Latin American Registry of Idiopathic Pulmonary Fibrosis (REFIPI): Clinical Characteristics, Evolution and Treatment.
暂无分享,去创建一个
M. Mejía | R. Kairalla | I. Buendía-Roldán | F. Caro | M. L. Alberti | J. Enghelmayer | M. Fernández | M. Selman | M. Florenzano | G. Arbo | Á. Undurraga | S. Auteri | P. Curbelo | C. Matiz | G. Tabaj | B. Varela | Y. Liberato | Fernando Guillén | J. L. Velazquez | L. Noriega-Aguirre | A. Amaral | Aníbal Bermúdez | Manuel de Jesús Díaz Verduzco | Isabel De la Fuente | Viviana Moyano | Alfredo Pachas | Silvia V. Escotorin | Esther Tavera | A. Pachas
[1] S. Aldhaheri,et al. Fine crackles on chest auscultation in the early diagnosis of idiopathic pulmonary fibrosis: a prospective cohort study , 2021, BMJ Open Respiratory Research.
[2] D. Lynch,et al. Diagnosis and Evaluation of Hypersensitivity Pneumonitis: CHEST Guideline and Expert Panel Report - Executive Summary. , 2021, Chest.
[3] N. Inui,et al. Cluster analysis-based clinical phenotypes of idiopathic interstitial pneumonias: associations with acute exacerbation and overall survival , 2020, BMC Pulmonary Medicine.
[4] W. Travis,et al. Diagnosis and Evaluation of Hypersensitivity Pneumonitis , 2021 .
[5] Ling Zhao,et al. Idiopathic Pulmonary Fibrosis Registry China study (PORTRAY): protocol for a prospective, multicentre registry study , 2020, BMJ Open.
[6] Jonathan H. Chung,et al. Diagnosis of Hypersensitivity Pneumonitis in Adults. An Official ATS/JRS/ALAT Clinical Practice Guideline , 2020, American journal of respiratory and critical care medicine.
[7] A. Prasse,et al. Survival and course of lung function in the presence or absence of antifibrotic treatment in patients with idiopathic pulmonary fibrosis: long-term results of the INSIGHTS-IPF registry , 2020, European Respiratory Journal.
[8] M. Kramer,et al. The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis , 2020, Respiratory Research.
[9] J. Soriano,et al. Demographic and clinical profile of idiopathic pulmonary fibrosis patients in Spain: the SEPAR National Registry , 2019, Respiratory Research.
[10] W. Seeger,et al. The European IPF registry (eurIPFreg): baseline characteristics and survival of patients with idiopathic pulmonary fibrosis , 2018, Respiratory Research.
[11] Z. Daniil,et al. Design, Rationale, Methodology, and Aims of a Greek Prospective Idiopathic Pulmonary Fibrosis Registry: Investigating Idiopathic Pulmonary Fibrosis in Greece (INDULGE IPF) , 2018, Respiration.
[12] A. Warth,et al. Real-World Experience with Nintedanib in Patients with Idiopathic Pulmonary Fibrosis , 2018, Respiration.
[13] D. Lynch,et al. Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper. , 2017, The Lancet. Respiratory medicine.
[14] G. Raghu,et al. Interstitial Lung Disease in India. Results of a Prospective Registry , 2017, American journal of respiratory and critical care medicine.
[15] J. Ryu. Faculty of 1000 evaluation for An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features. , 2016 .
[16] D. Lynch,et al. Acute Exacerbation of Idiopathic Pulmonary Fibrosis. An International Working Group Report. , 2016, American journal of respiratory and critical care medicine.
[17] Emily C. O'Brien,et al. Rationale for and design of the Idiopathic Pulmonary Fibrosis–PRospective Outcomes (IPF-PRO) registry , 2016, BMJ Open Respiratory Research.
[18] M. Sköld,et al. Idiopathic pulmonary fibrosis in Sweden: report from the first year of activity of the Swedish IPF-Registry , 2016, European clinical respiratory journal.
[19] D. Lynch,et al. An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features , 2015, European Respiratory Journal.
[20] Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis. , 2015, The New England journal of medicine.
[21] R. Wood‐Baker,et al. Australian Idiopathic Pulmonary Fibrosis Registry: Vital lessons from a national prospective collaborative project , 2014, Respirology.
[22] H. Collard,et al. A global registry for idiopathic pulmonary fibrosis: the time is now , 2014, European Respiratory Journal.
[23] Luca Richeldi,et al. Neglected evidence in idiopathic pulmonary fibrosis and the importance of early diagnosis and treatment , 2014, European Respiratory Review.
[24] J. Behr,et al. Investigating significant health trends in idiopathic pulmonary fibrosis (INSIGHTS-IPF): rationale, aims and design of a nationwide prospective registry , 2014, BMJ Open Respiratory Research.
[25] G. Raghu,et al. Chronic hypersensitivity pneumonitis in patients diagnosed with idiopathic pulmonary fibrosis: a prospective case-cohort study. , 2013, The Lancet. Respiratory medicine.
[26] J. Behr. Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosis. , 2012, The New England journal of medicine.
[27] E. Bagiella,et al. Delayed access and survival in idiopathic pulmonary fibrosis: a cohort study. , 2011, American journal of respiratory and critical care medicine.
[28] Luca Richeldi,et al. Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis. , 2011, The New England journal of medicine.
[29] Takeshi Johkoh,et al. American Thoracic Society Documents An Official ATS / ERS / JRS / ALAT Statement : Idiopathic Pulmonary Fibrosis : Evidence-based Guidelines for Diagnosis and Management , 2011 .