Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Silvia Potì

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Journal of Patient Experience|July 7, 2018
Subjective Experience of Illness Among Adolescents and Young Adults With Diabetes: A Qualitative Research StudySilvia Potì, Francesca Emiliani, Laura Palareti
Qualitative Health Research|August 4, 2011
Process of normalization in families with children affected by hemophiliaFrancesca Emiliani, Sabrina Bertocchi, Silvia Potì, et al.
Journal of Multidisciplinary Healthcare|June 14, 2019
Health care professionals dealing with hemophilia: insights from the international qualitative study of the HERO initiativeSilvia Potì, Laura Palareti, Frederica Rmy Cassis, et al.
Integrative Psychological & Behavioral Science|January 8, 2009
Mainstream economics and sense-makingSergio Salvatore, Guglielmo Forges Davanzati, Silvia Potì, et al.
International Journal of Qualitative Studies on Health and Well-Being|November 19, 2015
Shared topics on the experience of people with haemophilia living in the UK and the USA and the influence of individual and contextual variables: Results from the HERO qualitative studyLaura Palareti, Silvia Potì, Frederica Cassis, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of Patient Experience|July 7, 2018
Subjective Experience of Illness Among Adolescents and Young Adults With Diabetes: A Qualitative Research StudySilvia Potì, Francesca Emiliani, Laura Palareti
Qualitative Health Research|August 4, 2011
Process of normalization in families with children affected by hemophiliaFrancesca Emiliani, Sabrina Bertocchi, Silvia Potì, et al.
Journal of Multidisciplinary Healthcare|June 14, 2019
Health care professionals dealing with hemophilia: insights from the international qualitative study of the HERO initiativeSilvia Potì, Laura Palareti, Frederica Rmy Cassis, et al.
Integrative Psychological & Behavioral Science|January 8, 2009
Mainstream economics and sense-makingSergio Salvatore, Guglielmo Forges Davanzati, Silvia Potì, et al.
International Journal of Qualitative Studies on Health and Well-Being|November 19, 2015
Shared topics on the experience of people with haemophilia living in the UK and the USA and the influence of individual and contextual variables: Results from the HERO qualitative studyLaura Palareti, Silvia Potì, Frederica Cassis, et al.
Pageof 1