online.

Leggere attentamente le istruzioni.

Procedura telematica di compilazione e presentazione della domanda 

La procedura di compilazione e l’invio telematico della domanda dovranno essere completati entro la data di scadenza del Bando.

[summary] => [format] => 2 [safe_value] =>

Per partecipare alla selezione è necessario compilare e presentare la domanda attraverso la procedura online.

Leggere attentamente le istruzioni.

Procedura telematica di compilazione e presentazione della domanda 

La procedura di compilazione e l’invio telematico della domanda dovranno essere completati entro la data di scadenza del Bando.

[safe_summary] => ) ) [#formatter] => text_summary_or_trimmed [0] => Array ( [#markup] =>

Per partecipare alla selezione è necessario compilare e presentare la domanda attraverso la procedura online.

Leggere attentamente le istruzioni.

Procedura telematica di compilazione e presentazione della domanda 

La procedura di compilazione e l’invio telematico della domanda dovranno essere completati entro la data di scadenza del Bando.

) ) [links] => Array ( [#theme] => links__node [#pre_render] => Array ( [0] => drupal_pre_render_links ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) [node] => Array ( [#theme] => links__node__node [#links] => Array ( [node-readmore] => Array ( [title] => Read more about Documenti - selezione 2025N64 [href] => node/126509 [html] => 1 [attributes] => Array ( [rel] => tag [title] => Documenti - selezione 2025N64 ) ) ) [#attributes] => Array ( [class] => Array ( [0] => links [1] => inline ) ) ) ) )

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