コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 eczema case collection (0-16 year olds with atopic eczema).
2 h atopic eczema and 2,569,030 people without atopic eczema.
3 gests increased fracture risk in people with atopic eczema.
4 month of life was associated with subsequent atopic eczema.
5 ts in adult patients with moderate to severe atopic eczema.
6 suggest that this phototherapy might improve atopic eczema.
7 atecholamine concentrations of patients with atopic eczema.
8 that there is no deficit of linoleic acid in atopic eczema.
9 ere matched to 2,567,872 individuals without atopic eczema.
10 with the most severe or predominantly active atopic eczema.
11 eczema, atopy alone, non-atopic eczema, and atopic eczema.
12 ronger in carriers of fewer risk alleles for atopic eczema.
13 ic asthma, chronic spontaneous urticaria and atopic eczema.
14 is phenotype differs from genetically driven atopic eczema.
15 y and any fracture in those with and without atopic eczema.
16 s and low mood have been linked to offspring atopic eczema.
17 and corticosteroids as treatment options for atopic eczema.
18 treatment of some skin conditions including atopic eczema.
19 ) and related to the odds ratio of infantile atopic eczema.
20 standardization of outcome measurements for atopic eczema.
21 crobiota diversity have been associated with atopic eczema.
22 they have a role in alleviating symptoms of atopic eczema.
23 n CYP27A1 was found to be protective against atopic eczema.
24 t less than 4.5 months increased the risk of atopic eczema.
27 d domestic water has been reported to worsen atopic eczema (AE) and may contribute to its development
34 of BMI and GWG on risk of asthma, wheezing, atopic eczema (AE), and hay fever in children during the
35 SE, and LILACS (1945-2016) for the terms AD, atopic eczema (AE), and multiple other eczematous disord
44 tiple genetic and environmental factors, but atopic eczema also shows great complexity in its heterog
46 ic sensitisation, asthma, allergic rhinitis, atopic eczema and adverse events based on RCT evidence.
49 sent with short stature, immune dysfunction, atopic eczema and gastrointestinal pathology associated
50 ); polygenic risk score for a combination of atopic eczema and general atopic disease had the stronge
51 velopmental contribution to the aetiology of atopic eczema and pointing to potentially modifiable inf
52 oducts was related to a reduced incidence of atopic eczema and rhinoconjunctivitis, but no associatio
54 Many research studies have been published on atopic eczema and these are often summarised in systemat
55 on, uterine leiomyoma, vitamin D deficiency, atopic eczema) and phenotypes defined in the PheWAS Cata
58 systemic monotherapy for moderate-to-severe atopic eczema, and the therapeutic importance of the thi
59 adjunctive treatment for moderate to severe atopic eczema, and the treatment is well tolerated by mo
60 a significant reduction in the incidence of "atopic eczema," "any positive SPT [skin-prick test]," "s
61 diated diseases, such as allergic asthma and atopic eczema, as well as purpose-developed biologics, h
62 es 6 (n = 2956) and 12 (n = 2872) months and atopic eczema ascertained (based on UK Working Party Cri
64 rd methylation of CpG loci within IL-4R with atopic eczema at 12 months (median ratio 1.02, P = .028)
65 ith a slightly reduced relative risk (RR) of atopic eczema at 6 months (adjusted RR, 0.94; 95% CI, 0.
66 sociated with an increased risk of offspring atopic eczema at age 12 months but not at 6 months, robu
67 sociated with an increased risk of infantile atopic eczema at age 12 months, but no significant assoc
69 n the UK Southampton Women Survey, infantile atopic eczema at ages 6 and 12 months was ascertained (m
73 This study aimed to identify subtypes of atopic eczema based on patterns of disease activity thro
74 eyond childhood may reveal clear subtypes of atopic eczema based on patterns of disease activity.
75 ubstantial improvements in the management of atopic eczema, but many patients still suffer a burden o
78 lidate evidence on dietary interventions for atopic eczema/dermatitis (AD) skin symptoms in children
81 ce by age, and among adults reporting active atopic eczema during a given year, only 38% had symptom
84 to generate polygenic risk scores (PRSs) for atopic eczema, general atopic disease, or a combination,
85 atopic eczema subtypes and the infrequent/no atopic eczema group, but only female sex differentiated
87 remain high after childhood, and adult-onset atopic eczema has different risk factor associations tha
88 of azathioprine as systemic monotherapy for atopic eczema has major advantages, which should allow c
90 hazard for all-cause mortality in those with atopic eczema (hazard ratio = 1.04; 99% CI = 1.03-1.06),
91 gh many risk factors have been described for atopic eczema in children, little is known about the ecz
92 ial of water softeners for the prevention of atopic eczema in high-risk infants is feasible and accep
93 ations were identified with hypertension and atopic eczema in models accounting for age, sex, and eth
94 ne the relation of maternal stress/mood with atopic eczema in the offspring, focusing particularly on
97 genetic mutations previously associated with atopic eczema, including filaggrin-null mutations, and a
103 Any link could have substantial effect; atopic eczema is common, and fractures have associated m
107 on-and also a strong genetic risk factor for atopic eczema, marked a significant breakthrough in the
108 ics), including adults (>=18 years old) with atopic eczema matched (by age, sex, general practice, an
113 sex, and ethnicity, and the association with atopic eczema (odds ratio [OR], 1.68; 95% CI, 1.36-2.07;
115 sition may play a role in the development of atopic eczema or atopic sensitization in breastfed infan
117 7-44.54] and 13.97 [95% CI, 7.33-26.4]), and atopic eczema (OR, 9.39 [95% CI, 4.9-19.3] and 9.5 [95%
118 czema trials, to define quality criteria for atopic eczema outcome measures and to prioritize topics
124 czema were identified based on self-reported atopic eczema period prevalence at multiple occasions.
126 cores were used to investigate the effect of atopic eczema-related risk alleles on this association.
130 ancy and infancy with questionnaire-reported atopic eczema, rhinoconjunctivitis, and asthma in 40,614
131 of probiotic milk products protects against atopic eczema, rhinoconjunctivitis, and asthma in early
133 linking maternal stress at preconception to atopic eczema risk, supporting a developmental contribut
134 t patients with a mean (SD) patient Recap of Atopic Eczema score of 11.7 (7.2), mean (SD) patient age
138 erstood that primary skin disorders, such as atopic eczema, skin dryness, psoriasis, and urticaria, c
139 feeding, predicted differences between the 3 atopic eczema subtypes and the infrequent/no atopic ecze
140 outcome was the age period of self-reported atopic eczema symptom onset based on repeated measures o
142 ermine the proportion of subjects who report atopic eczema symptoms between birth and midadulthood an
143 assessed the effect of these risk factors on atopic eczema symptoms using mixed-effect logistic regre
144 y relevant improvement in moderate-to-severe atopic eczema that remains active despite optimum therap
146 ss and MCID of four outcome measures used in atopic eczema: the Severity Scoring of Atopic Dermatitis
147 ture of trials of calcineurin inhibitors for atopic eczema to document the extent to which comparison
148 response to skin stress in diseases such as atopic eczema, to various agents such as retinoic acid,
149 otal of 174 randomized controlled trials for atopic eczema treatments were identified in which pimecr
150 d inadequately validated outcome measures in atopic eczema trials is a major obstacle to practising e
151 ustry) to determine core outcome domains for atopic eczema trials, to define quality criteria for ato
154 ial (children 1-5 years with moderate-severe atopic eczema); UK BEEP trial (2 year olds at high risk
155 rial (2 year olds at high risk of developing atopic eczema); UK-Irish eczema case collection (0-16 ye
158 cant association between post-natal mood and atopic eczema was seen after taking account of preconcep
159 3.71; P = .05), whereas the association with atopic eczema was significant in White participants (OR,
160 We aimed to determine whether adults with atopic eczema were at increased risk of death overall an
163 d, milk, and adipose tissue of patients with atopic eczema, whereas concentrations of linoleic acid m
165 tent class analysis identified 4 subtypes of atopic eczema with distinct patterns of disease activity