Quantification of Lung Fibrosis in IPF-Like Mouse Model and Pharmacological Response to Treatment by Micro-Computed Tomography

• Автори: Francesca Ruscitti (Автор), Francesca Ravanetti (Автор), Valeria Bertani (Автор), Luisa Ragionieri (Автор), Laura Mecozzi (Автор), Nicola Sverzellati (Автор), Mario Silva (Автор), Livia Ruffini (Автор), Valentina Menozzi (Автор), Maurizio Civelli (Автор), Gino Villetti (Автор), Franco Fabio Stellari (Автор)
• Формат: Книга
• Опубліковано: Frontiers Media S.A., 2020-07-01T00:00:00Z.
• Предмети: article
• Онлайн доступ: Connect to this object online.

Idiopathic pulmonary fibrosis (IPF) is a chronic progressive degenerative lung disease leading to respiratory failure and death. Although anti-fibrotic drugs are now available for treating IPF, their clinical efficacy is limited and lung transplantation remains the only modality to prolong survival...