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Patient Registry Data for Research: A Basic Practical Guide

Mohamad Adam Bujang


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    <dct:title>Patient Registry Data for Research: A Basic Practical Guide</dct:title>
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    <dct:issued rdf:datatype="http://www.w3.org/2001/XMLSchema#gYear">2021</dct:issued>
    <dcat:keyword>Patient Registry</dcat:keyword>
    <dcat:keyword>Disease Registry</dcat:keyword>
    <dcat:keyword>Clinical Research</dcat:keyword>
    <dcat:keyword>Medical Registry</dcat:keyword>
    <dcat:keyword>Research Data</dcat:keyword>
    <dcat:keyword>Biostatistics</dcat:keyword>
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    <dct:description>&lt;p&gt;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.&lt;/p&gt;</dct:description>
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