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1 ebo group, and included headache, fever, and malaise).
2 /soreness, chills, arthralgia, anorexia, and malaise).
3 ng properties of LiCl or by a lesion-induced malaise.
4 ors, arthralgias, myalgias, headache, and/or malaise.
5 l tastant and toxin-induced gastrointestinal malaise.
6 s, after having experienced gastrointestinal malaise.
7 t presenting with complaints of headache and malaise.
8 also a harbinger of cellular and organismal malaise.
9 ssociated with grade I flu-like symptoms and malaise.
10 average meal size and independent of nausea/malaise.
11 ic effect of NAc core GLP-1 is not caused by malaise.
12 he taste that was previously associated with malaise.
13 he taste that was previously associated with malaise.
14 components of anxiety, stress, and visceral malaise.
15 avoidance of tastes associated with visceral malaise.
16 toxicity, nausea or vomiting, and fatigue or malaise.
17 nia, hyponatremia, hypokalemia, fatigue, and malaise.
18 lulike" illness associated with myalgias and malaise.
19 body weight gain without causing CNS-related malaise.
20 did not confirm that SEB challenge promotes malaise.
21 nes were well-tolerated, with myalgia (19%), malaise (14%), and local pain (10%) the most frequent ad
23 geal signs but less frequently complained of malaise; (2) had larger EM skin lesions despite similar
24 eveloped low-grade fever, chills, cough, and malaise 3 days prior to admission, and then progressive
25 (59.7%), headache (46.8%), fatigue (44.2%), malaise (39%), paresthesias (32.5%), peripheral facial p
26 ents treated with vorinostat were fatigue or malaise (51 [16%] patients in the vorinostat group vs 25
27 cific manifestations, including fever (96%), malaise (88%), myalgia (57%), cough (25%), and dizziness
28 ed to this hospital because of confusion and malaise after resection of a papillary urothelial cancer
30 xicity, including fever, chills, nausea, and malaise, although no patient had grade 3 or 4 toxicity.
33 ic mechanism through which cisplatin-induced malaise and energy balance dysregulation are mediated.
35 n VRC 319 and 36 [80%] of 45 in VRC 320) and malaise and headache were the most frequent systemic sym
40 V) developed signs of acute viral infection (malaise and weight loss) and had MCMV loads that were re
41 patient presented with shortness of breath, malaise, and cough that had developed 3 days prior to ad
48 entations with enlarged lymph nodes, fevers, malaise, anorexia, weight loss, hypoalbuminemia, and gas
51 s (CB) have been used to combat the visceral malaise associated with chronic disease, although the me
53 ement of the Environment scores and parental malaise attenuated associations with the mother's IQ but
54 sing a small number of RBC units for general malaise attributed to anaemia, a practice that appears t
55 using small numbers of RBC units for general malaise attributed to anaemia, a practice which appears
56 a neuromodulator in the hindbrain to produce malaise by potentiating visceral afferent signaling at t
57 een associated with lithium chloride-induced malaise, c-Fos protein expression increased dramatically
58 erent families cause a syndrome of fever and malaise, 'capillary leak' with loss of plasma volume, an
60 the first dose and typically included fever, malaise, cough, dyspnea, and interstitial pneumonitis.
61 nfusion, there was resolution of fatigue and malaise, disappearance of fever, and regression of lymph
62 e symptoms (such as fever, chills, headache, malaise, fatigue, arthralgias, and myalgias) before rand
64 3 or 4 treatment-related adverse events were malaise/fatigue and diarrhea, occurring in 17% and 7% of
65 es were anemia, leukopenia/granulocytopenia, malaise/fatigue, nausea/vomiting, alopecia, thrombocytop
66 her common but mild adverse effects included malaise/fatigue, peripheral edema, and hyperglycemia.
68 for many symptoms such as sleep disorder and malaise/feebleness was also significantly improved after
70 ffectiveness of cannabinoids in blocking the malaise generated by TNF-releasing disease processes by
71 loin pain, diarrhoea, and vomiting; one had malaise, headache, and chest pain; and one had severe ch
73 fluconazole discontinued treatment owing to malaise, headache, and moderate dizziness (Common Termin
74 ing fever in 23 (82%), headache in 14 (50%), malaise in 13 (46%), dizziness in nine (32%), myalgia in
75 ated distinct mechanisms for post-exertional malaise in CFS and START and STOPP phenotypes of GWI.
76 Marek's disease virus (MDV) causes a general malaise in chickens that is mostly characterized by the
77 -induced pica (a proxy for nausea/behavioral malaise in nonvomiting laboratory rodents) and that CeA
78 tested in rats with 2 measures sensitive to malaise, increased kaolin consumption (pica behavior) an
83 e general health questionnaire (GHQ) and the malaise inventory (divided into psychological and somati
84 or the psychological symptom subscale of the malaise inventory (regression coefficient -0.024, 95 per
86 ured using the Psychological subscale of the Malaise Inventory; frequency of physical activity, by qu
87 including fever (>/=38.5 degrees C), rigors, malaise, lethargy, flank pain, hematuria, suprapubic dis
91 ia and constitutional symptoms consisting of malaise, myalgias, and anorexia were the dose-limiting t
93 nted with 6 days of sinus congestion, fever, malaise, myalgias, episcleritis, and a morbilliform rash
95 %] of 171), headache (12 [7.0%] of 171), and malaise (nine [5.3%] of 171) in patients receiving ledip
98 ctions in meal size and is not due to nausea/malaise or prolonged suppression of locomotor activity.
99 These effects did not appear to be due to malaise or suppression of motor behavior because drug-tr
101 de 3), and a composite of asthenia, fatigue, malaise, or lethargy (56% with any grade, 9% with grade
102 Refractory giardiasis was associated with malaise (P = .007) and anorexia (P = .02), with previous
103 (extremity paresthesia, arthralgia, myalgia, malaise, pruritus, headache, dizziness, metallic taste,
105 tioned stimulus [CS]) with the experience of malaise (such as that induced by LiCl; unconditioned sti
110 n, he developed recurrent rashes with fever, malaise, weakness, hepatitis, weight loss, and renal fai
112 cantly decreased food intake without causing malaise, whereas intracerebroventricular infusion of apo
113 ns and symptoms such as headache, fever, and malaise, which can progress to chronic airway inflammati
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