The diagnosis of idiopathic pulmonary fibrosis: current and future approaches

Fernando J Martinez, Alison Chisholm, Harold R Collard et al

Lancet Respir Med. 2017, vol 5(1): 61–71

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Idiopathic pulmonary fibrosis in Switzerlands: diagnosis and treatment

Position paper of the Swiss Working Group for Interstitial and Rare Lung Diseases of the Swiss Respiratory Society

M Funke-Chambour, A Azzola, D Adler et al

Respiration 2017, vol 93: 363-378

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Oxigenoterapia de alto fluxo nasal em pacientes com fibrose pulmonary idiopática sob cuidados paliativos: relato de um caso

F S L Silva, P H Barreto, R S de Vasconcelos et al

Rev Med UFC 2017, vol 57 (1): 69-72

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Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen

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BMC Pulm Med. 2017; vol 17: 154

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Recents advances in managing idiopathic pulmonary fibrosis

C Scelfo, A Caminati, S Harari

Version 1, F1000Res 2017, vol 6: 2052

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Fibrose pulmonar idiopática no Brasil: desafios para caracterização epidemiológica e abordagem

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Mortalidade por fibrose pulmonar idiopática: análise temporal no Brasil, 1979-2014

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Caracterización clínica, serológica y patrón radiológico de una cohorte unicéntrica de pacientes con enfermedad pulmonar difusa

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Pirfenidone safety and adverse event management in idiopathic pulmonary fibrosis

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European Respiratory Review 26 (146): 170057

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Pharmacotherapy for idiopathic pulmonary fibrosis: current landscape and future potential

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Severe idiopathic pulmonary fibrosis: What can be done?

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Recent lessons learned in the management of acute exacerbations of idiopathic pulmonary fibrosis

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Overview of idiopathic pulmonary fibrosis (IPF) and evidence-based guidelines

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Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis

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BMC Pulm Med. 2017; 17: 152

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Idiopathic pulmonary fibrosis: a genetic disease that involves mucociliary dysfunction of the peripheral airways

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Comorbid conditions in idiopathic pulmonary fibrosis: recognition and management

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Front Med (Lausanne) 2017; vol 4: 12

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Role of microbial agents in pulmonary fibrosis

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Informal caregivers experience of supplemental oxygen in pulmonary fibrosis

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Pulmonary hypertension associated with idiopathic pulmonary fibrosis: current and future perspectives

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The processes and mechanisms of cardiac and pulmonary fibrosis

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Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study

Richard J Allen, Joanne Porte, Rebecca Braybrooke et al

Lancet Respir Med. 2017, vol 5(11): 869–880

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Genetics in idiopathic pulmonary fibrosis pathogenesis, prognosis and treatment

Amarpreet Kaur, Susan K. Mathai, David A. Schwartz

Front Med (Lausanne) 2017; vol 4: 154

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Pulmonary fibrosis: tissue characterization using late-enhanced MRI compared with unenhanced anatomic high-resolution CT

Lisa P. Lavelle, Darragh Brady, Sinead McEvoy et al

Diagn Interv Radiol. 2017 , vol 23(2): 106–111

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Identification and validation of differentially expressed transcripts by RNA-sequencing of formalin-fixed, paraffin-embedded (FFPE) lung tissue from patiens with idiopathic pulmonary fibrosis

Milica Vukmirovic, Jose D. Herazo-Maya, John Blackmon et al

BMC Pulm Med. 2017; 17: 15

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Pulmonary oxygen uptake and muscle deoxygenation kinetics during heavy intensity cycling exercise in patiens with emphysema and idiopathic pulmonary fibrosis

Melitta A. McNarry, Nicholas K. Harrison, Tom Withers et al

BMC Pulm Med. 2017; 17: 26.

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Mechanical ventilation in idiopathic pulmonary fibrosis: a nationwide analysis of ventilator use, outcomes, and resource burden

Joshua J. Mooney, Karina Raimundo, Eunice Chang, Michael S. Broder

BMC Pulm Med. 2017; 17: 84

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Azithromycin for idiopathic acute exacerbation of idiopathic pulmonary fibrosis: a retrospective single-center study

Kodai Kawamura, Kazuya Ichikado, Yuko Yasuda et al

BMC Pulm Med. 2017; 17: 94.

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Prognosis and longitudinal changes of physical activity in idiopathic pulmonary fibrosis

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BMC Pulm Med. 2017; vol 17: 104

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Unmet needs in the treatment of idiopathic pulmonary fibrosis – insights from patient chart review in five European countries

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BMC Pulm Med. 2017; 17: 124.

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Rev. chil. enferm. respir., Mar 2016, vol.32, no.1, p.13-17

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Trasplante pulmonar en pacientes portadores de fibrosis pulmonar: caracterización de una cohorte de 87 pacientes

Parada C, María Teresa et al

Rev. chil. enferm. respir., Dic 2015, vol.31, no.4, p.189-194

https://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-73482015000400002&lng=es&nrm=iso

 

Pulmonary fibrosis: pathogenesis, etiology and regulation

M S Wilson, T A Wynn

Mucosal Immunol 2009, vol 2 (2): 103-121

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2675823/

 

■ by Dr Paulo Fernando Leite

Cardiologia – Centro Médico Unimed BH

Rua Gonçalves Dias 202

Belo Horizonte/MG/Brasil

31 30033306       /   40204020

CRMMG: 7026

Email: pfleite1873@gmail.com