Importance of national and international registries of inborn errors of metabolism

In the subject of rare diseases, experience and knowledge is limited. With a rare disease registry, longitudinal data can be added to increase information of them and to improve the quality of medical care and the patient outcome. Registries, unlike randomized controlled trials, provide a source of...

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Bibliographic Details
Main Author: Roberto Giugliani
Format: Article
Language:Spanish
Published: Instituto Nacional de Pediatría 2014-07-01
Series:Acta Pediátrica de México
Subjects:
Online Access:http://ojs.actapediatrica.org.mx/index.php/APM/article/view/596