Welcome to CDC Stacks | A Potential Cellular Explanation for the Increased Risk of Clostridium difficile Infection Due to Hypoalbuminemia: A Response to Di Bella SD et al - 36222 | CDC Public Access
Stacks Logo
Advanced Search
Select up to three search categories and corresponding keywords using the fields to the right. Refer to the Help section for more detailed instructions.
 
 
Help
Clear All Simple Search
Advanced Search
A Potential Cellular Explanation for the Increased Risk of Clostridium difficile Infection Due to Hypoalbuminemia: A Response to Di Bella SD et al
  • Published Date:
    Oct 12 2015
  • Source:
    Infect Control Hosp Epidemiol. 36(12):1480.
Filetype[PDF - 29.18 KB]


Details:
No Related Documents.
You May Also Like:
  1. A Simulation-Based Assessment of Strategies to Control Clostridium Difficile Transmission and Infection
    Personal Author:
    Rubin, Michael A.; Jones, Makoto; Leecaster, Molly; Khader, Karim; Ray, Willy; Huttner, Angela; Huttner, Benedikt; Toth, Damon; Sablay, Theodore; Borotkanics, Robert J.; Gerding, Dale N.; Samore, Matthew H.;
    Published:
    Nov 21 2013
    Source:
    PLoS One. 2013; 8(11).
    Description:
    Background : Clostridium difficile is one of the most common and important nosocomial pathogens, causing severe gastrointestinal disease in hospitalized patients. Although "bundled" interventions have been proposed and promoted, optimal control strat...
    File Type:
    Filetype[PDF - 765.01 KB]
  2. Identification of Population at Risk for Future Clostridium difficile Infection Following Hospital Discharge to be Targeted for Vaccine Trials
    Personal Author:
    Baggs, James; Yousey-Hindes, Kimberly; Ashley, Elizabeth Dodds; Meek, James; Dumyati, Ghinwa; Cohen, Jessica; Wise, Matthew E.; McDonald, L. Clifford; Lessa, Fernanda C.;
    Published:
    Oct 9 2015
    Source:
    Vaccine. 33(46):6241-6249.
    Description:
    Background : Efforts to develop a Clostridium difficile vaccine are underway; identification of patients at risk for C. difficile infection (CDI) is critical to inform vaccine trials. We identified groups at high risk of CDI ≥28 days after hospital...
    File Type:
    Filetype[PDF - 636.97 KB]
  3. Increased MDSC Accumulation and Th2 Biased Response to Influenza A Virus Infection in the Absence of TLR7 in Mice
    Personal Author:
    Jeisy-Scott, Victoria; Davis, William G.; Patel, Jenish R.; Bowzard, John Bradford; Shieh, Wun-Ju; Zaki, Sherif R.; Katz, Jacqueline M.; Sambhara, Suryaprakash;
    Published:
    Sep 23 2011
    Source:
    PLoS One. 2011; 6(9).
    Description:
    Toll-like receptors (TLRs) play an important role in the induction of innate and adaptive immune response against influenza A virus (IAV) infection; however, the role of Toll-like receptor 7 (TLR7) during the innate immune response to IAV infection a...
    File Type:
    Filetype[PDF - 980.12 KB]
  4. Screening Blood Donors at Risk for Malaria: Reply to Hänscheid et al.
    Personal Author:
    Benito, A.; Rubio, J.M.;
    Published:
    Aug 2002
    Source:
    Emerg Infect Dis. 8(8):873-874.
    File Type:
    Filetype[PDF - 165.13 KB]
  5. A novel approach to generate a recombinant toxoid vaccine against Clostridium difficile
    Personal Author:
    Donald, Robert G. K.; Flint, Mike; Kalyan, Narender; Johnson, Erik; Witko, Susan E.; Kotash, Cheryl; Zhao, Ping; Megati, Shakuntala; Yurgelonis, Irina; Lee, Phillip Kwok; Matsuka, Yury V.; Severina, Elena; Deatly, Anne; Sidhu, Mini; Jansen, Kathrin U.; Minton, Nigel P.; Anderson, Annaliesa S.;
    Published:
    Apr 29 2013
    Source:
    Microbiology. 159(Pt 7):1254-1266.
    Description:
    The Clostridium difficile toxins A and B are primarily responsible for symptoms of C. difficile associated disease and are prime targets for vaccine development. We describe a plasmid-based system for the production of genetically modified toxins in ...
    File Type:
    Filetype[PDF - 880.10 KB]