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Cited by in F6Publishing
For: Vyas J, Muirhead N, Singh R, Ephgrave R, Finlay AY. Impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the quality of life of people with ME/CFS and their partners and family members: an online cross-sectional survey. BMJ Open 2022;12:e058128. [PMID: 35501074 DOI: 10.1136/bmjopen-2021-058128] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Líška D, Liptaková E, Babičová A, Batalik L, Baňárová PS, Dobrodenková S. What is the quality of life in patients with long COVID compared to a healthy control group? Front Public Health 2022;10:975992. [PMID: 36408018 DOI: 10.3389/fpubh.2022.975992] [Reference Citation Analysis]
2 Araja D, Krumina A, Berkis U, Nora-krukle Z, Murovska M. The Advantages of an Integrative Approach in the Primary Healthcare of Post-COVID-19 and ME/CFS Patients. COVID-19 Pandemic, Mental Health and Neuroscience - New Scenarios for Understanding and Treatment [Working Title] 2022. [DOI: 10.5772/intechopen.106013] [Reference Citation Analysis]
3 O'Dwyer S, Boothby S, Smith G, Biddle L, Muirhead N, Khot S. Unpaid carers are the missing piece in treatment guidelines and research priorities for ME/CFS. BMJ 2022;378:o1691. [PMID: 35835467 DOI: 10.1136/bmj.o1691] [Reference Citation Analysis]