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Annals of the American Thoracic Society
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October 30, 2020
Registries for Idiopathic Pulmonary Fibrosis: When Is It Time to Go Global?
Manuela Funke-Chambour
Therapeutische Umschau. Revue Therapeutique
|
February 18, 2016
[Anti-fibrotics as novel therapy for idiopathic pulmonary fibrosis]
Manuela Funke-Chambour, Thomas Geiser
Respiration; International Review of Thoracic Diseases
|
November 20, 2018
Antifibrotics: Shrinking the Box of Therapeutic Uncertainty
Sabina A Guler, Manuela Funke-Chambour
Praxis
|
September 7, 2017
Anke Schertel, Manuela Funke-Chambour, Thomas Geiser
Therapeutische Umschau. Revue Therapeutique
|
January 9, 2020
[Diagnostics of interstitial lung diseases in the multidisciplinary team]
Sabina Berezowska, Alexander Pöllinger, Manuela Funke-Chambour
Der Pathologe
|
January 30, 2020
[Idiopathic pulmonary fibrosis-epidemiology, causes, and clinical course]
Stephan C Schäfer, Manuela Funke-Chambour, Sabina Berezowska
JAMA
|
September 12, 2023
Ziritaxestat and Lung Function in Idiopathic Pulmonary Fibrosis
Leticia Kawano-Dourado, Manuela Funke-Chambour, Athol U Wells
Respiratory Research
|
January 28, 2025
Fibrosis in PCLS: comparing TGF-β and fibrotic cocktail
Carlos Machahua, Thomas M Marti, Patrick Dorn, et al.
Respiratory Research
|
November 15, 2017
Novel insights in cough and breathing patterns of patients with idiopathic pulmonary fibrosis performing repeated 24-hour-respiratory polygraphies
Anke Schertel, Manuela Funke-Chambour, Thomas Geiser, et al.
Der Pathologe
|
December 21, 2019
[The multidisciplinary discussion-the gold standard in diagnosing interstitial lung diseases]
Sabina Berezowska, Manuela Funke-Chambour, Alexander Pöllinger, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 62) with videos related to
Sort By:
Page
of 7
Annals of the American Thoracic Society
|
October 30, 2020
Registries for Idiopathic Pulmonary Fibrosis: When Is It Time to Go Global?
Manuela Funke-Chambour
Therapeutische Umschau. Revue Therapeutique
|
February 18, 2016
[Anti-fibrotics as novel therapy for idiopathic pulmonary fibrosis]
Manuela Funke-Chambour, Thomas Geiser
Respiration; International Review of Thoracic Diseases
|
November 20, 2018
Antifibrotics: Shrinking the Box of Therapeutic Uncertainty
Sabina A Guler, Manuela Funke-Chambour
Praxis
|
September 7, 2017
Anke Schertel, Manuela Funke-Chambour, Thomas Geiser
Therapeutische Umschau. Revue Therapeutique
|
January 9, 2020
[Diagnostics of interstitial lung diseases in the multidisciplinary team]
Sabina Berezowska, Alexander Pöllinger, Manuela Funke-Chambour
Der Pathologe
|
January 30, 2020
[Idiopathic pulmonary fibrosis-epidemiology, causes, and clinical course]
Stephan C Schäfer, Manuela Funke-Chambour, Sabina Berezowska
JAMA
|
September 12, 2023
Ziritaxestat and Lung Function in Idiopathic Pulmonary Fibrosis
Leticia Kawano-Dourado, Manuela Funke-Chambour, Athol U Wells
Respiratory Research
|
January 28, 2025
Fibrosis in PCLS: comparing TGF-β and fibrotic cocktail
Carlos Machahua, Thomas M Marti, Patrick Dorn, et al.
Respiratory Research
|
November 15, 2017
Novel insights in cough and breathing patterns of patients with idiopathic pulmonary fibrosis performing repeated 24-hour-respiratory polygraphies
Anke Schertel, Manuela Funke-Chambour, Thomas Geiser, et al.
Der Pathologe
|
December 21, 2019
[The multidisciplinary discussion-the gold standard in diagnosing interstitial lung diseases]
Sabina Berezowska, Manuela Funke-Chambour, Alexander Pöllinger, et al.
Page
of 7