Information system

All Items

• Study protocol: evaluation of a pharmaceutical intervention for safe use of medications in patients with liver cirrhosis e202601004

  Andrea Rodríguez Esquíroz, Amaya Echeverría Gorriti, Marta Marín Marín, Lorea Sanz Álvarez, Patricia García González, Javier Gorricho Mendívil, Juan Isidro Uriz Otano, Javier Garjón Parra, Inés Aguinaga Ontoso

  13 páginas

• Predictive factors of survival in people with Cystic fibrosis from a Spanish registry of rare diseases e202508042

  Senay Rueda Nieto, Pedro Mondejar-Lopez, María-Pilar Mira-Escolano, Ana Cutillas-Tolín, Luis Alberto Maceda-Roldán, Julián Jesús Arense-Gonzalo, Joaquín A. Palomar-Rodríguez

  17 páginas

• Prevalence of Hereditary Hemorrhagic Telangiectasia: a population-based study in the Valencian region (Spain) e202311096

  Miriam de la Natividad Palomares, Laia Barrachina-Bonet, Laura García-Villodre, Sandra Guardiola-Vilarroig, Óscar Zurriaga Llorens, Clara Cavero-Carbonell

  11 páginas

• Notification and Learning System for Patient Safety (SiNASP): Current situation in Ferrol Primary Care e202112193

  Bruno Castro Matesanz, Eva Tizón-Bouza, José Ángel Pesado-Cartelle

  11 páginas

• Surveillance of rare diseases in Spain: Spanish Registry of Rare Diseases (ReeR) e202111186

  Esther Vicente, Eva Ardanaz, Enrique Ramalle-Gómara, Luis J. Echevarría, M. Pilar Mira, Juan Pablo Chalco-Orrego, Consuelo Benito, Sandra Guardiola-Vilarroig, Cristina Mallol, José Manuel Guinaldo, Patricia Carrillo, Mercedes Cáffaro, M. Luisa Compés, M. Nieves Caro, Verónica Alonso, Pilar Soler, Grupo de Trabajo del Registro Estatal de Enfermedades Raras (GT-ReeR)

  18 páginas

• Role of the information systems and e-health in the COVID-19 pandemic. A call to action e202101006

  Almudena Martín Fernández

  15 páginas

• Implementing a population-based rare diseases registry in Spain: Navarre´s experience e201811082

  Esther Vicente, Marcela Guevara, María J. Lasanta, María A. Ramos-Arroyo, Eva Ardanaz

  13 páginas