Today's Hours: 10:00am - 6:00pm
Lane Medical Library

Search

Filter Results

Did You Mean:

Search Results

Sort by
relevance
  • Book
    edited by Linda S. Cox.
    Contents:
    Section 1: Background. History of allergen immunotherapy
    Definition of an allergen
    Allergen standardization and manufacturing
    Section 2: Allergic diseases. Allergic respiratory diseases: asthma and allergic rhinitis
    Atopic dermatitis
    Food allergy
    Stinging insects
    Section 3: Mechanisms of allergen immunotherapy. Subcutaneous immunotherapy: aeroallergen
    Sublingual immunotherapy: aeroallergen and venom
    Food tolerance, allergy, and allergen unresponsiveness
    Clinical markers to AIT response
    Biologics for COPD
    Role of biologics in pediatric asthma
    Section 4: Allergen immunotherapy (AIT) and allergen immunomodluatory (AIM) therapies. Breakthroughs in subcutaneous immunotherapy
    Breakthroughs in sublingual immunotherapy
    Food immunotherapy
    Adherence and pharmacoeconomics
    Section 5: AIT and immunomodulatories in investigation. Alternative immunotherapy routes
    Modified allergens: peptides, fragments, and recombinant allergens
    Section 6: Allergen immunomodulatories. Overview of Immunomodulatories
    Anti IGE
    Anti IL5.
    Digital Access ClinicalKey 2020
  • Article
    Barbin GK, Thorley JD, Reinarz JA.
    J Clin Microbiol. 1978 Mar;7(3):286-9.
    Simplified urine microscopy, nitrite testing, and dipstick culture were compared with urine loop streak culture colony counts in 219 random voided specimens to determine the accuracy of the three rapid screening techniques. Nitrite testing resulted in 65% false negative results, which could not be significantly improved by incubation at 37 degrees C but which could be improved by adding nitrate substrate before incubation. Dipstick culture could not be quantitated until after 18 h of incubation. A new, simplified microscopy technique, using unspun, unstained urine, resulted in 4% false negative results and 4% false positive results in specimens containing over 10(5) organisms per ml and was the best method Centrifuges, Gram staining reagents, and counting chambers are not necessary for accurate microscopic screening of random urine specimens for the presence of bacteriuria by this technique, and the results are immediately available.
    Digital Access Access Options