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1 s diseases can be reversed or ameliorated by nutritional intervention.
2 20-25% was observed which was refractory to nutritional intervention.
3 d at enrollment and, for cases, after a 5-mo nutritional intervention.
4 bating infection in aged individuals through nutritional intervention.
5 ether pigs and humans respond similarly to a nutritional intervention.
6 IBS-36 questionnaire assessed the impact of nutritional intervention.
7 anabolic signaling that may require targeted nutritional intervention.
8 This process may limit the efficacy of nutritional intervention.
9 to alleviate complex disorders via tailored nutritional intervention.
10 reatment of severe malnutrition in emergency nutritional interventions.
11 tor learning and memory can be reversed with nutritional interventions.
12 eered filtering systems to phytogenetics and nutritional interventions.
13 ta immaturity that is not rescued by current nutritional interventions.
14 ill drive future development of personalized nutritional interventions.
15 tially ameliorated following two widely used nutritional interventions.
16 and detoxifier) can be reversed by targeted nutritional interventions.
17 infections, smoking cessation, and possibly nutritional interventions.
18 isease states and thus could be a target for nutritional interventions.
19 5 and 2015 was performed to identify RCTs of nutritional interventions administered to critically ill
20 evaluation is required to determine whether nutritional interventions and exercise training may pres
23 dogenous lipase activities may be altered by nutritional interventions, and further, that accelerated
24 is possible to reverse these effects through nutritional interventions applied later in development.
25 ematic reviews evaluating dietary intake and nutritional interventions are becoming common but are re
27 clinical and animal studies have identified nutritional intervention as a viable method to curtail t
29 rcent coverage of the same environmental and nutritional interventions, as envisioned by the MDGs, wo
30 nominated friends increased adoption of the nutritional intervention by 12.2% compared with random t
31 stic rationale and experimental evidence for nutritional interventions commonly used in PMDs, includi
33 t their illness and enhance adjustment, or a nutritional intervention, designed to promote a more hea
35 OFC gains in SGA term infants improve after nutritional intervention during the first 9 mo of life a
36 ck of high-quality evidence that proves that nutritional interventions during critical illness reduce
39 utritional treatment may be efficacious as a nutritional intervention for preschoolers aged 2 to 6 ye
42 lth outcomes, and investigating the value of nutritional interventions for mitochondrial disease cond
43 irm the considerable potential for a role of nutritional interventions for osteoarthritis, but they e
44 tophagy/lysosomal system through appropriate nutritional intervention has significant beneficial effe
45 gression, this suggests limited evidence for nutritional interventions having an impact on delaying H
46 Hg (HR, 6.9; 95% CI, 1.5-32.1), and use of a nutritional intervention (HR, 2.3; 95% CI, 1.3-4.1) were
47 uch growth is complex and may be affected by nutritional interventions imposed many years previously.
50 perhaps, in view of the adjunctive nature of nutritional intervention in critical illness, be focused
51 Fetal body composition may be modifiable via nutritional intervention in the mother and thus may play
54 tical challenges reduce the effectiveness of nutritional interventions in complex emergencies, and im
55 lateral sclerosis, and support the study of nutritional interventions in larger randomised controlle
57 timates of delta occur frequently in RCTs of nutritional interventions in the critically ill that are
58 suggest that future research should focus on nutritional interventions in the pre- and postdischarge
60 Combined with other studies of choline and nutritional interventions in this population, this study
63 Findings of controlled trials indicate that nutritional interventions, including vitamin A palmitate
67 gy expenditure and energy intake change, but nutritional intervention is not necessarily beneficial.
68 ve studies and longitudinal studies in which nutritional intervention is provided before cognitive de
71 tochondrial disorders (PMDs), and the use of nutritional interventions is routine in their supportive
72 sensitive period of the life cycle in which nutritional intervention may reap the greatest benefits.
75 ese methods to estimate the causal effect of nutritional interventions on clinical outcomes among cri
76 graphy for evaluating the effect of prenatal nutritional interventions on components of fetal growth.
77 fically answer the question on the impact of nutritional interventions on HIV disease progression and
78 Pediatrics statement on the effects of early nutritional interventions on the development of atopic d
83 art defect risk would help to refine current nutritional intervention strategies to reduce risk and m
87 eviewed the results of randomized controlled nutritional intervention studies that have assessed the
89 ition studies, possible extensions of N-of-1 nutritional intervention studies, and areas of future re
91 articipants of the prospective German Infant Nutritional Intervention study after 10 years of follow-
93 Pancreatic insufficiency was managed with nutritional interventions that included high-calorie die
94 plasma ANGPTL4 concentrations after various nutritional interventions that increase NEFA concentrati
96 ted to result in dietary recommendations and nutritional interventions that optimize individual healt
97 s for randomized controlled trials (RCTs) of nutritional interventions that used mortality as the pri
99 >90 d survival), creating an opportunity for nutritional intervention to stop or reverse cachexia.
102 These results emphasize the need for early nutritional interventions to reduce daily sugar intake i
103 nal pathology, providing a basis for testing nutritional interventions to reduce malaria-associated m
104 dings warrant further studies of therapeutic nutritional interventions to restore arginine metabolism
105 f the abnormal metabolic profile, a targeted nutritional intervention trial with folinic acid, betain
107 ction (PCR), were assessed over 5 years of a nutritional intervention, which promoted adherence to th
109 status after treatment suggest that targeted nutritional intervention with methylcobalamin and folini
110 A set of real samples obtained after human nutritional intervention with placebo or polyphenol-rich
112 a water, sanitation, handwashing (WSH), and nutritional intervention would slow TL attrition during
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