MYRIAN
ABURTO BARRENECHEA
PROFESORADO ASOCIADO
Publicaciones (41) Publicaciones de MYRIAN ABURTO BARRENECHEA
2024
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Influence of Clinical Practice Guidelines on the Diagnosis and Treatment of Idiopathic Pulmonary Fibrosis. Data from the Registry of the Spanish Society of Pulmonology and Thoracic Surgery
Open Respiratory Archives, Vol. 6, Núm. 3
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Influence of physical activity on the prognosis of COPD patients: the HADO.2 score – health, activity, dyspnoea and obstruction
ERJ Open Research, Vol. 10, Núm. 1
2023
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Change in physical activity related to admission for exacerbation in COPD patients
Respiratory Medicine, Vol. 212
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Impact of COVID-19 Infection on Patients with Preexisting Interstitial Lung Disease: A Spanish Multicentre Study
Archivos de Bronconeumologia, Vol. 59, Núm. 4, pp. 273-276
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Screening criteria for interstitial lung disease associated to rheumatoid arthritis: Expert proposal based on Delphi methodology
Reumatologia Clinica, Vol. 19, Núm. 2, pp. 74-81
2022
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Changes in health-related quality of life as a marker in the prognosis in COPD patients
ERJ Open Research, Vol. 8, Núm. 1
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Different Faces of Idiopathic Pulmonary Fibrosis With Preserved Forced Vital Capacity
Archivos de Bronconeumologia, Vol. 58, Núm. 2, pp. 135-141
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SER-SEPAR recommendations for the management of rheumatoid arthritis-related interstitial lung disease. Part 1: Epidemiology, risk factors and prognosis
Reumatologia Clinica, Vol. 18, Núm. 8, pp. 443-452
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SER-SEPAR recommendations for the the management of rheumatoid arthritis-related interstitial lung disease. Part 2: Treatment
Reumatologia Clinica, Vol. 18, Núm. 9, pp. 501-512
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Screening of interstitial lung disease in patients with rheumatoid arthritis: A systematic review
Reumatologia Clinica, Vol. 18, Núm. 10, pp. 587-596
2021
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Checking Siblings of Patients with Idiopathic Pulmonary Fibrosis as a Scheme for Early Disease Detection
Annals of the American Thoracic Society
2020
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Complications and hospital admission in the following 90 days after lung cryobiopsy performed in interstitial lung disease
Respiratory Medicine, Vol. 165
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Nintedanib in patients with progressive fibrosing interstitial lung diseases—subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised, double-blind, placebo-controlled, parallel-group trial
The Lancet Respiratory Medicine, Vol. 8, Núm. 5, pp. 453-460
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Predictive factors over time of health-related quality of life in COPD patients
Respiratory research, Vol. 21, Núm. 1, pp. 138
2019
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Biomarkers of extracellular matrix turnover in patients with idiopathic pulmonary fibrosis given nintedanib (INMARK study): a randomised, placebo-controlled study
The Lancet Respiratory Medicine, Vol. 7, Núm. 9, pp. 771-779
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COPD classification models and mortality prediction capacity
International Journal of COPD, Vol. 14, pp. 605-613
2018
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Diagnosis of Idiopathic Pulmonary Fibrosis: Differential Diagnosis
Medical sciences (Basel, Switzerland), Vol. 6, Núm. 3
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Importance of early diagnosis and treatment in idiopathic pulmonary fibrosis
Expert Review of Respiratory Medicine
2016
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Chronic obstructive pulmonary disease subtypes. transitions over time
PLoS ONE, Vol. 11, Núm. 9
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Noninvasive ventilation for severely acidotic patients in respiratory intermediate care units: Precision medicine in intermediate care units
BMC Pulmonary Medicine, Vol. 16, Núm. 1