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sunnquist

  1. Andy
    Thread

    Rethinking the Standard of Care for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2019, Friedberg, Sunnquist and Nacul

    For over two decades, the standard of care for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) has been cognitive behavior therapy...
    Thread by: Andy, Oct 23, 2019, 26 replies, in forum: ME/CFS research
  2. Andy
    Thread

    The DePaul Symptom Questionnaire-2: a validation study, 2019, Sunnquist et al

    Background: The DePaul Symptom Questionnaire (DSQ) was developed to assess the symptomatology and case definition fulfillment of individuals with...
    Thread by: Andy, Sep 13, 2019, 8 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  3. John Mac
    Thread

    Defining the prevalence and symptom burden of those with self-reported severe CFS/ME: a ... community pilot study... (2017) Strassheim et al

    Objectives To define the prevalence of severe chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) and its clinical characteristics in a...
    Thread by: John Mac, Sep 20, 2018, 26 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  4. Dolphin
    Thread

    Latent class analysis of a heterogeneous international sample of patients with myalgic encephalomyelitis/chronic fatigue syndrome (Leonard Jason team)

    https://www.tandfonline.com/doi/full/10.1080/21641846.2018.1494530 Original Articles Latent class analysis of a...
    Thread by: Dolphin, Jul 4, 2018, 40 replies, in forum: ME/CFS research
  5. Dolphin
    Thread

    Devendorf et al. 2017 Defining and measuring recovery from myalgic encephalomyelitis and chronic fatigue syndrome: the physician perspective

    http://www.tandfonline.com/doi/abs/10.1080/09638288.2017.1383518 Original Article Defining and measuring recovery from myalgic encephalomyelitis...
    Thread by: Dolphin, Nov 8, 2017, 10 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
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