Sam Carter
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Sam Carter (Samuel Carter) is an advocate and a patient with myalgic encephalomyelitis.
Talks and interviews[edit | edit source]
Letters[edit | edit source]
- 2010 - FINE trial for CFS. Both significant and small?[1]
- 2012 - A valedictory dispatch from the Psychosocial School?[2]
- 2016 - Exploring changes to PACE trial outcome measures using anonymised data from the FINE trial[3]
Online presence[edit | edit source]
- Website/Blog
- YouTube
See also[edit | edit source]
Learn more[edit | edit source]
- Wikipedia
References[edit | edit source]
- ↑ Carter, Sam (June 9, 2010). "FINE Trial for CFS: Both significant and small?". BMJ. 340: c2988. doi:10.1136/bmj.c2988. ISSN 0959-8138. PMID 20534659.
- ↑ Carter, Sam (May 5, 2012). "A valedictory dispatch from the Psychosocial School? | Rapid Responses to articles". BMJ. Retrieved January 29, 2019. Cite has empty unknown parameter:
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(help) - ↑ Carter, Sam (February 15, 2016). "Exploring changes to PACE trial outcome measures using anonymised data from the FINE trial". PubMed Commons. Archived from the original on February 2016. Unknown parameter
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