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In MEDLINE/PubMed, every journal article is indexed with about 10–15 subject headings, subheadings and supplementary concept records, with some of them designated as major and marked with an asterisk, indicating the article's major topics. When performing a MEDLINE search via PubMed, entry terms are automatically translated into (i.e., mapped ...
The widespread use and acceptance of the Library of Congress Subject Headings facilitates the uniform access to and retrieval of items in libraries across the world; users can use the same search strategy and LCSH thesaurus, if the correct headings have been applied to the item by the library. Some LCSH decisions are achieved by extensive ...
An abstract is a brief summary of a research article, thesis, review, conference proceeding, or any in-depth analysis of a particular subject and is often used to help the reader quickly ascertain the paper's purpose. [1]
When it is useful to sub-divide these sections (for example, to separate a list of magazine articles from a list of books), this should be done using level 3 headings (===Books===) instead of definition list headings (;Books), as explained in the accessibility guidelines.
The Mendeley research catalog is a crowdsourced database of research documents. Researchers have uploaded nearly 100M documents into the catalog with additional contributions coming directly from subject repositories like Pubmed Central and Arxiv.org or web crawls. Free Mendeley [98] Merck Index: Chemistry, Biology, Pharmacology: Also available ...
Depending on the complexity or length of the text, the table of contents will include the parts (groups of chapters), if applicable, chapters or section headings, and sometimes chapter or section subheadings. [4] Formal reports (ten or more pages and being too long to put into a memo or letter) also have a table of contents.
The aim of the PRISMA statement is to help authors improve the reporting of systematic reviews and meta-analyses. [3] PRISMA has mainly focused on systematic reviews and meta-analysis of randomized trials, but it can also be used as a basis for reporting reviews of other types of research (e.g., diagnostic studies, observational studies).
Detailed subheadings for each module are specified for all jurisdictions. The contents of Module 1 and certain subheadings of others differ based on national requirements. However, investigational new drugs meant for emergency use or treatment applications and not for commercial distribution are not subject to the CTD requirements. [5] [6]