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Cinzia Colombo

Dados Biográficos

ID8979798
NOMECinzia Colombo
PRENOMESCinzia
SOBRENOMEColombo
ASSINATURACOLOMBO C
AFILIAÇÕESLaboratory for medical research and consumer involvement Department of Public Health IRCSS‐Mario Negri Institute for Pharmacological Research Milan Italy
ORCID0000-0001-6639-694X
VERIFICADOSim
TOTAL DE OBRAS2
TOTAL DE CITAÇÕES0
TOTAL COMO AUTOR2
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2007
ANO MAIS RECENTE DE PUBLICAÇÃO2016
ÍNDICE H0
  • Online health information seeking

    Open Access•Anneliese Synnot, Anneliese J Synnot et al.•ARTICLE•Health Expectations•2016

    BACKGROUND AND OBJECTIVE: The Internet is increasingly prominent as a source of health information for people with multiple sclerosis (MS). But there has been little exploration of the needs, experiences and preferences of people with MS for integrating treatment information into decision making, in the context of searching on the Internet. This was the aim of our study. DESIGN: Sixty participants (51 people with MS; nine family members) took par…

  • PartecipaSalute, an Italian project to involve lay people, patients’ associations and scientific‐medical representatives in the health debate

    Open Access•Paola Mosconi, Cinzia Colombo et al.•ARTICLE•Health Expectations•2007

    Consumers and patients are increasingly demanding an active role in health-care access and quality, and associations and pressure groups are interacting directly with national health services and with researchers, doctors and scientific or professional societies.1–4 This article describes an Italian project aimed at creating a partnership among lay people, patients’ associations and the scientific/medical community. In Italy, consumers are genera…

Sem obras proeminentes nesta página.

  • PartecipaSalute, an Italian project to involve lay people, patients’ associations and scientific‐medical representatives in the health debate

    Open Access•Paola Mosconi, Cinzia Colombo et al.•ARTICLE•Health Expectations•2007

    Consumers and patients are increasingly demanding an active role in health-care access and quality, and associations and pressure groups are interacting directly with national health services and with researchers, doctors and scientific or professional societies.1–4 This article describes an Italian project aimed at creating a partnership among lay people, patients’ associations and the scientific/medical community. In Italy, consumers are genera…

  • Online health information seeking

    Open Access•Anneliese Synnot, Anneliese J Synnot et al.•ARTICLE•Health Expectations•2016

    BACKGROUND AND OBJECTIVE: The Internet is increasingly prominent as a source of health information for people with multiple sclerosis (MS). But there has been little exploration of the needs, experiences and preferences of people with MS for integrating treatment information into decision making, in the context of searching on the Internet. This was the aim of our study. DESIGN: Sixty participants (51 people with MS; nine family members) took par…

General partnership (2 obras) · Health care (2 obras) · Psychology (2 obras) · Business (1 obras) · Computer Science (1 obras) · Empathy and Medical Education (1 obras) · Empowerment (1 obras) · Focus group (1 obras) · Health information (1 obras) · Health Literacy and Information Accessibility (1 obras)

Ethnos_APP • Projeto Open Source • Licença MIT • Frontend v2.0.0 • Privacidade e Cookies • Documentação da API: api.ethnos.app/docs • Código da API: GitHub • DOI: 10.5281/zenodo.17049435 • Código do Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae