Reassessment of the Classification of the Severity in Idiopathic Pulmonary Fibrosis Using SF-36 Questionnaire

Internal Medicine - Japan
doi 10.2169/internalmedicine.44.196
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Japanese Society of Internal Medicine

Related search

Health-Related Quality of Life of Patients With Cystic Fibrosis Assessed by the SF-36 Questionnaire

Pneumonologia i Alergologia Polska
2013English

Use of the Sf-36 Questionnaire in Assessment of Quality of Life in Patients With Chronic Thromboembolic Pulmonary Hypertension

The Clinician
2018English

The SF 36 Health Survey Questionnaire. Unanswered Questions Remain.

BMJ
1993English

The Pathogenesis of Idiopathic Pulmonary Fibrosis

Therapeutic Advances in Respiratory Disease
PulmonaryRespiratory MedicinePharmacology
2010English

The Timed Walk Test as a Measure of Severity and Survival in Idiopathic Pulmonary Fibrosis

European Respiratory Journal
MedicinePulmonaryRespiratory Medicine
2005English

Increased Activated Regulatory T Cells Proportion Correlate With the Severity of Idiopathic Pulmonary Fibrosis

Respiratory Research
PulmonaryRespiratory Medicine
2017English

The Genetic Basis of Idiopathic Pulmonary Fibrosis

European Respiratory Journal
MedicinePulmonaryRespiratory Medicine
2015English

Advances in the Management of Idiopathic Pulmonary Fibrosis

F1000 Medicine Reports
2010English

Idiopathic Pulmonary Fibrosis

Pulmonologiya
PulmonaryRespiratory Medicine
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy