Spanish Registry of Patients With Alpha-1 Antitrypsin Deficiency: Database Evaluation and Population Analysis.

Beatriz Lara,Ignacio Blanco,María Teresa Martínez,Esther Rodríguez,Ana Bustamante,Francisco Casas,Sergio Cadenas,José M Hernández,Lourdes Lázaro,María Torres,Sergio Curi,Cristina Esquinas,Francisco Dasí,Amparo Escribano, Inés Herrero,Beatriz Martínez-Delgado,Francisco Javier Michel,Francisco Rodríguez-Frías,Marc Miravitlles

Archivos de Bronconeumología (English Edition)（2017）

引用 14|浏览56

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摘要

The REDAAT registry is a useful tool for obtaining quality information about this minority disease in routine clinical practice conditions, although it is difficult to obtain follow-up data, and the representativeness of the sample included cannot be determined.

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关键词

Registry,Alpha-1 antitripsin

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