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Citing this Article

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Published on 27.09.17 in Vol 6, No 2 (2017): Jul-Dec

This paper is in the following e-collection/theme issue:

Works citing "Social Media and Multiple Sclerosis in the Posttruth Age"

According to Crossref, the following articles are citing this article (DOI 10.2196/ijmr.7879):

(note that this is only a small subset of citations)

  1. Díaz-Martín AM, Schmitz A, Yagüe Guillén MJ. Are Health e-Mavens the New Patient Influencers?. Frontiers in Psychology 2020;11
    CrossRef
  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
    CrossRef
  3. Farpour HR, Hoveidaei AH, 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
    CrossRef
  4. Tucker JD, Day S, Tang W, Bayus B. Crowdsourcing in medical research: concepts and applications. PeerJ 2019;7:e6762
    CrossRef
  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
    CrossRef
  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
    CrossRef
  7. Cárdenas-Robledo S, Navarro CE, Guío-Sánchez CM. Multiple sclerosis coverage in the written media of a low prevalence country. Multiple Sclerosis and Related Disorders 2020;44:102266
    CrossRef
  8. Tulloch JS, Vivancos R, Christley RM, Radford AD, Warner JC. 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
    CrossRef
  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
    CrossRef
  10. Rahn AC, 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
    CrossRef
  11. Martini M, Bragazzi NL. 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
    CrossRef
  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
    CrossRef
  13. Steijvers LCJ, Brinkhues S, Hoebe CJPA, van Tilburg TG, Claessen V, Bouwmeester-Vincken N, Hamers F, Vranken P, Dukers-Muijrers NHTM, 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
    CrossRef
  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
    CrossRef
  15. Alonso RN, Chertcoff A, Eizaguirre MB, Bauer J, Leguizamón F, Curbello MC, Cassará FP, Garcea O, Carrá A, Palma A, Silva BA. Decision making process in multiple sclerosis: An Argentine pilot study. Multiple Sclerosis and Related Disorders 2022;61:103751
    CrossRef
  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
    CrossRef
  17. Baucke CL, Seifert LS, 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
    CrossRef
  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
    CrossRef
  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)
    CrossRef
  20. Newsome SD, Binns C, Kaunzner UW, 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
    CrossRef
  21. Bevens W, Davenport R, Neate S, Yu M, Jelinek P, Jelinek GA, 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
    CrossRef