Elsevier Author Aid Human Diseases Collection, part 1 (showcase)
-> The Human Disease Author Aid Collection combines information about rare and common diseases in standardized, easy-to-navigate overviews and tables. -> The Author Aid Collection includes clinical, molecular, and pharmacological data from several Elsevier and public sources. -> Author Aid Templates can be a helpful guide for authors, researchers, clinicians, and students, especially those interested in rare diseases, because they highlight the latest updates, findings, and basic disease information from several sources on one page. Contents -> The Human Disease Author Aid Collection is published in parts with 5-10 diseases grouped by therapeutic areas, except Part 1. Tables are planned to be updated with the latest metadata and citations quarterly. -> Part 1 includes opening examples for common and rare human diseases: hemophilia, phenylketonuria, alpha-1 antitrypsin deficiency, migraine, and COVID-19. -> Each disease template overview in Part 1 includes six sections: Terminology; Epidemiology/Demographics; Clinical presentation/Diagnosis; Etiology/Pathology (genetics, biomarkers, pathways); Treatment/Follow-Up; and Case studies. Each subset of data is linked to a list of publications with relevant citations.
Steps to reproduce
Automatic excerption followed by manual curation is used to generate the templates. Automatic information excerption is powered by Elsevier Natural Language Processing technology, products, and public sources (ClinicalKey & EMMET, Pathway Studio, Pharmapendium, Elsevier Text Mining, Embase, Science Direct, Orphanet, ClinicalTrials, PubMed, and others).
Additional metadata for Elsevier datasets
|Date the data was collected||2020-11-01T17:00:00.000Z|