Immunodeficiencies: Significance for Gastrointestinal Disease
Viral Gastroenteritis, Page: 47-71
2016
- 6Citations
- 12Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Book Chapter Description
Primary immunodeficiency diseases (PIDs) represent a heterogeneous group of genetically determined disorders that influence the development and function of different components of adaptive and innate immunity. PIDs include antibody deficiencies (IgA deficiency, common variable immunodeficiency, X-linked agammaglobulinemia, and the hyper IgM syndrome) and combined B-cell and T-cell deficiencies, the most serious form being severe combined immunodeficiency (SCID). In the chapter, a summary of the gastrointestinal infections of viral origin, associated with the most common forms of PIDs is presented. The risk of infection by live polio and rotavirus vaccine strains and the importance of early diagnosis of PID in the context of oral vaccination is assessed.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/B9780128022412000031; http://dx.doi.org/10.1016/b978-0-12-802241-2.00003-1; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84987825017&origin=inward; http://linkinghub.elsevier.com/retrieve/pii/B9780128022412000031; http://api.elsevier.com/content/article/PII:B9780128022412000031?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:B9780128022412000031?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/B9780128022412000031; https://dx.doi.org/10.1016/b978-0-12-802241-2.00003-1
Elsevier BV
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