Interpretation of the guidelines for clinical diagnosis of idiopathic pulmonary fibrosis in 2018 / 中国实用内科杂志
Chinese Journal of Practical Internal Medicine
;
(12): 431-436, 2019.
Artículo
en Chino
| WPRIM
| ID: wpr-816039
ABSTRACT
Idiopathic pulmonary fibrosis(IPF) is a specific form of interstitial lung diseases(ILDs) with unknown causes. In 2018, the international expert panel of interstitial lung diseases updated the diagnostic criteria of IPF based on the imaging and histopathology published in 2011. We will interpret the new 2018 version of diagnostic guidelines for IPF.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Tipo de estudio:
Estudio diagnóstico
/
Guía de Práctica Clínica
Idioma:
Chino
Revista:
Chinese Journal of Practical Internal Medicine
Año:
2019
Tipo del documento:
Artículo
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