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1 pared with another intervention or a vehicle/emollient.
2 ents in the control arm were asked to use no emollients.
3 example, fragrances and other ingredients in emollients.
4 or tacrolimus ointment than for steroids and emollients.
5  without the requirement to constantly apply emollients.
6 ty of various topical agents, and the use of emollients.
7            All children and parents received emollient and patient education about AD and basic skin
8        Topically applied formulations (e.g., emollients and moisturizers) may influence the optical p
9  by wearing impermeable gloves) and applying emollients and potent topical glucocorticoids.
10 ally higher in children with frequent use of emollients compared to uncommon users, reaching statisti
11 show that applying a thin layer of glycerine emollient containing nanoparticles of either calcium car
12 ionate, clobetasol propionate, and a vehicle/emollient control.
13                       Patients cited topical emollients, corticosteroids, and salicylic acid along wi
14 stamines, topical corticosteroids, and thick emollient creams, rendering their eruption tolerable for
15  measures such as the application of topical emollients have shown mixed results in the prevention of
16                                      Topical emollients improved neonatal skin condition, but were as
17 sise the evidence for topical application of emollients in the prevention of invasive infection and m
18                                      Topical emollients might improve skin integrity and barrier func
19 ffect of prophylactic application of topical emollient (ointments, creams, or oils) on the incidence
20 ctive effect was found with the use of daily emollient on the cumulative incidence of atopic dermatit
21 conceivable to design resveratrol-containing emollient or patch, as well as sunscreen and skin-care p
22 ial data do not provide strong evidence that emollients prevent invasive infection or death in preter
23                                There were no emollient-related adverse events and no differences in a
24 cidence of infection in infants treated with emollient (relative risk 1.20, 95% CI 1.01-1.42), but no
25 s explained by increased use of the specific emollients that are used to treat pruritic and inflamed
26 ntion arm were instructed to apply full-body emollient therapy at least once per day starting within
27   The results of this trial demonstrate that emollient therapy from birth represents a feasible, safe
28               If confirmed in larger trials, emollient therapy from birth would be a simple and low-c
29  to ascertain whether topical application of emollients to enhance skin barrier function would preven
30                                              Emollient use and atopic dermatitis were associated with
31          To evaluate the association between emollient use, atopic dermatitis and FLG mutations, resp
32  a vapor-permeable membrane (Gore-Tex) or an emollient (Vaseline), applied after acute barrier disrup
33 formation about atopic dermatitis and use of emollients was obtained from questionnaires completed by

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