European Project for Rare Diseases National Plans Development (EUROPLAN)

af Taruscio, Domenica, Vittozzi, Luciano
Udgivet 2010

The Italian National Rare Diseases Registry

af Taruscio, Domenica, Kodra, Yllka, Ferrari, Gianluca, Vittozzi, Luciano
Udgivet 2014

Evaluation of population newborn screening practices for rare disorders in member states of the European Union

af Vittozzi, Luciano, Hoffmann, Georg F, Cornel, Martina, Loeber, Gerard
Udgivet 2010

The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases

af Taruscio, Domenica, Vittozzi, Luciano, Rocchetti, Adele, Torreri, Paola, Ferrari, Luca
Udgivet i Int J Environ Res Public Health (2018)

EPIRARE survey on activities and needs of rare disease registries in the European Union

af Taruscio, Domenica, Gainotti, Sabina, Vittozzi, Luciano, Bianchi, Fabrizio, Ensini, Monica, Posada, Manuel
Udgivet 2012

The EPIRARE proposal of a set of indicators and common data elements for the European platform for rare disease registration

af Taruscio, Domenica, Mollo, Emanuela, Gainotti, Sabina, Posada de la Paz, Manuel, Bianchi, Fabrizio, Vittozzi, Luciano
Udgivet 2014

Current status of Italian Registries on inherited bleeding disorders

af Hassan, Hamisa Jane, Morfini, Massimo, Taruscio, Domenica, Abbonizio, Francesca, Giampaolo, Adele, Kodra, Yllka, Oliovecchio, Emily, Vittozzi, Luciano
Udgivet 2014

Characterization and classification of Rare Disease Registries by using exploratory data analyses

af Coi, Alessio, Santoro, Michele, Lipucci, Michele, Bianucci, Anna Maria, Gainotti, Sabina, Mollo, Emanuela, Vittozzi, Luciano, Taruscio, Domenica, Bianchi, Fabrizio
Udgivet i Orphanet J Rare Dis (2014)

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

af Cornel, Martina C, Rigter, Tessel, Weinreich, Stephanie S, Burgard, Peter, Hoffmann, Georg F, Lindner, Martin, Gerard Loeber, J, Rupp, Kathrin, Taruscio, Domenica, Vittozzi, Luciano
Udgivet 2014

The Italian National Centre for Rare Diseases: where research and public health translate into action

af Taruscio, Domenica, Agresta, Linda, Amato, Annalisa, Bernardo, Giuseppe, Bernardo, Luana, Braguti, Francesca, Carbone, Pietro, Carta, Claudio, Ceccarini, Marina, Censi, Federica, Coppola, Simona, Crialese, Patrizia, De Santis, Marta, Diemoz, Stefano, Donati, Carlo, Gainotti, Sabina, Ferrari, Gianluca, Floridia, Giovanna, Frank, Claudio, Frazzica, Rosa Giuseppa, Gentile, Amalia E., Granata, Orietta, Kodra, Yllka, Latrofa, Manuela, Laricchiuta, Paola, Magrelli, Armando, Morciano, Cristina, Polizzi, Agata, Razeto, Stefania, Salvatore, Marco, Sanseverino, Antonella, Savini, Daniele, Torreri, Paola, Tosto, Fabrizio, Villani, Flavia, Vincenti, Giorgio, Vittozzi, Luciano
Udgivet 2014