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1 ome), and malaise/fatigue (including chronic fatigue syndrome).
2 ostpoliomyelitis, poststroke, and in chronic fatigue syndrome.
3 gnostic criteria for neurasthenia or chronic fatigue syndrome.
4 the current state of knowledge about chronic fatigue syndrome.
5 oes not seem to be beneficial in the chronic fatigue syndrome.
6 relaxation therapy for patients with chronic fatigue syndrome.
7 tant in both chronic fatigue and the chronic fatigue syndrome.
8 There is mild hypocortisolism in chronic fatigue syndrome.
9 ctor contributing to the symptoms of chronic fatigue syndrome.
10 of well-characterized patients with chronic fatigue syndrome.
11 such as irritable bowel syndrome and chronic fatigue syndrome.
12 drome, heat intolerance, and perhaps chronic fatigue syndrome.
13 hysical disability for patients with chronic fatigue syndrome.
14 documented in both fibromyalgia and chronic fatigue syndrome.
15 documented in both fibromyalgia and chronic fatigue syndrome.
16 virus and Still's disease as well as chronic fatigue syndrome.
17 ic stress disorder, and possibly the chronic fatigue syndrome.
18 tibodies in sera of 60 patients with chronic fatigue syndrome.
19 dence for an autoimmune component in chronic fatigue syndrome.
20 bilitating symptoms of patients with chronic fatigue syndrome.
21 osis in the bigger context of the post-viral fatigue syndrome.
22 during the acute phase leading to post-viral fatigue syndrome.
23 cidality adequately in patients with chronic fatigue syndrome.
24 e entry) and received a diagnosis of chronic fatigue syndrome.
25 T and SMC plus GET for patients with chronic fatigue syndrome.
26 apy (APT) plus SMC and SMC alone for chronic fatigue syndrome.
27 rpetuating fatigue and disability in chronic fatigue syndrome.
28 iating symptoms of depression and in chronic fatigue syndrome.
29 vation approached levels observed in chronic fatigue syndrome.
30 le bowel syndrome, fibromyalgia, and chronic fatigue syndrome.
31 iated with human prostate cancer and chronic fatigue syndrome.
32 able to previously described post-infectious fatigue syndrome.
33 medical care (SMC) for patients with chronic fatigue syndrome.
34 ation with human prostate cancer and chronic fatigue syndrome.
35 rus linked to prostate carcinoma and chronic fatigue syndrome.
36 n the human gammaretrovirus XMRV and chronic fatigue syndrome.
37 r postinfectious irritable bowel and chronic fatigue syndromes.
38 logical distress in chronic pain and chronic fatigue syndromes.
39 attributable to the chronic pain and chronic fatigue syndromes.
40 prostate cancer and in patients with chronic fatigue syndromes.
43 athy, 463; myalgic encephalomyelitis/chronic fatigue syndrome, 95; preload failure, 120; post-treatme
46 ation with human prostate cancer and chronic fatigue syndrome, although these associations are contro
47 s meeting international criteria for chronic fatigue syndrome and 329 participants meeting London cri
48 121 consecutive clinic patients with chronic fatigue syndrome and 64 comparison subjects without the
50 confirmed an association between the chronic fatigue syndrome and orthostatic intolerance; however, t
51 l microbiome have been identified in chronic fatigue syndrome and other neuropsychiatric disorders, a
52 ymptoms of myalgic encephalomyelitis/chronic fatigue syndrome and other post-acute infectious syndrom
53 es such as myalgic encephalomyelitis/chronic fatigue syndrome and postural orthostatic tachycardia sy
54 es such as myalgic encephalomyelitis/chronic fatigue syndrome and postural orthostatic tachycardia sy
55 coronary heart disease, cancer, and chronic fatigue syndrome and those remaining on their initial re
56 sought predictors of both acute and chronic fatigue syndromes and mood disorders from clinical, labo
57 ine and fibromyalgia', 'Dopamine and chronic fatigue syndrome' and 'Dopamine and irritable bowel synd
58 clear envelope proteins was found in chronic fatigue syndrome, and an increased prevalence of antipol
59 ssants for irritable bowel syndrome, chronic fatigue syndrome, and chronic back pain were selected fo
60 iated with type I diabetes, obesity, chronic fatigue syndrome, and various manifestations of inflamma
62 C to moderately improve outcomes for chronic fatigue syndrome, but APT is not an effective addition.
63 an effective and safe treatment for chronic fatigue syndrome, but it is therapist intensive and avai
64 d all-cause mortality in people with chronic fatigue syndrome, but our findings show a substantial in
65 GET) can be effective treatments for chronic fatigue syndrome, but patients' organisations have repor
66 in blood samples from patients with chronic fatigue syndrome, but these findings have not been repli
69 rlapping with those characterised as chronic fatigue syndrome (CFS) and have been described as CFS-li
70 1994 criteria were used to diagnose chronic fatigue syndrome (CFS) and idiopathic chronic fatigue (I
73 in the blood of 67% of patients with chronic fatigue syndrome (CFS) compared with 3.7% of healthy con
74 nt reports showed many patients with chronic fatigue syndrome (CFS) harbor a retrovirus, xenotropic m
79 sorder (PTSD) and illness resembling chronic fatigue syndrome (CFS) in the entire population of Gulf
89 is of myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS) is based on clinical criteria, ye
92 Das Gupta, analyzed DNA samples from chronic fatigue syndrome (CFS) patients and healthy controls.
93 ifferences in the immune function of chronic fatigue syndrome (CFS) patients are detectable in rigoro
96 te sinusitis (n = 25), subjects with chronic fatigue syndrome (CFS) with nonallergic rhinitis (n = 14
112 s were recruited from six specialist chronic fatigue syndrome clinics in the UK National Health Servi
113 understanding the pathophysiology of chronic fatigue syndrome continue to demonstrate the involvement
114 o, 2.32 [95% CI, 1.02 to 5.27]); the chronic fatigue syndrome (deployed, 1.6%; nondeployed 0.1%; odds
115 measures included fibromyalgia, the chronic fatigue syndrome, dermatologic conditions, dyspepsia, ph
120 lth and Care Excellence criteria for chronic fatigue syndrome from two secondary-care clinics in the
122 Turner syndrome, Williams syndrome, chronic fatigue syndrome, IgA nephropathy, and IgA deficiency.
123 12 as part of the Norwegian Study of Chronic Fatigue Syndrome in Adolescents: Pathophysiology and Int
124 tality in individuals diagnosed with chronic fatigue syndrome in secondary and tertiary care using da
125 m', 'Functional somatic syndromes', 'Chronic fatigue syndrome', 'Irritable bowel syndrome', 'Fibromya
127 across many domains, suggesting that chronic fatigue syndrome is a heterogeneous condition of complex
136 Reports of mild hypocortisolism in chronic fatigue syndrome led us to postulate that low-dose hydro
137 erception of health as fair or poor, chronic fatigue syndrome-like illness, and posttraumatic stress
139 yalgic encephalomyelitis also called chronic fatigue syndrome linked to a viral and autoimmune pathog
140 I) such as Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, Long-COVID, and Gulf War Illness (GWI)
143 essment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (MCAM), we relied on expert clinician d
145 esearch of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia (FM), two acq
146 ID (LC), Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) and healthy control subjects.
148 iving with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) experience heterogeneous and d
149 es such as myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) have long been linked to infec
166 tiology of myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is unknown, but involvement of
168 GO-ME/CFS) myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) manifest similar symptoms, it
170 agement of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), a disabling long-term conditi
171 tures with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), suggest the potential involve
172 ts with myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS), the data are limited and cont
173 with PASC, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), though studies have yielded m
182 chizophrenia (SZ), anxiety disorder, chronic fatigue syndrome, multiple sclerosis, amyotrophic latera
185 is marketed as a diagnostic test for chronic fatigue syndrome/Myalgic Encephalomyelitis (CFS/ME).
186 the following 5 groups of patients: chronic fatigue syndrome (n = 32), human immunodeficiency virus
187 nesis of non-GI autoimmune diseases, chronic fatigue syndrome, obesity and even some neuropsychiatric
188 ation between XMRV and patients with chronic fatigue syndrome or chronic immunomodulatory conditions.
191 ssociated syncope, eating disorders, chronic fatigue syndrome, or history of congenital heart disease
193 infectious myalgic encephalomyelitis/chronic fatigue syndrome (PI-ME/CFS) is a disabling disorder, ye
194 n-diagnosed multisymptom conditions: chronic fatigue syndrome, posttraumatic stress disorder, multipl
196 cancer and myalgic encephalomyelitis/chronic fatigue syndrome, recent data indicate that results inte
197 ificantly lower in the subjects with chronic fatigue syndrome regardless of the presence or absence o
198 way in which chronic fatigue and the chronic fatigue syndrome relate to each other: Is one the severe
199 virus (XMRV) in prostate cancer and chronic fatigue syndrome reported in previous studies remains co
201 The assessment and treatment of chronic fatigue syndrome should be multidimensional and tailored
202 increased risk for fibromyalgia, the chronic fatigue syndrome, skin conditions, dyspepsia, and a clin
204 health, or had a history of obesity, chronic fatigue syndrome, substance abuse, an eating disorder, o
205 T cells and B cells of patients with chronic fatigue syndrome, suggesting an association between XMRV
206 ed whether narrow definitions of unexplained fatigue syndromes that require additional minor somatic
208 War syndrome, chronic whiplash, the chronic fatigue syndrome, the irritable bowel syndrome, and fibr
210 MRV, in blood cells of patients with chronic fatigue syndrome," two of the coauthors, Silverman and D
212 esearch on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome was cosponsored by the NIH Office of Di
213 herapy versus relaxation therapy for chronic fatigue syndrome were invited to complete self-rated mea
214 patients meeting Oxford criteria for chronic fatigue syndrome were recruited from six secondary-care
215 reener for myalgic encephalomyelitis/chronic fatigue syndrome) were assessed at baseline and 3 months
216 0.60-2.73; p=0.45) in patients with chronic fatigue syndrome when compared with the general populati
217 y research supports the notion of a discrete fatigue syndrome which can be distinguished from depress
218 patients meeting Oxford criteria for chronic fatigue syndrome who were recruited from six secondary c
219 ticipate that discrete causes of the chronic fatigue syndrome will be found in the future, even if th
220 patients met our strict criteria for chronic fatigue syndrome without co-morbid psychiatric disorder.