Bilirubin metabolism and congenital jaundice
Hospital Practice, ISSN: 8750-2836, Vol: 20, Issue: 2, Page: 83-106
1985
- 5Citations
- 5Captures
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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.
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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.
Review Description
Although hyperbilirubinemia per se rarely results in secondary tissue damage, it is of considerable clinical interest as a manifestation of a variety of inherited and acquired disease processes. New findings and evolving concepts are discssed in the context of the various clinical disorders of bilirubin metabolism.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0021849764&origin=inward; http://dx.doi.org/10.1080/21548331.1985.11702995; http://www.ncbi.nlm.nih.gov/pubmed/3918071; http://www.tandfonline.com/doi/full/10.1080/21548331.1985.11702995; https://dx.doi.org/10.1080/21548331.1985.11702995; https://www.tandfonline.com/doi/abs/10.1080/21548331.1985.11702995
Informa UK Limited
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