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 tions were proposed (eg food allergy, atopic dermatitis).
2 for future prevention or treatment of atopic dermatitis.
3 tion such as psoriasis and contact or atopic dermatitis.
4 m development and subsequent risk for atopic dermatitis.
5 howed no evidence of association with atopic dermatitis.
6 ts and adults with moderate-to-severe atopic dermatitis.
7 is associated with reduced asthma and atopic dermatitis.
8 published datasets from subjects with atopic dermatitis.
9 females was associated with more seborrheic dermatitis.
10 evoked scratching in a mouse model of atopic dermatitis.
11 mouse model of IL-22-induced psoriasis-like dermatitis.
12 included, of whom 636 (14.5%) had seborrheic dermatitis.
13 factors were not associated with seborrheic dermatitis.
14 lesion formation and intense itch in atopic dermatitis.
15 ema area and severity index (EASI) in atopic dermatitis.
16 ics in adults with moderate to severe atopic dermatitis.
17 and long-term effect in children with atopic dermatitis.
18 a mouse model of IL-23 mediated psoriasiform dermatitis.
19 ough MRGPRB2 drives itch in allergic contact dermatitis.
20 of these NPs in a model of allergic contact dermatitis.
21 that enter the skin and cause itch in atopic dermatitis.
22 dant capacity are associated with seborrheic dermatitis.
23 nagement of asthma, food allergy, and atopic dermatitis.
24 ls are downregulated in patients with atopic dermatitis.
25 nfection to occur in association with atopic dermatitis.
26 eterious effects of PAR2 in models of atopic dermatitis.
27 b in patients with moderate to severe atopic dermatitis.
28 l profile changes that result in response to dermatitis.
29 sent similar characteristics, such as atopic dermatitis.
30 ts and adults with moderate-to-severe atopic dermatitis.
31 identify new strategies for targeting atopic dermatitis.
32 approach for antipruritic therapy in atopic dermatitis.
33 philic esophagitis, food allergy, and atopic dermatitis.
34 he development of WD-associated psoriasiform dermatitis.
35 on is a feature of skin aging and eczematous dermatitis.
36 d by donor monocytes to generate a GVHD-like dermatitis.
37 nd related phenols, which can induce contact dermatitis.
38 the innate immune system in allergic contact dermatitis (ACD) has traditionally been confined to the
39 tiple preclinical models of allergic contact dermatitis (ACD), a pruritic inflammatory skin disorder,
44 and in the placebo plus erlotinib group were dermatitis acneiform (20 [9%]) and increased alanine ami
45 re hypertension (52 [24%]; grade 3 only) and dermatitis acneiform (33 [15%]), and in the placebo plus
46 e-limiting toxicities (grade 2 hypertension, dermatitis acneiform, and memory impairment in patient 1
47 EKTI exonic mutations associated with atopic dermatitis (AD) affect the protease inhibitory activity
50 lk allergy, and/or moderate to severe atopic dermatitis (AD) and a positive egg/milk skin prick test
52 ed in the pathophysiology of not only atopic dermatitis (AD) and psoriasis (PSO) but also lupus eryth
59 racial/ethnic differences in incident atopic dermatitis (AD) in childhood, few studies have examined
60 Farm exposures may reduce the risk of atopic dermatitis (AD) in children, but this is controversial a
70 t research advancements indicate that atopic dermatitis (AD) is a complex disease characterized by di
89 assessed molecular changes in chronic atopic dermatitis (AD) lesions, little is known about the trans
98 , allergic conjunctivitis (AC), and allergic dermatitis (AD) were defined from self-completed questio
101 The nonlesional skin of children with atopic dermatitis (AD) with peanut allergy (PA) is associated w
102 3A, KIF3A, have been associated with atopic dermatitis (AD), a chronic inflammatory skin disorder.
103 years) for the assessment of current atopic dermatitis (AD), allergic rhinitis (AR), asthma and sens
104 ng, who is best known for his work in atopic dermatitis (AD), along with many other contributions in
105 adults and young children with early atopic dermatitis (AD), but chronologic changes in the blood of
106 health care utilization for pediatric atopic dermatitis (AD), but do not account for disease severity
107 ed risk factor for the development of atopic dermatitis (AD), but several aspects of this association
108 pathogenic cytokine in patients with atopic dermatitis (AD), but the molecular effects of IL-22 anta
110 ronic inflammatory conditions such as atopic dermatitis (AD), chronic obstructive pulmonary disease (
111 e the effect of cheese consumption on atopic dermatitis (AD), food allergy (FA), allergic rhinitis, a
112 tice guideline "systemic treatment of atopic dermatitis (AD)," we critically appraised evidence on sy
131 bsence of common allergic conditions (atopic dermatitis [AD], IgE-mediated food allergy [IgE-FA], ast
133 biopsies promote our understanding of atopic dermatitis/AD pathomechanisms in infants/toddlers with e
136 ergen and aeroallergen sensitization, atopic dermatitis, allergic rhinitis, asthma, and challenge-pro
138 (e.g., Dexamethasone) an induced skin atopic dermatitis, an induced psoriasis-like inflammation, a ho
139 as little as 4 weeks with a WD promoted mild dermatitis and accumulation of IL-17A-producing gammadel
147 ession of VCAM1 is upregulated in spongiotic dermatitis and lupus and is associated with a dense peri
150 minated skin inflammation that mimics atopic dermatitis and sensitizes the airways for antigen challe
152 stratum corneum (SC) of patients with atopic dermatitis and their impaired skin barrier and water-hol
154 ze, urticaria, rhinitis and visible flexural dermatitis), and effect modification by Sm exposure.
155 skin diseases, including ichthyosis, atopic dermatitis, and a multitude of clinical eczema variants.
156 aneous diseases (including psoriasis, atopic dermatitis, and alopecia areata) and eight other immune-
159 is approved for treatment of asthma, atopic dermatitis, and chronic sinusitis with nasal polyposis.
161 rom diseases as diverse as psoriasis, atopic dermatitis, and erythrokeratodermia variabilis, suggesti
162 atology clinical trials in psoriasis, atopic dermatitis, and hidradenitis have been suspended, termin
164 g that is used to treat psoriasis and atopic dermatitis, and is thought to function through regulatio
165 with a particular focus on asthma and atopic dermatitis, and provide insights into the roles of these
171 s, including asthma, food allergy and atopic dermatitis, are increasing in prevalence, particularly i
174 tors for adult allergic rhinitis were atopic dermatitis, asthma and asymptomatic sensitization to pol
175 factor for allergic diseases such as atopic dermatitis, asthma, allergic rhinitis, food allergy, con
176 c and inflammatory disorders, such as atopic dermatitis, asthma, rheumatoid arthritis, colitis, and c
180 e history: He has been suffering from atopic dermatitis, bronchial asthma, and food allergies since c
181 These polymorphisms associate with atopic dermatitis but how they affect Ca2+ signalling and cell
182 the association between C-section and atopic dermatitis by age four and examine potential sources of
185 ften suffering from an IgE-mediated allergic dermatitis caused by bites of midges (Culicoides spp).
187 salinity persisting weeks to months, and (2) dermatitis characterized grossly by patchy skin pallor t
188 r cofactor in atopic diseases such as atopic dermatitis, chronic rhinosinusitis with nasal polyps, an
189 logicals for the treatment of asthma, atopic dermatitis, chronic rhinosinusitis with nasal polyps, or
190 2%), grade 2; and 1 (0.5%) grade 3 radiation dermatitis (Common Terminology Criteria for Adverse Even
191 ation is ~50% higher in children with atopic dermatitis compared to children from a high-risk allergy
193 mice characterized by chronic proliferative dermatitis (cpdm), which is propagated by TNFR1-induced
194 ugh 3 years of age for development of atopic dermatitis; data on allergic sensitization and asthma we
195 iction tasks from ulcerative colitis, atopic dermatitis, diabetes, to many cancer subtypes for a tota
196 n a young girl being treated for both atopic dermatitis, diagnosed at 1 year of age, and bronchial as
197 diagnosed the patient with allergic contact dermatitis due to the EITC and BITC present in nitrile r
198 increase the risk of food allergy and atopic dermatitis/eczema but may prevent peanut and egg allergy
201 or of transcription 3 (STAT3) mutations have dermatitis, enhanced IgE production despite a relative l
202 are predisposed to mount an allergic contact dermatitis, especially at hapten threshold levels elicit
203 Guidelines on the use of dupilumab in atopic dermatitis follow the GRADE approach in formulating reco
204 link between skin barrier impairment, atopic dermatitis, food allergy, allergic asthma, and allergic
205 t- and food-allergic sensitization or atopic dermatitis had higher circulating memory Treg cells, but
206 r some chronic itch disorders such as atopic dermatitis has given widespread recognition to the impor
207 c rhinitis, asthma, food allergy, and atopic dermatitis has increased dramatically during the last de
208 reliable biomarkers in psoriasis and atopic dermatitis has lagged behind therapeutic progress, we cr
209 Research into the pathogenesis of atopic dermatitis has led to the testing and development of num
210 matory diseases, including asthma and atopic dermatitis, has established the need for effective IL-33
212 cosal inflammatory disorders, such as atopic dermatitis, have been associated with an impaired epithe
214 II deficiency, TG2 in celiac disease, TG3 in dermatitis herpetiformis, TG4 in autoimmume polyglandula
218 ered that MrgprA3(+) neurons respond to skin dermatitis in a way that is unique from other sensory ne
220 required for the development of psoriasiform dermatitis in an IL-23 intradermal injection model.
221 versus ever being fed human milk and atopic dermatitis in childhood or 2) the duration of any human
223 = .001), a 17% greater risk of ever allergic dermatitis in children (OR, 1.17; 95% CI, 1.04-1.32; P =
226 34% greater risk of ever or current allergic dermatitis in infants up to 2 years of age (OR, 1.34; 95
227 (cpdm) , where cpdm = chronic proliferative dermatitis in mice) with and without melanoma tumor allo
228 y were to determine the prevalence of atopic dermatitis in the population of the United States, the d
232 cted in the skin in steady-state, psoriasis, dermatitis, infection, and malignant skin diseases.
234 he individual diseases, children with atopic dermatitis, inhalant-, and food-allergic sensitization h
235 d >=12 years) with moderate-to-severe atopic dermatitis (Investigator Global Assessment score >=3, Ec
244 matitis, the Patient-Oriented Scoring Atopic Dermatitis-itch, the Patient-Oriented Scoring Atopic Der
246 ore food allergen sensitization on an atopic dermatitis-like skin lesion, followed by intragastric al
253 ients with CP of inflammatory origin (atopic dermatitis), neuropathic origin (brachioradial pruritus)
255 lated ACD and 7 hairdressers without contact dermatitis on day 4 after patch testing with 1% PPD in p
260 the association between C-section and atopic dermatitis overall and when stratified by demographic an
261 l disease (IBD) (P = 1.17 x 10-4) and eczema/dermatitis (P = 2.81 x 10-3), as well as associations be
262 ly shown that caspase-1 and -11 promoted the dermatitis pathology of cpdm mice and mediated cell deat
266 igh vitiligo, high psoriasis, and low atopic dermatitis polygenic risk scores (PRSs) were associated
269 atment models of oxazolone- and DNFB-induced dermatitis, PZ-235 significantly attenuated skin thicken
270 showed modest efficacy and decreased atopic dermatitis-related biomarkers in moderate to severe atop
274 was evidence that C-section increased atopic dermatitis risk among certain subgroups (eg firstborns,
275 ive association between C-section and atopic dermatitis [RR(95%CI): 1.06(1.03, 1.10)], this effect wa
277 is-itch, the Patient-Oriented Scoring Atopic Dermatitis-sleep, and the Numerical Rating Scale of pain
278 TMEM79 is a predisposition gene for Atopic dermatitis, suggesting deregulation of Wnt/FZD signaling
279 atified approach to the management of atopic dermatitis, supporting the use of targeted treatments wi
280 ntibody (dupilumab) on two cases with atopic dermatitis that was refractory to conventional managemen
281 rophils are key initiators of itch in atopic dermatitis, the most prevalent chronic itch disorder.
282 Measure, the Patient-Oriented Scoring Atopic Dermatitis, the Patient-Oriented Scoring Atopic Dermatit
289 sociated with anxiety and depression, atopic dermatitis was associated with suicidal ideation, and th
292 om patients with DOCK8 deficiency and atopic dermatitis were profiled on a cytokine/chemokine panel f
293 t intake was associated with less seborrheic dermatitis, whereas high adherence to a "Western" dietar
294 biopsies from patients and mice with atopic dermatitis, whereas their inhibition attenuated scratchi
295 levels are increased in patients with atopic dermatitis, which commonly precedes asthma in the atopic
296 KLK6 causes generalized, severe psoriasiform dermatitis with spontaneous development of debilitating
297 lion adults would have a diagnosis of atopic dermatitis, with 6.6 million meeting criteria for modera
299 in barrier and prevention or treating atopic dermatitis would have beneficial effects on prevention o
300 olybacterial bovine wound infection 'digital dermatitis', Zn/Cu-shellac adhered rapidly and robustly