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Patient Registry Data for Research: A Basic Practical Guide

Mohamad Adam Bujang

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  "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": [
  "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": [
      "family": "Mohamad Adam Bujang"
  "publisher_place": "Kuala Lumpur, Malaysia", 
  "type": "book", 
  "id": "4722674"
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