Importance of an International Registry for and Collaborative Research on Esophageal Atresia

Esophageal atresia (EA) is a rare congenital defect. Data on EA prevalence, management, and long-term outcome are lacking because the available data come from small retrospective series from tertiary referral centers. An international multicenter registry would provide strong epidemiological data fr...

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Autors principals:	Frédéric Gottrand, Delphine Ley, Laurent Michaud, Rony Sfeir
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2017-04-01
Col·lecció:	Frontiers in Pediatrics
Matèries:	esophageal atresia congenital defect international registry population-based cohort collaborative research
Accés en línia:	http://journal.frontiersin.org/article/10.3389/fped.2017.00081/full
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