Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Ioana A Coman"'
This edited collection compares and analyses the most prominent political communicative responses to the outbreak and global spread of the COVID-19 strain of coronavirus within 27 nations across five continents and two supranational organisations: th
Publikováno v:
Frontiers in Sociology, Vol 8 (2023)
Facebook is the most popular social media platform and often used by news organizations to distribute content to broad audiences. Features of this online news environment, especially user-generated comments shown to news consumers, have the potential
Externí odkaz:
https://doaj.org/article/11a2a01fcd9a40dc9a2152a51dd70f58
It Is a Wild World in the City: Urban Wildlife Conservation and Communication in the Age of COVID-19
Publikováno v:
Diversity, Vol 14, Iss 7, p 539 (2022)
Most ecosystems are increasingly being degraded and reduced by human activities at the local and global scales. In contrast, urban environments are expanding as increasing portions of humanity move into cities. Despite the common perception among bio
Externí odkaz:
https://doaj.org/article/e99e57f4791c437d9cc1dfb34b36b57e
Publikováno v:
Health Communication. :1-10
Autor:
Jeanine P.D. Guidry, Lucinda L. Austin, Nicole H. O’Donnell, Ioana A. Coman, Alessandro Lovari, Marcus Messner
Publikováno v:
Journal of Primary Care & Community Health, Vol 11 (2020)
Influenza epidemics happen every year, with more than 8 million severe cases in 2017. The most effective way to prevent seasonal influenza is vaccination. In recent years, misinformation regarding vaccines abounds on social media, but the flu vaccine
Externí odkaz:
https://doaj.org/article/1a3bb95b63814ec7b8b0bc5eacc6674a
Autor:
Leah M. Mattiaccio, Ioana L. Coman, Carlie A. Thompson, Wanda P. Fremont, Kevin M. Antshel, Wendy R. Kates
Publikováno v:
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-11 (2018)
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental syndrome associated with deficits in cognitive and emotional processing. This syndrome represents one of the highest risk factors for the development of schizophrenia. Pr
Externí odkaz:
https://doaj.org/article/e9a40ef5493848ab98a540b0e3be5f60
Publikováno v:
American Journal of Health Promotion. 37:488-498
Purpose Drawing from the Health Belief Model, we explored how disadvantaged groups in the U.S., including Black, Hispanic, less educated and wealthy individuals, experienced perceived barriers and cues to action in the context of the COVID-19 vaccina
Religion, popular culture and social media: the construction of a religious leader image on Facebook
Autor:
Ioana A. COMAN, Mihai COMAN
Publikováno v:
Essachess, Vol 10, Iss 2, Pp 129-143 (2017)
Despite the emergence of religions on Internet and the importance of social media, research dedicated to religious leaders’ construction of symbolic image on social media, is hard to find. Starting from the 2013 Applebee’s social media crisis, wh
Externí odkaz:
https://doaj.org/article/0bd7e32888cf45aa9c08f077de963edc
Autor:
Daniel S. Tylee, Zora Kikinis, Thomas P. Quinn, Kevin M. Antshel, Wanda Fremont, Muhammad A. Tahir, Anni Zhu, Xue Gong, Stephen J. Glatt, Ioana L. Coman, Martha E. Shenton, Wendy R. Kates, Nikos Makris
Publikováno v:
NeuroImage: Clinical, Vol 15, Iss , Pp 832-842 (2017)
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a genetic neurodevelopmental syndrome that has been studied intensively in order to understand relationships between the genetic microdeletion, brain development, cognitive function, and the emergen
Externí odkaz:
https://doaj.org/article/cb3aa6b71cf44449a17b7e94312ce4eb
Autor:
Zora Kikinis, Nikos Makris, Valerie J. Sydnor, Sylvain Bouix, Ofer Pasternak, Ioana L. Coman, Kevin M. Antshel, Wanda Fremont, Marek R. Kubicki, Martha E. Shenton, Wendy R. Kates, Yogesh Rathi
Publikováno v:
NeuroImage: Clinical, Vol 21, Iss , Pp - (2019)
Background: 22q11.2 Deletion Syndrome (22q11DS) is a genetic, neurodevelopmental disorder characterized by a chromosomal deletion and a distinct cognitive profile. Although abnormalities in the macrostructure of the cortex have been identified in ind
Externí odkaz:
https://doaj.org/article/2e991f7cbbea483da395130efd2d5878