Published on in Vol 6, No 2 (2017): Jul-Dec

Social Media and Multiple Sclerosis in the Posttruth Age

Social Media and Multiple Sclerosis in the Posttruth Age

Social Media and Multiple Sclerosis in the Posttruth Age

Journals

  1. Díaz-Martín A, Schmitz A, Yagüe Guillén M. Are Health e-Mavens the New Patient Influencers?. Frontiers in Psychology 2020;11 View
  2. Lavorgna L, Brigo F, Moccia M, Leocani L, Lanzillo R, Clerico M, Abbadessa G, Schmierer K, Solaro C, Prosperini L, Tedeschi G, Giovannoni G, Bonavita S. e-Health and multiple sclerosis: An update. Multiple Sclerosis Journal 2018;24(13):1657 View
  3. Farpour H, Hoveidaei A, Habibi L, Moosavi M, Farpour S. The impact of social media use on depression in multiple sclerosis patients. Acta Neurologica Belgica 2020;120(6):1405 View
  4. Tucker J, Day S, Tang W, Bayus B. Crowdsourcing in medical research: concepts and applications. PeerJ 2019;7:e6762 View
  5. Yeandle D, Rieckmann P, Giovannoni G, Alexandri N, Langdon D. Patient Power Revolution in Multiple Sclerosis: Navigating the New Frontier. Neurology and Therapy 2018;7(2):179 View
  6. Lavorgna L, Borriello G, Esposito S, Abbadessa G, Capuano R, De Giglio L, Logoteta A, Pozzilli C, Tedeschi G, Bonavita S. Impact of early diagnosis on clinical characteristics of an Italian sample of people with multiple sclerosis recruited online. Multiple Sclerosis and Related Disorders 2019;27:239 View
  7. Cárdenas-Robledo S, Navarro C, Guío-Sánchez C. Multiple sclerosis coverage in the written media of a low prevalence country. Multiple Sclerosis and Related Disorders 2020;44:102266 View
  8. Tulloch J, Vivancos R, Christley R, Radford A, Warner J. Mapping tweets to a known disease epidemiology; a case study of Lyme disease in the United Kingdom and Republic of Ireland. Journal of Biomedical Informatics 2019;100:100060 View
  9. Brigo F, Lattanzi S, Giussani G, Tassi L, Pietrafusa N, Galimberti C, Bragazzi N, Mecarelli O. A cross-sectional survey among physicians on internet use for epilepsy-related information. Epilepsy Research 2020;165:106393 View
  10. Rahn A, Solari A, Beckerman H, Nicholas R, Wilkie D, Heesen C, Giordano A. “I Will Respect the Autonomy of My Patient”. International Journal of MS Care 2020;22(6):285 View
  11. Martini M, Bragazzi N. Googling for Neurological Disorders: From Seeking Health-Related Information to Patient Empowerment, Advocacy, and Open, Public Self-Disclosure in the Neurology 2.0 Era. Journal of Medical Internet Research 2021;23(3):e13999 View
  12. Lavorgna L, Brigo F, Esposito S, Abbadessa G, Sparaco M, Lanzillo R, Moccia M, Inglese M, Bonfanti L, Trojsi F, Spina E, Russo A, De Micco P, Clerico M, Tedeschi G, Bonavita S. Public Engagement and Neurology: An Update. Brain Sciences 2021;11(4):429 View
  13. Steijvers L, Brinkhues S, Hoebe C, van Tilburg T, Claessen V, Bouwmeester-Vincken N, Hamers F, Vranken P, Dukers-Muijrers N, Lavorgna L. Social networks and infectious diseases prevention behavior: A cross-sectional study in people aged 40 years and older. PLOS ONE 2021;16(5):e0251862 View
  14. Kant R, Varea R, Titifanue J. COVID-19 vaccine online misinformation in Fiji: Preliminary findings. Pacific Journalism Review : Te Koakoa 2021;27(1and2):47 View
  15. Alonso R, Chertcoff A, Eizaguirre M, Bauer J, Leguizamón F, Curbello M, Cassará F, Garcea O, Carrá A, Palma A, Silva B. Decision making process in multiple sclerosis: An Argentine pilot study. Multiple Sclerosis and Related Disorders 2022;61:103751 View
  16. Isomursu M, Kuoremäki R, Eho J, Teikari M. The effect of Covid-19 in digital media use of Finnish physicians – Four wave longitudinal panel survey. International Journal of Medical Informatics 2022;159:104677 View
  17. Baucke C, Seifert L, Kaelber K, Lavorgna L. Health co-inquiry in migraine: Online participation and stakeholder experiences before and during the COVID-19 pandemic. PLOS ONE 2021;16(11):e0260376 View
  18. Mutambik I, Lee J, Almuqrin A, Halboob W, Omar T, Floos A, Lavorgna L. User concerns regarding information sharing on social networking sites: The user’s perspective in the context of national culture. PLOS ONE 2022;17(1):e0263157 View
  19. SULLO A, PICCIOCCHI E, FERRANTE L. Multiple sclerosis: medical-legal assessment guidelines in the welfare and social security field. Minerva Forensic Medicine 2022;142(2-3) View
  20. Newsome S, Binns C, Kaunzner U, Morgan S, Halper J. No Evidence of Disease Activity (NEDA) as a Clinical Assessment Tool for Multiple Sclerosis: Clinician and Patient Perspectives [Narrative Review]. Neurology and Therapy 2023;12(6):1909 View
  21. Bevens W, Davenport R, Neate S, Yu M, Jelinek P, Jelinek G, Reece J. Web-Based Health Information Seeking by People Living With Multiple Sclerosis: Qualitative Investigation of the Multiple Sclerosis Online Course. Journal of Medical Internet Research 2024;26:e53372 View