Trasparenza DDG Rep. n. 3765/2023 Prot. n. 184079 del 26/09/2023 con oggetto "Rivalutazione e determinazione valorizzazione economica della posizione organizzativa di Direttore dell’Ufficio Eventi Permanenti dell’Area Comunicazione e Marketing – ACoM”

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Arqus moVEs - 1a edizione

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Arqus annuncia la nuova edizione di Arqus moVEs, un virtual exchange dedicato a tutte le studentesse e gli studenti che devono iniziare una mobilità internazionale nel secondo semestre dell'anno accademico 23/24. Il programma è aperto anche a tutte e tutti coloro che non hanno ancora avuto la possibilità di andare all'estero per studio ma vogliono comunque vivere un'esperienza interculturale e multilinguistica.

Affrontando temi di interesse globale e creando spazi di confronto tra culture, lingue e profili universitari diversi si potranno  perfezionare quelle soft skill necessarie ad affrontare  sia le sfide internazionali che le dinamiche sempre più globali della vita quotidiana. Il progetto prevede modalità diverse:

many-to-many: spazi comunicativi in cui varie lingue verranno utilizzate oltre all'inglese come linguae francae

few-to-few: spazi per attività collaborative

Il progetto si svolge nei mesi precedenti alla partenza delle mobilità, ha una durata di 8-10 settimane e prevede un carico di lavoro di circa 2-3 ore a settimana. Sono previste attività in modalità sincrona e asincrona.

Alle studentesse e agli studenti che rispetteranno i requisiti del programma verrà riconosciuto un badge, un attestato di partecipazione e un attestato di merito per coloro i quali si distinguano in termini di impegno e di partecipazione attiva.

 

Gli studenti che hanno partecipato all'edizione pilota di Arqus moVEs ci hanno raccontato la loro esperienza, ecco alcune testimonianze:

Faithful “...the actual program still managed to surprise and amaze me with its depth and breadth…it introduced me to a world of possibilities, inspiring an insatiable curiosity for culture”.

Diletta: “The idea behind it is impressive…”

Violeta: “...it’s undoubtedly a truly enriching and transformative experience…

arqus moVEs quotes

 

Arqus moVEs è aperto a tutte le studentesse e gli studenti degli atenei Arqus ma con un numero limitato di posti. Le studentesse e gli studenti saranno selezionati in base alla lettera di motivazione e alle esperienze pregresse.

Per maggiori informazioni consulta l'infografica qui sotto e visita il sito dell'Alleanza per iscriverti.

La deadline per le iscrizioni è prolungata al 31 ottobre ore 13:00.

Per qualunque informazione contatta moves@arqus-alliance.eu

 


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

Arqus annuncia la nuova edizione di Arqus moVEs, un virtual exchange dedicato a tutte le studentesse e gli studenti che devono iniziare una mobilità internazionale nel secondo semestre dell'anno accademico 23/24. Il programma è aperto anche a tutte e tutti coloro che non hanno ancora avuto la possibilità di andare all'estero per studio ma vogliono comunque vivere un'esperienza interculturale e multilinguistica.

Affrontando temi di interesse globale e creando spazi di confronto tra culture, lingue e profili universitari diversi si potranno  perfezionare quelle soft skill necessarie ad affrontare  sia le sfide internazionali che le dinamiche sempre più globali della vita quotidiana. Il progetto prevede modalità diverse:

many-to-many: spazi comunicativi in cui varie lingue verranno utilizzate oltre all'inglese come linguae francae

few-to-few: spazi per attività collaborative

Il progetto si svolge nei mesi precedenti alla partenza delle mobilità, ha una durata di 8-10 settimane e prevede un carico di lavoro di circa 2-3 ore a settimana. Sono previste attività in modalità sincrona e asincrona.

Alle studentesse e agli studenti che rispetteranno i requisiti del programma verrà riconosciuto un badge, un attestato di partecipazione e un attestato di merito per coloro i quali si distinguano in termini di impegno e di partecipazione attiva.

 

Gli studenti che hanno partecipato all'edizione pilota di Arqus moVEs ci hanno raccontato la loro esperienza, ecco alcune testimonianze:

Faithful “...the actual program still managed to surprise and amaze me with its depth and breadth…it introduced me to a world of possibilities, inspiring an insatiable curiosity for culture”.

Diletta: “The idea behind it is impressive…”

Violeta: “...it’s undoubtedly a truly enriching and transformative experience…

arqus moVEs quotes

 

Arqus moVEs è aperto a tutte le studentesse e gli studenti degli atenei Arqus ma con un numero limitato di posti. Le studentesse e gli studenti saranno selezionati in base alla lettera di motivazione e alle esperienze pregresse.

Per maggiori informazioni consulta l'infografica qui sotto e visita il sito dell'Alleanza per iscriverti.

La deadline per le iscrizioni è prolungata al 31 ottobre ore 13:00.

Per qualunque informazione contatta moves@arqus-alliance.eu

 


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Arqus annuncia la nuova edizione di Arqus moVEs, un virtual exchange dedicato a tutte le studentesse e gli studenti che devono iniziare una mobilità internazionale nel secondo semestre dell'anno accademico 23/24. Il programma è aperto anche a tutte e tutti coloro che non hanno ancora avuto la possibilità di andare all'estero per studio ma vogliono comunque vivere un'esperienza interculturale e multilinguistica.

Affrontando temi di interesse globale e creando spazi di confronto tra culture, lingue e profili universitari diversi si potranno  perfezionare quelle soft skill necessarie ad affrontare  sia le sfide internazionali che le dinamiche sempre più globali della vita quotidiana. Il progetto prevede modalità diverse:

many-to-many: spazi comunicativi in cui varie lingue verranno utilizzate oltre all'inglese come linguae francae

few-to-few: spazi per attività collaborative

Il progetto si svolge nei mesi precedenti alla partenza delle mobilità, ha una durata di 8-10 settimane e prevede un carico di lavoro di circa 2-3 ore a settimana. Sono previste attività in modalità sincrona e asincrona.

Alle studentesse e agli studenti che rispetteranno i requisiti del programma verrà riconosciuto un badge, un attestato di partecipazione e un attestato di merito per coloro i quali si distinguano in termini di impegno e di partecipazione attiva.

 

Gli studenti che hanno partecipato all'edizione pilota di Arqus moVEs ci hanno raccontato la loro esperienza, ecco alcune testimonianze:

Faithful “...the actual program still managed to surprise and amaze me with its depth and breadth…it introduced me to a world of possibilities, inspiring an insatiable curiosity for culture”.

Diletta: “The idea behind it is impressive…”

Violeta: “...it’s undoubtedly a truly enriching and transformative experience…

arqus moVEs quotes

 

Arqus moVEs è aperto a tutte le studentesse e gli studenti degli atenei Arqus ma con un numero limitato di posti. Le studentesse e gli studenti saranno selezionati in base alla lettera di motivazione e alle esperienze pregresse.

Per maggiori informazioni consulta l'infografica qui sotto e visita il sito dell'Alleanza per iscriverti.

La deadline per le iscrizioni è prolungata al 31 ottobre ore 13:00.

Per qualunque informazione contatta moves@arqus-alliance.eu

 


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

Arqus annuncia la nuova edizione di Arqus moVEs, un virtual exchange dedicato a tutte le studentesse e gli studenti che devono iniziare una mobilità internazionale nel secondo semestre dell'anno accademico 23/24. Il programma è aperto anche a tutte e tutti coloro che non hanno ancora avuto la possibilità di andare all'estero per studio ma vogliono comunque vivere un'esperienza interculturale e multilinguistica.

Affrontando temi di interesse globale e creando spazi di confronto tra culture, lingue e profili universitari diversi si potranno  perfezionare quelle soft skill necessarie ad affrontare  sia le sfide internazionali che le dinamiche sempre più globali della vita quotidiana. Il progetto prevede modalità diverse:

many-to-many: spazi comunicativi in cui varie lingue verranno utilizzate oltre all'inglese come linguae francae

few-to-few: spazi per attività collaborative

Il progetto si svolge nei mesi precedenti alla partenza delle mobilità, ha una durata di 8-10 settimane e prevede un carico di lavoro di circa 2-3 ore a settimana. Sono previste attività in modalità sincrona e asincrona.

Alle studentesse e agli studenti che rispetteranno i requisiti del programma verrà riconosciuto un badge, un attestato di partecipazione e un attestato di merito per coloro i quali si distinguano in termini di impegno e di partecipazione attiva.

 

Gli studenti che hanno partecipato all'edizione pilota di Arqus moVEs ci hanno raccontato la loro esperienza, ecco alcune testimonianze:

Faithful “...the actual program still managed to surprise and amaze me with its depth and breadth…it introduced me to a world of possibilities, inspiring an insatiable curiosity for culture”.

Diletta: “The idea behind it is impressive…”

Violeta: “...it’s undoubtedly a truly enriching and transformative experience…

arqus moVEs quotes

 

Arqus moVEs è aperto a tutte le studentesse e gli studenti degli atenei Arqus ma con un numero limitato di posti. Le studentesse e gli studenti saranno selezionati in base alla lettera di motivazione e alle esperienze pregresse.

Per maggiori informazioni consulta l'infografica qui sotto e visita il sito dell'Alleanza per iscriverti.

La deadline per le iscrizioni è prolungata al 31 ottobre ore 13:00.

Per qualunque informazione contatta moves@arqus-alliance.eu

 


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Arqus annuncia la nuova edizione di Arqus moVEs, un virtual exchange dedicato a tutte le studentesse e gli studenti che devono iniziare una mobilità internazionale nel secondo semestre dell'anno accademico 23/24. Il programma è aperto anche a tutte e tutti coloro che non hanno ancora avuto la possibilità di andare all'estero per studio ma vogliono comunque vivere un'esperienza interculturale e multilinguistica.

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PROVVISORIA - Legenda Graduatorie provvisorie Borse di studio regionali 2023/2024

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PROVVISORIA -Graduatorie provvisorie Borse di studio regionali 2023/2024

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Infografica Arqus moVEs

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2023S33 Quesiti colloquio

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2023S33 Quesiti prova scritta

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2023T41 Esito prova scritta - candidati ammessi al colloquio

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2023S33 Criteri di valutazione

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Fondazione Telethon finances 6 research projects based in Padua

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Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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

Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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

Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

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Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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

Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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

Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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

Dedicated to the best scientific research into rare genetic conditions, Fondazione Telethon announces the winner of the second round of its multi-round Call for research projects 2021-2024. With over 4.3 million euros raised thanks to donations, the foundation will fund 24 research projects throughout Italy, of which six are from Padua.

Winning research projects based in Padua include:

Nicoletta Plotegher (University of Padua) will lead the research on Gaucher’s disease. Categorized as a lysosomal storage disorder, Gaucher’s disease is an inherited metabolic disorder in which deficiency of the enzyme glucocerebrosidase (GCase) results in the accumulation of harmful quantities of certain fats.

Alessandro Carrer (University of Padua Department of Biology and Veneto Institute of Molecular Medicine) will lead a study on Niemann-Pick type C disease (NPCD). With no known cure and characterized by severe neurological symptoms, NPCD is a genetic disease caused by mutations in the NPC1 gene.

Massimo Zeviani (University of Padua) will lead the research on Mitochondrial DNA (mtDNA) depletion syndromes (MDS), which include a group of mitochondrial diseases characterized by mtDNA instability. In particular, the research focuses on mitochondrial DNA (mtDNA) depletion in the liver and brain (neuro-hepatopathy).

Nina Kaludercic (University of Padua) will focus on the study of cardiomyopathy associated with Duchenne muscular dystrophy (DMD), a rare hereditary disease that involves progressive degeneration of muscle tissue.

Ildiko Szabo (University of Padua) will lead the research on mitochondrial diseases. As rare genetic diseases, mitochondrial dysfunction affects organs and tissues, such as the brain and muscle, and are associated with a wide range of clinical presentations ranging from movement disorders to growth retardation and early death.

Claudia Lodovichi (National Research Council - CNR Padua), will lead the research on the molecular mechanisms underlying the deficits in social behavior and cognitive functions associated with autism spectrum disorders.

Telethon’s multi-round Call for research projects consists of four different rounds, corresponding to four specific deadlines. With Basic Research and Preclinical Proof of Concept tracks, applicants can apply to one track per round, with one research project. Each round and track will have a dedicated peer review process and competition. For those who wish to apply, the submission deadline for the 3rd round is October 31, 2023.

 


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