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Therapy of autoinflammatory syndromes
Therapy of autoinflammatory syndromes
Autoinflammation: The prominent role of IL-1 in monogenic autoinflammatory diseases and implications for common illnesses
Autoinflammation: The prominent role of IL-1 in monogenic autoinflammatory diseases and implications for common illnesses
Improving cellular therapy for primary immune deficiency diseases: Recognition, diagnosis, and management
Primary immunodeficiencies: 2009 update
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Thirteen-year follow-up of early intervention with an inhaled corticosteroid in patients with asthma
New-onset mild asthma III: A sequel to 2 “Oscar winners”
Adrenergic β2-receptor genotype predisposes to exacerbations in steroid-treated asthmatic patients taking frequent albuterol or salmeterol
Pharmacogenetics of β2-agonists in children
Dispensing of fluticasone propionate/salmeterol combination in the summer and asthma-related outcomes in the fall
Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility
Omalizumab for the treatment of exacerbations in children with inadequately controlled allergic (IgE-mediated) asthma
Prolonged bronchoprotection against inhaled methacholine by inhaled BI 1744, a long-acting β2-agonist, in patients with mild asthma
The glutathione-S-transferase Mu 1 null genotype modulates ozone-induced airway inflammation in human subjects
High doses of inhaled corticosteroids during the first trimester of pregnancy and congenital malformations
Broad defects in epidermal cornification in atopic dermatitis identified through genomic analysis
Familial atypical cold urticaria: Description of a new hereditary disease
Global variations in prevalence of eczema symptoms in children from ISAAC Phase Three
Hypersensitivity reactions to mAbs: 105 desensitizations in 23 patients, from evaluation to treatment
Epinephrine treatment is infrequent and biphasic reactions are rare in food-induced reactions during oral food challenges in children
Assessment of component-resolved in vitro diagnosis of celeriac allergy
Assessment of psychological distress among children and adolescents with food allergy
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
Novel pathogenic mechanism and therapeutic approaches to angioedema associated with C1 inhibitor deficiency
ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia
Correction
Hypereosinophilic syndrome: A multicenter, retrospective analysis of clinical characteristics and response to therapy
Eosinophilic gastrointestinal disease and peanut allergy are alternatively associated with IL-5+ and IL-5− TH2 responses
Selective control of SIRP-α–positive airway dendritic cell trafficking through CD47 is critical for the development of TH2-mediated allergic inflammation
Antigen-driven basophil activation is indicative of early Necator americanus infection in IgE-seronegative patients
Adverse reactions during peanut oral immunotherapy home dosing
Pilot study of budesonide inhalant suspension irrigations for chronic eosinophilic sinusitis
Quoting a landmark paper on the beneficial effects of probiotics
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency
Placental transfer of allergen-specific IgG but not IgE from a specific immunotherapy–treated mother
Increased IFN-γ activity in seasonal allergic rhinitis is decreased by corticosteroid treatment
Diagnosis of primary immunodeficiency: Let your eyes do the talking
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Footnotes1
CME Activities Calendar: American Academy of Allergy Asthma & Immunology