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Deciphering the complexities of atopic dermatitis: Shifting paradigms in treatment approaches
Deciphering the complexities of atopic dermatitis: Shifting paradigms in treatment approaches
Mechanisms of abnormal lamellar body secretion and the dysfunctional skin barrier in patients with atopic dermatitis
Causes of epidermal filaggrin reduction and their role in the pathogenesis of atopic dermatitis
The Harmonising Outcome Measures for Eczema (HOME) statement to assess clinical signs of atopic eczema in trials
Peeling off the genetics of atopic dermatitis–like congenital disorders
Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis prevention
Application of moisturizer to neonates prevents development of atopic dermatitis
Randomized trial of vitamin D supplementation for winter-related atopic dermatitis in children
MicroRNA-146a alleviates chronic skin inflammation in atopic dermatitis through suppression of innate immune responses in keratinocytes
Identification of novel gene signatures in patients with atopic dermatitis complicated by eczema herpeticum
Distinct behavior of human Langerhans cells and inflammatory dendritic epidermal cells at tight junctions in patients with atopic dermatitis
Eczematous sensitization, a novel pathway for allergic sensitization, can occur in an early stage of eczema
Peanut allergy: Effect of environmental peanut exposure in children with filaggrin loss-of-function mutations
Filaggrin loss-of-function mutations are associated with food allergy in childhood and adolescence
Aspirin desensitization in patients with aspirin-induced and aspirin-tolerant asthma: A double-blind study
Epistasis between serine protease inhibitor Kazal-type 5 ( SPINK5 ) and thymic stromal lymphopoietin ( TSLP ) genes contributes to childhood asthma
Assessing the validity of the RAND Negative Impact of Asthma on Quality of Life Short Forms
Economic and health effect of full adherence to controller therapy in adults with uncontrolled asthma: A simulation study
Value of simulation studies to assess health policies
Lung function trajectories from birth through puberty reflect asthma phenotypes with allergic comorbidity
Asthma and lung development: Another piece in the jigsaw, but the full picture has yet to emerge
Expression of 11β-hydroxysteroid dehydrogenase 1 and 2 in patients with chronic rhinosinusitis and their possible contribution to local glucocorticoid activation in sinus mucosa
Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency
Tolerogenic signaling by pulmonary CD1c+ dendritic cells induces regulatory T cells in patients with chronic obstructive pulmonary disease by IL-27/IL-10/inducible costimulator ligand
Residual genomic profile after cyclosporine treatment may offer insights into atopic dermatitis reoccurrence
Proteome analysis of stratum corneum from atopic dermatitis patients by hybrid quadrupole-orbitrap mass spectrometer
Trends in hospitalizations for food-induced anaphylaxis in US children, 2000-2009
Exposure to parental smoking in childhood is associated with persistence of respiratory symptoms into young adult life
Comparing safety of abrasion and tape-stripping as skin preparation in allergen-specific epicutaneous immunotherapy
IgE antibodies to mountain cedar pollen predominantly recognize multiple conformational epitopes on Jun a 1
Systemic and localized seminal plasma hypersensitivity patients exhibit divergent immunologic characteristics
Genome-wide expression profiling of B lymphocytes reveals IL4R increase in allergic asthma
TNF-α/IL-17 synergy inhibits IL-13 bioactivity via IL-13Rα2 induction
Basophils increase in Crohn disease and ulcerative colitis and favor mesenteric lymph node memory TH17/TH1 response
Induction of remission of idiopathic anaphylaxis with rituximab
Lessons in gene hunting: A RAG1 mutation presenting with agammaglobulinemia and absence of B cells
IgE allergen component-based profiling and atopic manifestations in patients with Netherton syndrome
Invariant natural killer T cells in patients with common variable immunodeficiency
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