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# Patient Registry Data for Research: A Basic Practical Guide

### Citation Style Language JSON Export

{
"publisher": "Institute for Clinical Research, NIH MY",
"DOI": "10.5281/zenodo.4722674",
"ISBN": "9781005767600",
"language": "eng",
"title": "Patient Registry Data for Research: A Basic Practical Guide",
"issued": {
"date-parts": [
[
2021,
4,
27
]
]
},
"abstract": "<p>Analysis of patient data can be a complicated and challenging process, especially when the data involve many subjects and many variables. A patient registry is a database that organizes collecting the important set of data on a list of identifiable individuals for a specific disease. This type of data usually has tons of data and hundreds of different variables. Thus, the approach to conducting research by using a patient registry database will be more complicated than the other types of dataset. Since the handling of patient registry data is a challenging task, the authors have come out with this book to become a guideline for the statisticians, medical officers and scientists for them to refer as a handbook whenever they need to use patient registry data for their research.</p>",
"author": [
{
}
],
"publisher_place": "Kuala Lumpur, Malaysia",
"type": "book",
"id": "4722674"
}
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